L-Glutamine

L-glutamine structural formula

Structural formula

Business number 017Z
Molecular formula C5H10N2O3
Molecular weight 146.15
label

L-Glutamic acid-5-amide,

L-aminocarbonylbutyrine,

L-2-Aminoglutaric acid amide,

(S)-(+)-Glutamine,

L-Glutamic acid 5-amide,

amino acid drugs,

intermediates,

Biochemical reagents

Numbering system

CAS number:56-85-9

MDL number:MFCD00008044

EINECS number:200-292-1

RTECS number:MA2275100

BRN number:1723797

PubChem number:24277983

Physical property data

1. Properties: colorless needle-like crystals

2. Density (g/mL, 25/4℃): 1.321

3. Relative vapor density (g/mL , air=1): Undetermined

4. Melting point (ºC, decomposition): 185~186

5. Boiling point (ºC, normal pressure): 185

6. Boiling point (ºC, 5.2kPa): Undetermined

7. Refractive index: Undetermined

8. Flash point (ºC): Undetermined

9. Specific rotation (º): 32.25° (c=10, 2 N HCl).

10. Autoignition point or ignition temperature (ºC): Undetermined

11. Vapor pressure (kPa, 25ºC): Undetermined

12. Saturation Vapor pressure (kPa, 60ºC): Undetermined

13. Heat of combustion (KJ/mol): Undetermined

14. Critical temperature (ºC): Undetermined

15. Critical pressure (KPa): Undetermined

16. Log value of oil-water (octanol/water) partition coefficient: Undetermined

17. Explosion upper limit (% , V/V): Undetermined

18. Lower explosion limit (%, V/V): Undetermined

19. Solubility: soluble in water, almost insoluble in methanol, Ethanol, ether, benzene, acetone, ethyl acetate and chloroform, etc.

Toxicological data

1. Acute toxicity: Men’s oral TDLo: 27mg/kg/1W-I; Rat’s oral LD50: 7500mg/kg; Mice’s oral LD50: 21700mg/kg 2. Other multi-dose toxicity: Rat’s oral TDLo: 260mg/kg/30D-I 3. Mutagenicity: sister chromatids exchangeTEST system: human lymphocytes: 10mg/L

Ecological data

None

Molecular structure data

1. Molar refractive index:33.83

2. Molar volume (cm3/mol): 110.5

3. Isotonic specific volume (90.2K): 313.3

4. Surface tension (dyne/cm): 64.5

5. Polarizability (10-24cm3): 13.41

Compute chemical data

1. Reference value for hydrophobic parameter calculation (XlogP): -3.1

2. Number of hydrogen bond donors: 3

3. Number of hydrogen bond acceptors: 4

4. Number of rotatable chemical bonds: 4

5. Number of tautomers: 2

6. Topological molecular polar surface area (TPSA): 106

7. Number of heavy atoms: 10

8. Surface charge: 0

9. Complexity: 146

10. Isotopes Number of atoms: 0

11. Determine the number of atomic stereocenters: 1

12. Uncertain number of atomic stereocenters: 0

13. Determine chemical bonds Number of stereocenters: 0

14. Number of stereocenters of uncertain chemical bonds: 0

15. Number of covalent bond units: 1

Properties and stability

1. Participate in the biosynthesis of glucosamine, a component of mucin in the digestive tract mucosa, thereby promoting the repair of mucosal epithelial tissue and helping to eliminate ulcer lesions. At the same time, it can promote brain metabolism and improve brain function through the blood-brain barrier. Like glutamate, it is an important nutrient for brain metabolism.

2. Exist in tobacco leaves and smoke.

3. Valuable in the field of immunity. After the body converts toxic ammonia into non-toxic glutamine, it is excreted through urine. Generally not involved in the composition of proteins.

Storage method

This product should be stored in a sealed, cool place and away from light.

Synthesis method

L-Glutamine widely exists in nature. For example, it is contained in free state in pumpkin and sunflower seedlings, and its N-ethyl compound (theanine) is contained in tea leaves. Although glutamine can be extracted from natural products, fermentation and synthesis are used for mass production. 1. Synthesis method: It is obtained by condensation, addition, salt formation and hydrolysis of L-glutamic acid-5-methyl ester ([1499-55-4]). Glutamic acid is esterified with methanol in the presence of concentrated sulfuric acid, and the resulting esterified liquid is added dropwise to the mixture of methanol and carbon disulfide. While adding dropwise, ammonia is circulated under cooling. After the esterification liquid is added dropwise, continue to pass ammonia, then add triethylamine, and leave it sealed at 30°C for 40 hours. After concentrating under reduced pressure to drive out ammonia, a concentrated solution of γ-methyl ester-L-glutamic acid-N-amino acid diammonium salt was obtained. Heat it to 40-45°C and add acetic acid. After stirring for 30 minutes, carbon disulfide was removed under reduced pressure, and a large amount of crystals precipitated. Then add an equal volume of methanol, place it at 0°C for 12 hours, and filter to obtain crude glutamine. The finished product is obtained through activated carbon decolorization and recrystallization. 2. Fermentation method uses glucose, acetic acid, and ethanol as the carbon source of the culture medium, and uses Brevibacterium flavum for fermentation. The yield based on glucose is 39g/L, and the yield is 39%.

2.Synthesis

3.Fermentation method

4. Extracted from the cell wall of fungi.

Purpose

1. This product is converted into sugar amine in the body, which serves as a precursor for mucin synthesis and can promote ulcer healing. It is mainly used as a peptic tract ulcer drug. In addition, it can also be used as a brain function improver and in the treatment of alcoholism.

2.It is used to improve the brain function of children with mental retardation and patients with mental disorders, alcoholism and epilepsy.

3. Nutritional supplements. In medicine, it is used to treat digestive organ ulcers (gastric ulcers, duodenal ulcers) and acute and chronic gastritis. It is also used as a brain function improver and to treat alcoholism.

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2-methoxy-4-nitroaniline

2-methoxy-4-nitroaniline structural formula

Structural formula

Business number 02C9
Molecular formula C7H8N2O3
Molecular weight 168.15
label

Red base B,

red bass B,

1-Amino-2-methoxy-4-nitrobenzene,

4-Nitro-o-anisidine

Numbering system

CAS number:97-52-9

MDL number:MFCD00007363

EINECS number:202-588-6

RTECS number:BZ7170000

BRN number:879619

PubChem number:24846314

Physical property data

  1. Appearance: yellow or tan powder
  2. Density (g/mL, 20℃): 1.2112
  3. Relative vapor density (g/mL , air = 1): not determined
  4. Melting point (ºC): 137-140
  5. Boiling point (ºC, normal pressure): not determined
  6. Boiling point (ºC , KPa): not determined
  7. Refractive index: not determined
  8. Flash point (ºC): not determined
  9. Specific rotation (º): not determined
  10. Autoignition point or ignition temperature (ºC): Not determined
  11. Vapor pressure (mmHg, 20.2ºC): Not determined
  12. Saturation vapor pressure (kPa, ºC ): Undetermined
  13. Heat of combustion (KJ/mol): Undetermined
  14. Critical temperature (ºC): Undetermined
  15. Critical pressure (KPa): Undetermined Determined
  16. Log value of oil-water (octanol/water) partition coefficient: Undetermined
  17. Explosion upper limit (%, V/V): Undetermined
  18. Explosion Lower limit (%, V/V): Undetermined
  19. Solubility: Insoluble in water, easily soluble in acetone, soluble in ethanol, ethyl acetate, acetic acid and benzene.

Toxicological data

Acute toxicity: rat oral LD50: 997mg/kg

Ecological data

This substance is harmful to the environment. Do not let this substance enter the environment.

Molecular structure data

1. Molar refractive index: 43.71

2. Molar volume (cm3/mol): 127.5

3. Isotonic specific volume (90.2K ): 345.2

4. Surface tension (dyne/cm): 53.6

5. Polarizability (10-24cm3): 17.32

Compute chemical data

1. Reference value for hydrophobic parameter calculation (XlogP): None

2. Number of hydrogen bond donors: 1

3. Number of hydrogen bond acceptors: 4

4. Number of rotatable chemical bonds: 1

5. Number of tautomers: none

6. Topological molecule polar surface area 81.1

7. Number of heavy atoms: 12

8. Surface charge: 0

9. Complexity: 169

10. Number of isotope atoms: 0

11. Determine the number of atomic stereocenters: 0

12. Uncertain number of atomic stereocenters: 0

13. Determine the number of chemical bond stereocenters: 0

14. Number of uncertain chemical bond stereocenters: 0

15. Number of covalent bond units: 1

Properties and stability

Avoid contact with strong oxidants, acids, acid anhydrides, and acid chlorides.

Toxic, easily absorbed by the skin and poisoned, but quickly excreted from the urethra. Operators need to wear gloves, masks, and drink plenty of water. OriginalThe material anthranilate is highly toxic, and the maximum allowable concentration in the air is 0.5mg/m3.

Storage method

Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Protect from direct sunlight. The packaging is sealed. They should be stored separately from oxidants, acids, acid anhydrides and acid chlorides, and avoid mixed storage. Equipped with the appropriate variety and quantity of fire equipment. Suitable materials should be available in the storage area to contain spills.

Synthesis method

o-Methoxyaniline is condensed with p-toluenesulfonyl chloride in the presence of sodium carbonate to obtain N-p-toluenesulfonyl o-methoxyaniline, and then nitrated with nitric acid to obtain 4-nitro-2-methoxy-N- For p-toluenesulfonyl aniline, the nitrate is treated with dilute sulfuric acid and hydrolyzed to remove the p-toluenesulfonyl group to obtain the finished product. Add o-methoxyaniline and equimolar p-toluenesulfonyl chloride to water at 85°C, and add sodium carbonate to adjust the pH of the reaction solution to 8. After reaching the end of the reaction, cool to 60°C, adjust the pH to 6 with sulfuric acid, cool to 45°C, and filter to obtain N-p-toluenesulfonyl-o-methoxyaniline with a yield of 99%. Add chlorobenzene to the nitrification pot and put in the above condensation product. Stir and add sodium nitrite at 30-33°C, and then slowly add 82% nitric acid. The adding temperature does not exceed 50°C. Cool to 35°C in about 15 minutes, and then add the condensation product and nitric acid in proportion. The feeding time is 3.5 hours, and the reaction temperature is controlled at 35-45°C. After the addition is completed, react at 50°C for 1.5 hours. Cool to 30°C and filter. The filter cake is washed with chlorobenzene and water, and dried to obtain 4-nitro-2-methoxy-N-p-toluenesulfonylaniline with a yield of 85%. Add this nitrate to 82%-83% sulfuric acid at 78°C. After the addition is completed, keep it at 90°C for 2.5 hours. Dilute with water, add alkali to neutralize to pH 7.5, press filter at 30°C, wash with 5% soda ash solution and water, and dry to obtain 2-methoxy-4-nitroaniline with a yield of 95%. The obtained product is yellow or tan powder. Content (dry basis) ≥98%. Raw material consumption quota: o-methoxyaniline 960kg/t, p-toluenesulfonyl chloride 1540kg/t.

Purpose

Dye intermediates. It is mainly used as the color base for ice dyeing dyes, namely red base B. Used to prepare dyes such as light-fast bright yellow 10GC. It is mainly used for dyeing and printing color development of cotton, linen, silk and polyester fabrics. It is also used to produce fast pigments, maroon IB, golden, black and organic lemon yellow lamp pigments.

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Formaldehyde oxime

Formaldehyde oxime structural formula

Structural formula

Business number 01J4
Molecular formula CH3NO
Molecular weight 45.04
label

Formyl oxime aqueous solution,

Formaldehydeoxime,

Formaldoximesolution,

Methyleneamine N-oxide,

N-Hydroxymethyleneimine

Numbering system

CAS number:75-17-2

MDL number:MFCD00058969

EINECS number:200-845-7

RTECS number:LP9720000

BRN number:None

PubChem ID:None

Physical property data

1. Characteristics: pure product with extremely strong refractive index Colorless liquid.


2. Density (g/mL,25/4℃):1035


3. Relative vapor density (g/mL,AIR=1): Unsure


4. Melting point (ºC): Unsure


5. Boiling point (ºC,Normal pressure): Uncertain


6. Boiling point (ºC,5.2kPa): Unsure


7. fold�Rate: Uncertain


8. Flash Point (ºC): 25


9. Specific optical rotation (º): Unsure


10. Autoignition point or ignition temperature (ºC): Unsure


11. Vapor pressure (kPa,25ºC): Unsure


12. Saturated vapor pressure (kPa,60ºC): Unsure


13. Heat of combustion (KJ/mol): Unsure


14. Critical temperature (ºC): Unsure


15. Critical pressure (KPa): Unsure


16. Oil and water (octanol/Log value of the partition coefficient (water): Uncertain


17. Explosion limit (%,V/V): Not sure


18. Lower explosion limit (%,V/V): Unsure


19. Solubility: soluble in water and acid. Can become a water-insoluble polymer at room temperature.




Toxicological data

1, teratogenicity


E. coli: 10umol/plate

Ecological data

None

Molecular structure data

1. Molar refractive index:10.86


2. Molar volume (m3/mol):48.4


3. isotonic specific volume (90.2K):110.8


4. Surface Tension (dyne/cm):27.4


5. Polarizability10-24cm3): 4.30

Compute chemical data

1. Reference value for hydrophobic parameter calculation (XlogP): 1.5

2. Number of hydrogen bond donors: 1

3. Number of hydrogen bond acceptors: 2

4. Number of rotatable chemical bonds: 0

5. Number of tautomers: 2

6. Topological molecule polar surface area 32.6

7. Number of heavy atoms: 3

8. Surface charge: 0

9. Complexity: 12.3

10. Number of isotope atoms: 0

11. Determine the number of atomic stereocenters: 0

12. Uncertain number of atomic stereocenters: 0

13. Determine the number of chemical bond stereocenters: 0

14. Number of uncertain chemical bond stereocenters: 0

15. Number of covalent bond units: 1

Properties and stability

None

Storage method

This product should be kept sealed. Not suitable for long-term storage.

Synthesis method

None

Purpose

Used for determination of manganese, copper, nickel, cobalt and iron, etc.

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L-aspartic acid

L-aspartic acid structural formula

Structural formula

Business number 017Y
Molecular formula C4H7NO4
Molecular weight 133.1
label

L(+)-aminosuccinic acid,

L(+)-aminosuccinic acid,

L-aspartic acid,

L-aspartic acid,

(S)-(+)-Aminosuccinic acid,

(S)-Aspartic acid,

biochemical reagents,

Intermediates

Numbering system

CAS number:56-84-8

MDL number:MFCD00002616

EINECS number:200-291-6

RTECS number:CI9098500

BRN number:1723530

PubChem ID:None

Physical property data

1. Properties: Colorless orthorhombic leaf-shaped or rod-shaped crystals or crystalline powder, odorless. Often left-handed optical rotation.

2. Density (g/mL, 25/4℃): (d12.5/4) 1.514

3. Relative vapor density (g/mL, air=1) : Undetermined

4. Melting point (ºC): 270-271

5. Boiling point (ºC, normal pressure): Undetermined

6. Boiling point ( ºC, 5.2kPa): Not determined

7. Refractive index: Not determined

8. Flash point (ºC): Not determined

9. Specific optical rotation Degree (º): [a]20/D+25° (c=1.97, in 6mol/L hydrochloric acid).

10. Autoignition point or ignition temperature (ºC): Undetermined

11. Vapor pressure (kPa, 25ºC): Undetermined

12. Saturation Vapor pressure (kPa, 60ºC): Undetermined

13. Heat of combustion (KJ/mol): Undetermined

14. Critical temperature (ºC): Undetermined

15. Critical pressure (KPa): Undetermined

16. Log value of oil-water (octanol/water) partition coefficient: Undetermined

17. Explosion upper limit (% , V/V): Undetermined

18. Lower explosion limit (%, V/V): Undetermined

19. Solubility: soluble in hot water, acid, alkali and Salt solution, insoluble in ethanol and ether.

Toxicological data

1. Acute toxicity: mouse abdominal LC50: 6mg/kg

2. Other multiple dose toxicity: rat oral TDLo: 25079mg/kg/7D-C

3. Mutagenicity: sister chromatids exchangeTEST system: human lymphocytes: 10mg/L

Ecological data

None

Molecular structure data

1. Molar refractive index: 27.20

2. Molar volume (cm3/mol): 87.8

3. Isotonic specific volume (90.2K ): 261.3

4. Surface tension (dyne/cm): 78.2

5. Polarizability (10-24cm3): 10.78

Compute chemical data

1. Reference value for hydrophobic parameter calculation (XlogP): None

2. Number of hydrogen bond donors: 3

3. Number of hydrogen bond acceptors: 5

4. Number of rotatable chemical bonds: 3

5. Number of tautomers: none

6. Topological molecule polar surface area 101

7. Number of heavy atoms: 9

8. Surface charge: 0

9. Complexity: 133

10. Number of isotope atoms: 0

11. Determine the number of atomic stereocenters: 1

12. Uncertain number of atomic stereocenters: 0

13. Determine the number of chemical bond stereocenters: 0

14. Number of uncertain chemical bond stereocenters: 0

15. Number of covalent bond units: 1

Properties and stability

1. Stable properties under normal temperature and pressure.

2. It is a natural product and non-toxic.

3. Exist in tobacco leaves and smoke.

Storage method

Seal and store in a dry place.

Synthesis method

1. The preparation methods of L-aspartic acid include synthesis method and fermentation method. 1. The synthesis method mainly uses maleic acid or fumaric acid or their esters as raw materials, which are treated with ammonia under pressure and then hydrolyzed. It is relatively easy to synthesize racemic aspartic acid, but so far there is no ideal method to separate the racemate. 2. In the fermentation method, fumaric acid and ammonia are added under the action of enzymes to obtain products with high yields. This method only generates the left-handed form with high yield, so it is the main method for industrial production.

2. Obtained from fumaric acid and ammonia under the action of aspartase of Pseudomonas clover or Brevibacterium ammoniagenes.

3. Use maleic acid, fumaric acid or their esters as raw materials, and add ammonia under the action of enzymes. The reaction is as follows:

4. Tobacco: BU, 22; FC, 21.

Purpose

1. Biochemical and medical clinical research. It can be used as an ammonia detoxifier, liver function promoter, fatigue recovery agent and other pharmaceuticals. It can be used to make L-sodium aspartate food additives and additives for various refreshing drinks. It can also be used as biochemical reagents, culture media and organic synthesis intermediates.

2. Can be used as biochemical reagents, culture media and organic synthesis intermediates. In medicine, it is used as a component of heart disease drugs, liver function promoters, ammonia detoxifiers, fatigue relievers and amino acid infusions. It is also used as a preservative in the food industry.

3. Nutritional supplements. Add to various refreshing drinks. It is used medicinally as an ammonia detoxifier and liver function promoter. Used as nutritional additive in cosmetics.

4. L-aspartic acid is often used as a chiral substrate in diastereomeric alkylation reactions, and can be used as a chiral source to synthesize other chiral compounds.

Diastereoselective alkylation L-aspartate ester can be used in α– and β– Alkylation occurs (formula 1) [2], among which the β-alkylation reaction is the most widely used. During the β-alkylation reaction, the amino acid moiety has an important influence on the diastereoselectivity of the reaction. At the same time, β-dicarbonyl compounds can also be prepared through β-alkylation of cyclic derivatives of L-aspartic acid [3].

Synthesis of Chiral Compounds Using L-aspartic acid as the chiral source, a series of chiral compounds can be synthesized, such as using copper iodide After the action of sodium borohydride, etc., a multifunctional oxygen nitrogen heterocyclic compound (formula 2) can be obtained, which can further generate a quinoline compound [4].

Formation of amide bond L-aspartic acid, as an amino acid, is the same as other amino acids Amide compounds (formula 3)[5] can also be generated.

At the same time, you can also use L- Aspartic acid is used as the parent to realize the synthesis of cyclic lactam. For example, the synthesis of six-membered ring lactam (formula 4)[6]. The alkoxy group is also present in the product and therefore serves as an additional reaction site for further derivatization.

β Synthesis of amino acids (or amino acid esters) L-aspartic acid can generate β-amino acids or amino acid esters ( Formula 5)[10], this reaction realizes the conversion from natural amino acids to unnatural amino acids.

In addition, the L-aspartic acid molecule contains two carboxyl groups and one amino group, so it can be used as a multidentate ligand to coordinate with metal ions[7~9] Or form lactone compounds themselves[10,11].

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2,5-Dimethyl-1-phenylpyrrole

2,5-dimethyl-1-phenylpyrrole structural formula

Structural formula

Business number 01TG
Molecular formula C12H13N
Molecular weight 171.24
label

1-phenyl-2,5-dimethylpyrrole,

2,5-Dimethyl-1-phenyl-1H-pyrrole,

1-Phenyl-2,5-dimethylpyrrole

Numbering system

CAS number:83-24-9

MDL number:MFCD00022464

EINECS number:201-461-2

RTECS number:None

BRN number:124370

PubChem ID:None

Physical property data

1. Physical property data


1. Character: Uncertain


2. Density (g/mL,25/4℃): Unsure


3. Relative vapor density (g/ mL,air=1 ): Unsure


4. Melting point (ºC):50-51


5. Boiling point (ºC,Normal pressure):155-160


6. Boiling point (ºC,5.2kPa): Unsure


7. Refractive index: Uncertain


8. Flash Point (ºC): Unsure


9. Specific optical rotation (º): Unsure


10. Autoignition point or ignition temperature (ºC): Unsure


11. Vapor pressure (kPa,25ºC): Unsure


12. Saturation vapor pressure (kPa,60ºC): Unsure


13. Heat of combustion (KJ/mol): Unsure


14. Critical temperature (ºC): Unsure


15. Critical pressure (KPa): Unsure


16. Oil and water (octanol/Log value of the partition coefficient (water): Uncertain


17. Explosion limit ( %,V/V): Unsure


18. Lower explosion limit (%,V/V): Unsure


19. Solubility: Uncertain.

Toxicological data

None

Ecological data

None

Molecular structure data

5. Molecular property data:


1. Molar refractive index: 56.33


2. Molar volume (m3/mol):177.7


3. Isotonic specific volume (90.2K ): 427.1


4. Surface Tension (dyne/cm):33.3


5. Polarizability10-24cm3):22.33

Compute chemical data

1. Reference value for hydrophobic parameter calculation (XlogP): 3.1

2. Number of hydrogen bond donors: 0

3. Number of hydrogen bond acceptors: 0

4. Number of rotatable chemical bonds: 1

5. Number of tautomers: none

6. Topological molecule polar surface area 4.9

7. Number of heavy atoms: 13

8. Surface charge: 0

9. Complexity: 151

10. Number of isotope atoms: 0

11. Determine the number of atomic stereocenters: 0

12. Uncertain number of atomic stereocenters: 0

13. Determine the number of chemical bond stereocenters: 0

14. Number of uncertain chemical bond stereocenters: 0

15. Number of covalent bond units: 1

Properties and stability

None

Storage method

None

Synthesis method

None

Purpose

None

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Methyl magnesium bromide

Methyl magnesium bromide structural formula

Structural formula

Business number 01J3
Molecular formula CH3MgBr
Molecular weight 119.24
label

Grignard reagent,

format reagent

Numbering system

CAS number:75-16-1

MDL number:MFCD00000041

EINECS number:200-844-1

RTECS number:OM3700000

BRN number:3535220

PubChem number:24858252

Physical property data

1. Properties: Solid

2. Density (g/mL, 20℃): 1.035

3. Relative vapor density (g/mL, air=1): Undetermined

4. Melting point (ºC): Undetermined

5. Boiling point (ºC, normal pressure): Undetermined

6. Boiling point (ºC, 5.2kPa): Not determined

7. Refractive index: Not determined

8. Flash point (ºF): 77

9. Specific rotation (º ): Undetermined

10. Autoignition point or ignition temperature (ºC): 160

11. Vapor pressure (kPa, 25ºC): Undetermined

12. Saturated vapor pressure (kPa, 60ºC) not determined:

13. Heat of combustion (KJ/mol): not determined

14. Critical temperature (ºC): not determined

15. Critical pressure (KPa): Undetermined

16. Log value of oil-water (octanol/water) partition coefficient: Undetermined

17. Explosion Upper limit (%, V/V): Undetermined

18. Lower explosion limit (%, V/V): Undetermined

19. Solubility: Reacts strongly with water, producing Combustible gas

Toxicological data

None

Ecological data

None

Molecular structure data

None

Compute chemical data

1. Reference value for hydrophobic parameter calculation (XlogP): None

2. Number of hydrogen bond donors: 0

3. Number of hydrogen bond acceptors: 2

4. Number of rotatable chemical bonds: 0

5. Number of tautomers: none

6. Topological molecule polar surface area 0

7. Number of heavy atoms: 3

8. Surface charge: 0

9. Complexity: 4.8

10. Number of isotope atoms: 0

11. Determine the number of atomic stereocenters: 0

12. Uncertain number of atomic stereocenters: 0

13. Determine the number of chemical bond stereocenters: 0

14. Number of uncertain chemical bond stereocenters: 0

15. Number of covalent bond units: 3

Properties and stability

Reacts with water, oxides, acids, alkalis, and alcohols.

Sensitive to water, light and air.

Storage method

Store in a cool, dry, well-ventilated non-combustible warehouse. Keep away from fire and heat sources. The warehouse temperature should not exceed 28℃.The packaging must be sealed and must not come into contact with air. Keep away from light. Not suitable for large quantities or long-term storage. It should be stored separately from acids, flammables, combustibles, oxidants, oxygen, compressed air, etc. The lighting, ventilation and other facilities in the storage room should be explosion-proof, and the switches should be located outside the warehouse. Equipped with the appropriate variety and quantity of fire equipment. Fire and explosion prevention technical measures must be taken during tank storage. It is prohibited to use mechanical equipment and tools that are prone to sparks. When handling, load and unload with care to prevent damage to packaging and containers. Smoking, drinking, and eating are not allowed at the operation site.

Synthesis method

Use carbide tools to cut single crystal magnesium flakes with a purity of 99.999%, wash them several times with ether treated with lithium aluminum tetrahydride, and add a dry ice-acetone condenser tube. And in the reaction bottle directly connected to the ether distillation device. The device is repeatedly baked with gas lamps and filled with high-purity nitrogen several times. Add dry ice to the condenser tube, evaporate 50 mL of ether directly into the flask, and then introduce a small amount of ethyl bromide from the side tube installed near the bottom of the condenser tube. Bubbles are released and heat is released, proving that the reaction has begun. Thereafter, continue to pass in methyl bromide and steam into ether. Keep methyl bromide and ether at reflux without heating until the magnesium metal reacts completely. During this period, it is appropriate to keep the ether solution at about 300 mL. Remove the flask in the nitrogen flow and put it in the operating box with a stopper, filter it into the flask with a glass sand funnel, and cover it with a tetrafluoroethylene piston. A colorless and transparent methylmagnesium bromide solution was obtained. The ratio of the analytical values ​​of C:Mg:Br is 1.00:1.03:0.99.


Purpose

for organic synthesis

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5-nitrosalicylicaldehyde

5-Nitrosalicylicaldehyde structural formula

Structural formula

Business number 02C8
Molecular formula C7H5NO4
Molecular weight 167.12
label

2-hydroxy-5-nitrobenzoyl,

2-Hydroxy5-nitrobenzaldehyae

Numbering system

CAS number:97-51-8

MDL number:MFCD00007337

EINECS number:202-587-0

RTECS number:CU6675000

BRN number:512565

PubChem number:24856642

Physical property data

  1. Appearance: light yellow or white powder.
  2. Density (g/mL, 20℃): Undetermined
  3. Relative vapor density (g/mL, air=1): Undetermined
  4. Melting point ( ºC): 125-128
  5. Boiling point (ºC, normal pressure): Undetermined
  6. Boiling point (ºC, KPa): Undetermined
  7. Refractive index: Undetermined Determined
  8. Flash point (ºC): Not determined
  9. Specific optical rotation (º): Not determined
  10. Autoignition point or ignition temperature (ºC): Not determined Determined
  11. Vapor pressure (mmHg, 20.2ºC): Undetermined
  12. Saturation vapor pressure (kPa, ºC): Undetermined
  13. Heat of combustion (KJ/mol ): Undetermined
  14. Critical temperature (ºC): Undetermined
  15. Critical pressure (KPa): Undetermined
  16. Oil-water (octanol/water) partition coefficient Log value: Undetermined
  17. Upper explosion limit (%, V/V): Undetermined
  18. Lower explosion limit (%, V/V): Undetermined
  19. Solubility: Not determined

Toxicological data

Acute toxicity: Rat oral LD50: 799mg/kg; Mouse oral LD50: 672mg/kg;

Ecological data

None

Molecular structure data

1. Molar refractive index: 41.43

2. Molar volume (cm3/mol): 111.3

3. Isotonic specific volume (90.2K ): 322.8

4. Surface tension (dyne/cm): 70.5

5. Polarizability (10-24cm3): 16.42

Compute chemical data

1. Reference value for hydrophobic parameter calculation (XlogP): None

2. Number of hydrogen bond donors: 1

3. Number of hydrogen bond acceptors: 4

4. Number of rotatable chemical bonds: 1

5. Number of tautomers: 4

6. Topological molecule polar surface area 83.1

7. Number of heavy atoms: 12

8. Surface charge: 0

9. Complexity: 188

10. Number of isotope atoms: 0

11. Determine the number of atomic stereocenters: 0

12. Uncertain number of atomic stereocenters: 0

13. Determine the number of chemical bond stereocenters: 0

14. Number of uncertain chemical bond stereocenters: 0

15. Number of covalent bond units: 1

Properties and stability

None

Storage method

None

Synthesis method

None

Purpose

Intermediates for organic synthesis of medicines, spices and dyes.

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carbon disulfide

Carbon disulfide structural formula

Structural formula

Business number 01J2
Molecular formula CS2
Molecular weight 76.14
label

carbon disulfide,

Dithoicarbonic anhydride,

Carbon bisulfide,

Aliphatic sulfur compounds

Numbering system

CAS number:75-15-0

MDL number:MFCD00011321

EINECS number:200-843-6

RTECS number:FF6650000

BRN number:1098293

PubChem number:24860298

Physical property data

1. Properties: colorless or light yellow transparent liquid with pungent odor and easy to evaporate. [1]

2. Melting point (℃): -111.5[2]

3. Boiling point (℃): 46.3[3]

4. Relative density (water = 1): 1.26[4]

5. Relative vapor Density (air=1): 2.63[5]

6. Saturated vapor pressure (kPa): 40 (20℃)[6]

7. Heat of combustion (kJ/mol): -1029.4[7]

8. Critical temperature (℃): 280[8]

9. Critical pressure (MPa): 7.39[9]

10. Octanol/water partition coefficient: 1.94 [10]

11. Flash point (℃): -30 (CC) [11]

12. Ignition temperature ( ℃): 90[12]

13. Explosion upper limit (%): 50.0[13]

14. Explosion Lower limit (%): 1.3[14]

15. Solubility: Insoluble in water, soluble in most organic solvents such as ethanol and ether. [15]

16. Refractive index (25ºC): 1.6241

17. Viscosity (mPa·s, 20ºC): 0.363

18. Ignition point (ºC): 100

19. Heat of evaporation (KJ/mol, 25ºC): 27.54

20. Heat of fusion (KJ/mol): 4.392

p>

21. Heat of formation (KJ/mol): 89.47

22. Specific heat capacity (KJ/(kg·K), 25ºC, constant pressure): 1.00

23 .Conductivity (S/m, 25ºC): 3.7×10-3

Toxicological data

1. Acute toxicity[16] LD50: 3188mg/kg (rat oral)

2. Irritation No data yet

3. Subacute and chronic toxicity[17] Rabbit inhalation 1.28g/m3, 5 months, causing chronic poisoning; 0.5~0.6g/m3, 6.5 months, causing an increase in serum cholesterol.

4. Mutagenicity [18] Microbial mutagenicity: Salmonella typhimurium 100μg/dish. Sister chromatid exchange: human lymphocytes 10200μg/L

5. Teratogenicity [19] Inhalation is the lowest in rats 1 to 22 days after pregnancy Toxic dose (TCLo) 10mg/m3 (8h) can cause eye and ear development malformations. Rats inhaled the lowest toxic dose (TCLo) 100 mg/m3 (8 hours) from 1 to 21 days after pregnancy, causing developmental malformations of the craniofacial region (including nose and tongue).

6. Others[20] Minimum toxic concentration for male inhalation (TCLo): 40mg/m3 (91 weeks ), causing changes in sperm production. The lowest toxic concentration for inhalation in rats (TCLo): 100mg/m3 (8h) (administered from 1st to 21st day of pregnancy), �� Started with fetal death and abnormal craniofacial development.

Ecological data

1. Ecotoxicity[21] LC50: 162~135mg/L (24~96h) (mosquito fish)

2. Biodegradability No data yet

3. Non-biodegradability[22] In the air, when hydroxyl radicals When the concentration is 5.00×105 pieces/cm3, the degradation half-life is 5.5d (theoretical).

4. Bioaccumulation [23] BCF: <6.1 (carp, contact concentration 50μg/L) <60 (carp, contact concentration 5μg/L)

Molecular structure data

1. Molar refractive index: 21.50

2. Molar volume (cm3/mol): 60.4

3. Isotonic specific volume (90.2K ): 143.8

4. Surface tension (dyne/cm): 32.0

5. Polarizability (10-24cm3): 8.52

Compute chemical data

1. Reference value for hydrophobic parameter calculation (XlogP): 2.1

2. Number of hydrogen bond donors: 0

3. Number of hydrogen bond acceptors: 2

4. Number of rotatable chemical bonds: 0

5. Number of tautomers: none

6. Topological molecule polar surface area 64.2

7. Number of heavy atoms: 3

8. Surface charge: 0

9. Complexity: 18.3

10. Number of isotope atoms: 0

11. Determine the number of atomic stereocenters: 0

12. Uncertain number of atomic stereocenters: 0

13. Determine the number of chemical bond stereocenters: 0

14. Number of uncertain chemical bond stereocenters: 0

15. Number of covalent bond units: 1

Properties and stability

1. Extremely flammable and can easily burn and explode when exposed to heat, sparks, flames or oxidants. Decomposes when heated to produce toxic sulfide fumes. Reacts violently with aluminum, zinc, potassium, fluorine, chlorine, azide, etc., posing a risk of combustion and explosion. High-speed impact and friction can cause combustion and explosion due to static spark discharge.

2. Chemical properties: Stable to acids, and does not interact with concentrated sulfuric acid and concentrated nitric acid at room temperature. But it is unstable to alkali and reacts with potassium hydroxide to generate potassium thiosulfate and potassium carbonate. It reacts with sodium alcohol to form xanthate; it gradually oxidizes in the air, becoming yellow and smelly. It decomposes under the influence of sunlight; at low temperatures, it reacts with water to form crystals with the structure of 2CS2·H2O. It reacts with chlorine under appropriate conditions to produce carbon tetrachloride and sulfur chloride.

3. The high-concentration vapor of this product has an anesthetic effect. The concentration is 0.1% to 0.3%. Inhalation can cause death in 1 hour. Even if it is lower than the lethal dose, it will leave sequelae. Long-term inhalation (3 months) 160 When ×10-6 or more, neuritis will occur after 1 to 2 years. The maximum allowable concentration in the workplace is 60mg/m3. This product is toxic and irritating. Closed operation, local exhaust. Operators must undergo special training and strictly abide by operating procedures. It is recommended that operators wear self-priming filter gas masks (half masks), chemical safety glasses, anti-static overalls, and rubber oil-resistant gloves. Keep away from fire and heat sources. Smoking is strictly prohibited in the workplace. Use explosion-proof ventilation systems and equipment. Prevent vapors from leaking into the workplace air. Avoid contact with oxidants, amines, and alkali metals. The flow rate should be controlled during filling, and a grounding device should be installed to prevent the accumulation of static electricity. Equipped with corresponding varieties and quantities of fire-fighting equipment and leakage emergency treatment equipment. Empty containers may be harmful residues.

4. Due to its low boiling point, strong volatility and high toxicity, it is easily dispersed in the air during production and use, causing serious pollution and harm to the environment and human body. Carbon disulfide is a poison that damages nerves and blood vessels. When people are exposed to high concentrations of carbon disulfide, it has a paralyzing effect. If it lasts for a long time, the respiratory center may be paralyzed, resulting in loss of consciousness and death. At high concentrations, it can also be absorbed by human skin.

5. This product is a gas anesthetic. Its vapor has a strong irritating effect on the skin and eyes, and can easily cause dermatitis and burns. Acute poisoning begins to cause delirium, and later anesthesia, loss of consciousness, and even death from respiratory failure. Long-term inhalation of its vapor can cause symptoms such as weak stomach, insomnia, fatigue, loss of appetite, headache, dizziness, abnormal sensation, drop in blood pressure, trembling, stiffness of hands and feet, slow movement, salivation, sweating, memory loss and other symptoms. Mainly damages the nervous and cardiovascular systems. When the vapor concentration is 12440 mg/m3, death will occur in 30 to 60 minutes. TJ 36-79 stipulates that the maximum allowable concentration in workshop air is 10 mg/m3.

6. Stability[24] Stable

7. Incompatible substances[25] Strong oxidizing agent, aluminum

8. Conditions to avoid contact[26] Heating

9. Polymerization hazard[27] No polymerization

10. Decomposition products[28] Hydrogen chloride

Storage method

1. Storage precautions[29] It is easily volatile at room temperature, so the surface of the container can be covered with water. Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature should not exceed 29°C. Keep container tightly sealed. They should be stored separately from oxidants, amines, alkali metals, and food chemicals, and avoid mixed storage. Use explosion-proof lighting and ventilation facilities. It is prohibited to use mechanical equipment and tools that are prone to sparks. The storage area should be equipped with leakage emergency treatment equipmentequipment and suitable containment materials.

2. This product is packed in glass bottles and metal barrels (aluminum barrels, iron barrels, storage tanks) and protected by wooden boxes, and must be stored in In a warehouse constructed of non-combustible materials and with ground ventilation facilities, keep away from fire sources and avoid sunlight. In summer, cooling measures should be taken to keep storage below 17°C. There should be no electrical equipment or heating facilities near the warehouse, and lightning or static electricity must be prevented from igniting fires. The liquid level of the storage tank should be sealed with inert gas. Store and transport according to regulations for flammable materials.

Synthesis method

1. Methane sulfur method: solid sulfur is heated and melted into liquid, and then purified with activated clay. Natural gas purification treatment uses light diesel to adsorb fractions above C2 and separate pure methane gas. After the natural gas and sulfur vapor are heated, they can be fully mixed and heated to 650°C, and then sent to the reactor for reaction. The pressurized partial condensation method is used to separate carbon disulfide and hydrogen sulfide, and carbon disulfide is obtained after distillation. The reaction formula is as follows:

2. Charcoal sulfur method : According to different heating methods, it can be divided into two categories: external heating iron steamer method and internal heating electric furnace method. Generally, the three-phase electric furnace method is used. In the electric furnace method, charcoal is directly roasted at 800°C to remove moisture and organic matter and then added to the electric furnace intermittently. Molten sulfur is continuously added to the electric furnace to react with the red charcoal at about 1000°C. The generated carbon disulfide is desulfurized and condensed to obtain a crude product, which is then refined. Distillation and condensation to obtain carbon disulfide finished product. The reaction formula is as follows:

3. Commercially available Carbon disulfide is synthesized by heating charcoal and sulfur to 850 to 950°C. As a reagent, it can meet general requirements, but when the required purity is high, the following methods need to be used to remove the impurities contained in it. These impurities are hydrogen sulfide, sulfurous acid, sulfuric acid, organic sulfides, water and sulfur. Add 100 to 200 g of mercury and an appropriate amount of phosphorus pentoxide to 500 mL of commercially available carbon disulfide, shake for about 1 hour, filter, fractionate the filtrate away from light, discard the high and low fractions, and collect the middle fraction. The collected fractions are remixed with mercury and phosphorus pentoxide, shaken, and fractionated. Repeat this operation until the content of harmful impurities reaches the standard.

Refining method: Impurities contained include sulfur, sulfide and water. There are several refining methods: ① Distill 3 times with a glass still. ② Dry with calcium chloride and then fractionate multiple times. ③ Shake with mercury to remove sulfide, then dry and fractionate with phosphorus pentoxide. ④ Add 5g of crushed potassium permanganate to 1L of carbon disulfide and shake it thoroughly until the hydrogen sulfide is completely removed and then place it. After separation, add a small amount of mercury and shake it to remove the sulfur until the interface does not turn black further. Finally, add 5g of mercury sulfate to each 1L of carbon disulfide and shake to eliminate the odor. After separation, it is dried with calcium chloride and fractionated.

4. Use industrial carbon disulfide as raw material, add anhydrous copper sulfate (25-37.5g copper sulfate is required for each carbon disulfide), stir thoroughly until the black powder disappears and there is no unpleasant smell, immediately Filter to remove insoluble impurities, then add anhydrous copper sulfate to the filtrate, distill, and collect the fractions according to product specifications, which is the pure product.

Purpose

1. Used in the manufacture of viscose fiber, cellophane, xanthate, thiocyanate and carbon tetrachloride. Xanthate produced from carbon disulfide is used as an ore flotation agent in the metallurgical industry. Used in the production of agricultural pesticides. When vulcanized in the rubber industry, it can be used as a solvent for sulfur chloride. Use it to make anti-corrosion agents for equipment and pipelines in ammonia treatment systems. It is also a solvent used for testing primary amines, secondary amines and α-amino acids, measuring refractive index, and chromatographic analysis. It is also used to extract oil from linseed, olive fruit, animal bones, leather and wool. Used as an accelerator in aviation. It is also used as a solvent for grease, wax, paint, camphor, resin, rubber, sulfur, phosphorus, iodine, etc., as a degreaser for wool, as an agricultural pesticide, as a soil disinfectant, as a stain remover for clothes, etc. In analysis, it is used for the determination of primary amines, secondary amines and α-amino acids and as a solvent for infrared spectroscopy.

2. Carbon disulfide is widely used in metallurgy, pesticides, rubber, viscose fiber and other industrial fields. It has good penetrability and is generally used as a mixture with non-combustible ingredients when fumigating grain. Fumigation of dry seeds with carbon disulfide does not reduce seed viability. For grains such as wheat, barley, corn, rice, etc., fumigation at 250g/m3 for 24 hours will not affect germination. Gaseous carbon disulfide will seriously damage or kill growing plants or seedlings. Water-diluted carbon disulfide emulsion treats the soil around the roots of evergreen trees and deciduous seedlings, and can effectively control a variety of underground pests. Due to the flammable and explosive properties of carbon disulfide, this agent is used less and less in modern fumigations.

3. Mainly used as raw material for manufacturing viscose fiber and cellophane. Xanthate produced from carbon disulfide is used as an ore flotation agent in the metallurgical industry. Used in the production of agricultural pesticides. When vulcanized in the rubber industry, it can be used as a solvent for sulfur chloride. It is also a solvent used for testing primary amines, secondary amines and α-amino acids, measuring refractive index, and chromatographic analysis. It is also used to extract oil from linseed, olive fruit, animal bones, leather and wool. Used as aerospace accelerator.

4. Used as analytical reagents, solvents, viscose fibersVJ wool degreaser. Also used for refractive index determination.

5. Used in the manufacture of rayon, pesticides, accelerator M, accelerator D, and also used as solvents. [30]

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5-Chloro-2,4-dimethoxyaniline

5-chloro-2,4-dimethoxyaniline structural formula

Structural formula

Business number 02C7
Molecular formula C8H10ClNO2
Molecular weight 187.62
label

2,4-Dimethoxy-5-chloroaniline

Numbering system

CAS number:97-50-7

MDL number:MFCD00025752

EINECS number:202-586-5

RTECS number:None

BRN number:2211013

PubChem number:24862121

Physical property data

  1. Characteristics: white to light gray crystal.
  2. Density (g/mL, 20℃): Undetermined
  3. Relative vapor density (g/mL, air=1): Undetermined
  4. Melting point ( ºC): 89-92
  5. Boiling point (ºC, normal pressure): Undetermined
  6. Boiling point (ºC, KPa): Undetermined
  7. Refractive index: Undetermined Determined
  8. Flash point (ºC): Not determined
  9. Specific optical rotation (º): Not determined
  10. Autoignition point or ignition temperature (ºC): Not determined Determined
  11. Vapor pressure (mmHg, 20.2ºC): Undetermined
  12. Saturation vapor pressure (kPa, ºC): Undetermined
  13. Heat of combustion (KJ/mol ): Undetermined
  14. Critical temperature (ºC): Undetermined
  15. Critical pressure (KPa): Undetermined
  16. Oil-water (octanol/water) partition coefficient Log value: Undetermined
  17. Upper explosion limit (%, V/V): Undetermined
  18. Lower explosion limit (%, V/V): Undetermined
  19. Solubility: Not determined

Toxicological data

None

Ecological data

None

Molecular structure data

1. Molar refractive index: 45.64

2. Molar volume (cm3/mol): 132.6

3. Isotonic specific volume (90.2K ): 359.2

4. Surface tension (dyne/cm): 53.7

5. Polarizability (10-24cm3): 18.09

Compute chemical data

1. Reference value for hydrophobic parameter calculation (XlogP): 1.8

2. Number of hydrogen bond donors: 1

3. Number of hydrogen bond acceptors: 3

4. Number of rotatable chemical bonds: 2

5. Number of tautomers: none

6. Topological molecule polar surface area 44.5

7. Number of heavy atoms: 12

8. Surface charge: 0

9. Complexity: 145

10. Number of isotope atoms: 0

11. Determine the number of atomic stereocenters: 0

12. Uncertain number of atomic stereocenters: 0

13. Determine the number of chemical bond stereocenters: 0

14. Number of uncertain chemical bond stereocenters: 0

15. Number of covalent bond units: 1

Properties and stability

None

Storage method

None

Synthesis method

None

Purpose

Used in the synthesis of naphthol AS-ITR, Pigment Red 5 and other dyes and their intermediates.

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DL-glyceraldehyde

DL-glyceraldehyde structural formula

Structural formula

Business number 017X
Molecular formula C3H6O3
Molecular weight 90.08
label

None

Numbering system

CAS number:56-82-6

MDL number:MFCD00064379

EINECS number:200-290-0

RTECS number:MA6475000

BRN number:635685

PubChem number:24895192

Physical property data

1. Properties: white crystal.

2. Density (g/mL, 25/4℃): 1.445

3. Relative vapor density (g/mL, air=1): Undetermined

4. Melting point (ºC): 145

5. Boiling point (ºC, normal pressure): Undetermined

6. Boiling point (ºC, 5.2kPa): Undetermined

7. Refractive index: Undetermined

8. Flash point (ºC): Undetermined

9. Specific rotation (º): Undetermined

7. p>

10. Autoignition point or ignition temperature (ºC): Undetermined

11. Vapor pressure (kPa, 25ºC): Undetermined

12. Saturated vapor pressure (kPa, 60ºC): Undetermined

13. Heat of combustion (KJ/mol): Undetermined

14. Critical temperature (ºC): Undetermined

15. Critical pressure (KPa): Undetermined

16. Log value of oil-water (octanol/water) partition coefficient: Undetermined

17. Explosion upper limit (%, V /V): Undetermined

18. Lower explosion limit (%, V/V): Undetermined

19. Solubility: Slightly soluble in water, insoluble in benzene and petroleum ether and pentane.

Toxicological data

1. Acute toxicity: rat abdominal LD50: 2mg/kg 2. Mutagenicity: mutation microorganismsTEST system: bacteria – Salmonella typhimurium: 100ug/plate

Ecological data

None

Molecular structure data

5. Molecular property data:

1. Molar refractive index: 19.16

2. Molar volume (cm3/mol): 70.7

3. Isotonic specific volume (90.2K): 191.2

4. Surface tension (dyne/cm): 53.3

5. Polarizability (10-24cm3): 7.59

Compute chemical data

1. Reference value for calculation of hydrophobic parameters (XlogP): -1.6

2. Number of hydrogen bond donors: 2

3. Number of hydrogen bond acceptors: 3

p>

4. Number of rotatable chemical bonds: 2

5. Number of tautomers: 3

6. Topological molecule polar surface area 57.5

7. Number of heavy atoms: 6

8. Surface charge: 0

9. Complexity: 43.3

10. Number of isotope atoms: 0

11. Determine the number of atomic stereocenters: 0

12. Uncertain number of atomic stereocenters: 1

13. Determine ��Number of stereocenters of chemical bonds: 0

14. Number of stereocenters of uncertain chemical bonds: 0

15. Number of covalent bond units: 1

Properties and stability

None

Storage method

This product should be stored in a sealed, cool place and away from light.

Synthesis method

1. Mix 50g (0.3mol) diethanol acetal DL-glyceraldehyde and 500ml 0.1mol/L sulfuric acid, and place at 20°C for 7 days. After adding 30ml of glacial acetic acid, neutralize with barium hydroxide solution, add 5g of activated carbon, stir and filter. The water in the filtrate was evaporated under reduced pressure, and an equal volume of absolute ethanol was added to the residue. The crystals were filtered out and dried to obtain 22g DL-glyceraldehyde, with a yield of 80%.

2. Preparation method:

Dietol-β-chloroacetaldehyde (3): In a 3L reaction bottle equipped with a stirrer and ventilation tube, add 253 mL of absolute ethanol, cool it to below 0°C in an ice-salt bath, and dry it of hydrogen chloride gas to saturation. While stirring, 112g (2.0 mol) of acrolein (2) cooled to 0°C was added dropwise, the reaction temperature was controlled to 0°C, and the addition was completed in about 1.5 hours. Let stand and separate the layers, separate the lower organic layer, add solid sodium bicarbonate powder in batches, neutralize and remove acid. Filter, wash the filtrate with ice water, and dry over anhydrous potassium carbonate for 10 hours. After filtration, distill under reduced pressure and collect the fractions at 58-62°C/1.06kPa to obtain 112g of diethanol-β-chloroacetaldehyde (3) with a yield of 34%. Diethanol acrolein (4): Add 340g (6mol) of dry powdered potassium hydroxide and 167g (1.0mol) of the above compound (3) into a distillation bottle. After shaking vigorously, install a fractionation device. Heat the distillation bottle in an oil bath at 210 to 220°C until no more distillate is distilled. The water in the distillate was separated, and the organic layer was dried with potassium carbonate, filtered and distilled. The fractions at 122-126°C were collected to obtain 98g of diethanol acrolein (4), with a yield of 75%. Diethylglyceraldehyde (5): In a reaction bottle equipped with a stirrer, thermometer, and dropping funnel, add 65g (0.5mol) of diethylglyceraldehyde (4) and 600mL of water, cool to 5°C, and stir Add dropwise a solution of 80g (0.5mol) water, control the dropping speed to about 25mL/min, and keep the temperature of the reaction solution at about 5°C. Stirring – stop, the reactants will become gel-like. After leaving it for 2 hours, heat it in a steam bath for 1 hour. Filter with suction, and wash the manganese dioxide with 150 mL of water. Combine the filtrate and washing liquid, and add 1200g anhydrous potassium carbonate while cooling. The organic layer was separated, and the aqueous layer was extracted 4 times with diethyl ether. The organic layers were combined and dried over anhydrous potassium carbonate. After recovering the diethyl ether, distill under reduced pressure and collect the fraction at 120-121°C/1.06kPa to obtain 55g of diethyl glyceraldehyde (5) with a yield of 67%. DL-Glyceraldehyde (1): Place 50g (0.3mol) of the above-mentioned diethanol glyceraldehyde (5) and 0.05mol/L sulfuric acid in a reaction bottle, and place it at 20°C for 1 week. Add 30 mL of glacial acetic acid. The reaction compound was carefully neutralized with barium hydroxide solution and decolorized with activated carbon. Filter, and the filtrate is concentrated at a pressure of 1.33kPa. Add an equal volume of absolute ethanol to the remainder and slowly crystallize. Filter the precipitated crystals and vacuum dry them in a vacuum dryer containing soda lime and calcium chloride desiccant to obtain 22g of DL-glyceraldehyde (1) with a yield of 80%. [1]

Purpose

Used in biochemical research, organic synthesis intermediates, and nutritional agents.

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