May 2024 – Page 7 – Pu catalyst

Eugenol

Structural formula

Business number	02CA
Molecular formula	C10H12O2
Molecular weight	164.2
label	eugenol, 4-allyl-2-methoxyphenol, 1-Hydroxy-2-methoxy-4-allylbenzene, 4-allylguaiacol, 4-Allyl-2-methoxyphenol, artificial flavors

Numbering system

CAS number:97-53-0

MDL number:MFCD00008654

EINECS number:202-589-1

RTECS number:SJ4375000

BRN number:1366759

PubChem number:24862128

Physical property data

1. Properties: Colorless or light yellow liquid, the color deepens when exposed to the air or under strong light. There is a strong clove aroma.

2. Melting point (ºC): -9.2~-9.1

3. Boiling point (ºC): 253.2

4. Relative density (20℃, 4 ℃): 1.0672

5. Relative density (25℃, 4℃): 1.0652²⁰

6. Refractive index at room temperature (n²⁰): 1.5405

7. Refractive index at room temperature (n²⁵): 1.5345³⁰

8. Dissolution Properties: Slightly soluble in water, soluble in ethanol, acetone, ethyl acetate, ether, chloroform and other organic solvents.

9.Flash point (℃): >110

Toxicological data

Toxicity classification Poisoning

Acute toxicity: Oral – Rat LD50: 1930 mg/kg; Oral – Mouse LC50: 3000 mg/kg.

Irritation Data: Skin – Rabbit 100 mg/24 hours Severe.

Ecological data

This substance is slightly hazardous to water.

Molecular structure data

1. Molar refractive index: 48.72

2. Molar volume (cm³/mol): 156.2

3. Isotonic specific volume (90.2K ): 384.3

4. Surface tension (dyne/cm): 36.5

5. Dielectric constant:

6. Dipole moment (10^-24cm³):

7. Polarizability: 19.31

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: 2

4. Number of rotatable chemical bonds: 3

5. Number of tautomers: 3

6. Topological molecule polar surface area 29.5

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

1. Avoid contact with oxides.

2. Colorless to light yellow liquid. Rich caramel sweet aroma. The color turns brown and black after being stored for a long time and exposed to air.

3. Exist in oriental tobacco leaves and smoke.

4. Found in clove oil, cinnamon leaf oil, cinnamon bark oil, camphor oil, nutmeg oil, etc.

Storage method

Brown glass bottle with light-sealed packaging. Store in a cool and dark place.

Synthesis method

1. Eugenol mainly exists in clove basil oil and camphor cinnamon leaf oil. It is a component of various aromatic oils, especially clove oil, cinnamon leaf oil, basil oil, and laurel oil. Although eugenol can also be prepared by synthetic methods, it is generally isolated and extracted from plants or aromatic oils in industry.

Take the clove basil and remove the fine roots and Foreign matter, dried and chopped, steam distilled. When distilling, maintain a strong fire and return the distillate to the pot to increase the oil yield. When the final steamed oil-water mixture is around 45°C, the relative density of the essential oil is close to water, and the distillate is white and turbid; when the temperature is between 30 and 40°C, part of the oil floats on the water (the relative density of ocimene is about 0.9) , the other part of the oil sinks underwater (the relative density of eugenol is greater than that of water).

Add 20% sodium hydroxide to the oil-water mixture, and then perform steam distillation to remove all non-acidic substances to obtain a eugenol sodium salt solution. Then add 30% sulfuric acid to neutralize it to pH=2~3 (water layer) with stirring at 50°C, let it stand and separate into layers, take off the crude eugenol oil in the lower layer and conduct distillation under reduced pressure to obtain eugenol.

It is produced by the reaction of o-methoxyphenol and allyl bromide, followed by heating and rearrangement.

2.Isolation method: Add excess sodium hydroxide aqueous solution to the natural essential oil containing eugenol, stir thoroughly, and This generates sodium eugenol that is soluble in water. After the oil layer is separated, the alkaline aqueous solution containing sodium eugenol is acidified with dilute sulfuric acid, and the eugenol is re-precipitated. Separate the eugenol oil layer, wash and dry it, and then distill it under reduced pressure to obtain refined eugenol.

3.The synthesis method uses o-methoxyphenol and allyl chloride as raw materials, in the presence of metallic copper, Heating to about 100℃, eugenol can be generated in one step. Since the boiling points of the three isomers are very close, the separation and purification work is very complicated. Therefore, the isolation method to generate eugenol is still the main method at present.

4. Tobacco: OR, 26; can be separated from clove oil. When the synthetic method uses guaiacol as raw material to prepare eugenol, there are many side reactions, and it is difficult to separate and purify.

Purpose

1. In addition to being used in medicine, it can also be used as a raw material for synthetic fragrances. It can also be used to prepare carnation-flavored daily flavors and can also be used as edible spices.

2.Mainly used for preparing mint, nuts, spicy foods and tobacco flavors. The dosage used in meat is 40~2000mg/kg; in gum, 500mg /kg; in condiments, 9.6~100mg/kg; in baked goods, 33mg/kg; 32 in candiesmg/kg; 3.1 in cold drinks mg/kg; 1.4mg/kg in soft drinks; 0.6 in puddings. In addition, eugenol has antiseptic and strong bactericidal properties and is found naturally in many essential oils.

3.Eugenol is the main fragrance agent for preparing clove, carnation, carnation and other flavors. It is used for preparing woody and oriental flavors. Fixatives and modifiers for fragrances. It is also often used in mint, nuts, spicy food flavors and tobacco flavors, and is also an important raw material for the synthesis of vanillin. It is also used in medicine and oral hygiene products. Eugenol is a commonly used analgesic drug in dentistry. It mainly anesthetizes dental nerves, slows down stimulation and plays an analgesic effect.

4. It is used in the blending of cosmetics, soaps, food and other flavors. Used in the ink industry as an anti-drying agent.

5. Also used as insecticide and preservative.

rodentin

Structural formula

Business number	01TJ
Molecular formula	C14H14O3
Molecular weight	230.26
label	2-Pivaloyl-1,3-indandione, The rat is over, rodentin, pintone, 2-(2,2-Dimethyl-1-oxopropyl)-1H-indene-1,3-(2H)dione, Pival, Pivalyl, Pivacin, ,Pivaldion, Pivalyn, 2-(2,2-Dimethyl-1-oxopropyl)-1H-indene-1,3-(2H)dione, Rodenticide

Numbering system

CAS number:83-26-1

MDL number:MFCD00021230

EINECS number:201-462-8

RTECS number:NK6300000

BRN number:2051258

PubChem number:24899309

Physical property data

1. Character: bright yellow crystal

2. Density (g/mL, 25/4℃): Uncertain

3. &nb

Toxicological data

None

Ecological data

None

Molecular structure data

1. Molar refractive index: 61.75

2. Molar volume (cm³/mol): 192.3

3. Isotonic specific volume (90.2K ): 502.6

4. Surface tension (dyne/cm): 46.6

5. Polarizability (10^-24cm³): 24.48

Compute chemical data

1. Reference value for hydrophobic parameter calculation (XlogP): 2.7

2. Number of hydrogen bond donors: 0

3. Number of hydrogen bond acceptors: 3

4. Number of rotatable chemical bonds: 2

5. Number of tautomers: 3

6. Topological molecule polar surface area 51.2

7. Number of heavy atoms: 17

8. Surface charge: 0

9. Complexity: 351

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

Methyl sulfide

Structural formula

Business number	01J5
Molecular formula	C2H6S
Molecular weight	62.13
label	dimethyl sulfide, dimethyl sulfide, DMS, Dimethyl sulfide, 2-Thiapropane, Methyl sulphide, City gas smell tester, industrial purifier, paint release agent, Battery low temperature preservative, pesticide penetrant

Numbering system

CAS number:75-18-3

MDL number:MFCD00008562

EINECS number:200-846-2

RTECS number:PV5075000

BRN number:1696847

PubChem number:24856582

Physical property data

1. Properties: colorless liquid with unpleasant odor. ^[1]

2. Melting point (℃): -98.3^[2]

3. Boiling point (℃): 37.3^[3]

4. Relative density (water = 1): 0.85^[4]

5. Relative vapor Density (air=1): 2.14^[5]

6. Saturated vapor pressure (kPa): 53.2 (20℃)^[6]

7. Heat of combustion (kJ/mol): -1907.7^[7]

8. Critical temperature (℃): 229^[8]

9. Critical pressure (MPa): 5.69^[9]

10. Octanol/water partition coefficient: 0.92^[10]

11. Flash point (℃): <-17.7^[11]

12. Ignition temperature (℃) ：206^[12]

13. Explosion upper limit (%): 19.7^[13]

14. Explosion lower limit (%) %): 2.2^[14]

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

16. Viscosity (mPa·s, 20ºC): 0.289

17. Viscosity (mPa·s, 25ºC): 0.279

18. Ignition point (ºC): 206.1

19. Heat of evaporation (KJ/mol, 25ºC): 27.61

20. Heat of evaporation (KJ/mol, b.p. ): 27.0174

21. Heat of fusion (KJ/mol): 7.990

22. Heat of formation (KJ/mol, 25ºC): -65.48

23 .Specific heat capacity (KJ/(kg·K), 25ºC, constant pressure): 1.17

24. Boiling point rising constant: 1.85

Toxicological data

1. Acute toxicity:

Rat caliber LD50: 3300mg/kg; rat inhalation LCLO: 40250ppm;

Mouse caliber LD50: 3700mg/kg; mouse inhalation LCLO: 31620 ug/m3;

Mouse abdominal cavity LD50: 8mg/kg; Rabbit skin LD50: >5mg/kg;

Mammal LD50: 1950mg/kg;

2. Other multiple dose toxicity data:

Rat caliber TDLO: 21mg/kg/70D-I; Rabbit caliber TDLO: 24500mg/kg/14W-I;

3. Acute toxicity^[16]

LD50: 535mg/kg (rat oral)

LC50: 102235mg /m³(rat inhalation)

4. Irritation^[17]

Rabbit transdermal: 500mg (24h),Mild irritation.

Rabbit eye: 259μg (24h), severe irritation.

Ecological data

1. Ecotoxicity^[18] LC50: 7.5~15ppm (fish)

2. Biodegradability No data yet

3. Non-biodegradability^[19] In the air, when the hydroxyl radical concentration is 5.00×10^{At 5}pcs/cm³, the degradation half-life is 3.5d (theoretical).

The half-life of photooxidation is 8 hours.

Molecular structure data

1. Molar refractive index: 19.31

2. Molar volume (cm³/mol): 75.5

3. Isotonic specific volume (90.2K ): 162.3

4. Surface tension (dyne/cm): 21.3

5. Polarizability (10^-24cm³): 7.65

Compute chemical data

1. Reference value for hydrophobic parameter calculation (XlogP): 0.9

2. Number of hydrogen bond donors: 0

3. Number of hydrogen bond acceptors: 1

4. Number of rotatable chemical bonds: 0

5. Number of tautomers: none

6. Topological molecule polar surface area 25.3

7. Number of heavy atoms: 3

8. Surface charge: 0

9. Complexity: 2.8

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: 1

Properties and stability

1. Chemical properties: It can form addition compounds with halogens, metal halides, etc. Or react with alkyl halides to form sulfonium compounds. When oxidized, sulfoxide is generated, and continued oxidation generates sulfone. It is easy to burn and explode when exposed to open flames or high heat. Thermal decomposition produces toxic sulfide fumes.

2. This product is poisonous. Low-concentration dimethyl sulfide vapor generally causes nausea and loss of appetite, while high-concentration vapor has a paralyzing effect on the central nervous system. During the production process, it must be sealed to prevent running, popping, dripping and leaking. Ventilation should be strengthened at the production site, and operators should wear protective equipment. In the event of poisoning, you should move to a place with fresh air and seek medical treatment.

3. Stability^[20] Stable

4. Incompatible substances^[21] Strong oxidants, alkalis, ammonia

5. Conditions to avoid contact ^[22] Heat

6. Polymerization hazard^[23] No polymerization

7. Decomposition products^[24] Sulfide

Storage method

Storage Precautions^[25]Stored in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature should not exceed 29°C. The packaging must be sealed and must not come into contact with air. They should be stored separately from oxidants, alkalis, and ammonia, 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 emergency release equipment and suitable containment materials.

Synthesis method

1. Refining method: Use the complex formed between mercuric chloride and methyl sulfide for refining: add 1 mol of mercuric chloride to 1250 mL of ethanol, and then add 0.67 mol of methyl sulfide alcohol solution to this solution. The resulting solid is recrystallized to obtain complex crystals with a certain melting point and a structure of 2(CH3)2S·HgCl2. Dissolve 250 mL of concentrated hydrochloric acid in 780 mL of water, add 500 g of the refined complex, and heat to separate the methyl sulfide. After washing with water and drying with calcium chloride, the purity can reach 99.995% (mol).

Purpose

1. This product is a solvent and an intermediate for the production of dimethyl sulfoxide, methionine and pesticides. It can be used as a solvent for organic compounds, resins, inorganic compounds, polymerization reactions and cyanide reactions. Used as analytical reagent, polyacrylonitrile and other synthetic fiber spinning and hydraulic oil. It can also be used as an odorant for city gas, an industrial purifier, a paint release agent, a low-temperature preservative for batteries, a pesticide penetrant, etc. Used topically in hematological medicines, phytopathology and nutrition.

2. Used as solvent and catalyst for most inorganic substances. ^[26]

L-glutamic acid

Structural formula

Business number	0180
Molecular formula	C5H9NO4
Molecular weight	147.13
label	(S)-2-Aminoglutaric acid, glutamine, (S)-2-Aminoglutaric acid, L-Glutamic acid, (S)-(+)-Glutamic acid, Bitter remover, intermediates, Biochemical reagents

Numbering system

CAS number:56-86-0

MDL number:MFCD00002634

EINECS number:200-293-7

RTECS number:LZ9700000

BRN number:1723801

PubChem number:24901609

Physical property data

1. Characteristics: L-glutamic acid is white or colorless scaly crystals, slightly acidic. The racemate, DL-glutamic acid, is a colorless crystal.

2. Density (g/mL, 25/4℃): Racemic: 1.4601; Dextral, left-handed: 1.538.

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

4. Melting point (ºC): 160

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): [α]D22.4+31.4° (C=1.6mol/L hydrochloric acid)

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) distribution coefficient: Undetermined

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

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

19. Solubility: racemateSlightly soluble in cold water, easily soluble in hot water, almost insoluble in ether, ethanol and acetone. The racemate is slightly soluble in ethanol, ether and petroleum ether.

Toxicological data

1. Acute toxicity: human oral TDLo: 71mg/kg; human intravenous TDLo: 117mg/kg; rat oral LD50: 36mg/kg; rabbit oral LD50: >2300mg/kg 2. Mutagenicity: sister chromatids exchangeTEST system:�Lymphocytes: 10mg/L

Ecological data

General remarks

Water hazard level 1 (German regulations) (self-assessment via list) This substance is slightly hazardous to water.

Do not allow undiluted or large amounts of product to come into contact with groundwater, waterways or sewage systems.

Do not discharge materials into the surrounding environment without government permission.

Molecular structure data

1. Molar refractive index: 31.83

2. Molar volume (cm³/mol): 104.3

3. Isotonic specific volume (90.2K ): 301.0

4. Surface tension (dyne/cm): 69.2

5. Polarizability (10^-24cm³): 12.62

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: 4

5. Number of tautomers: none

6. Topological molecule polar surface area 101

7. Number of heavy atoms: 10

8. Surface charge: 0

9. Complexity: 145

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. This product is non-toxic.

2.Odorless, with a slightly special and sour taste.

3. Exist in tobacco leaves and smoke.
　

Storage method

1. This product should be sealed and stored in a cool, dark place.

2. Packed in plastic bags, nylon bags or plastic woven bags, net weight 25kg. During storage and transportation, attention should be paid to moisture-proof, sun-proof and low-temperature storage.

Synthesis method

1. Glutamic acid can be produced by protein hydrolysis and synthesis, but fermentation is currently the main method for producing glutamic acid. The carbon source for fermentation to produce glutamic acid is hydrolyzed sugar or molasses from potato, corn, tapioca starch, coconut tree starch and other starches. It can also be acetic acid, liquid paraffin (C16 paraffin is best) and other petrochemical products. The carbon source is Nutrients that constitute the carbon framework and energy in microbial cells and metabolites. Nitrogen sources are ammonium salts, urea, etc. Nitrogen is the main element that constitutes bacterial cell proteins and nucleic acids. Nitrogen is also the main element that constitutes the glutamic acid amino group of fermentation products. Other auxiliary raw materials are inorganic salts, vitamins, etc. For example, microorganisms require appropriate phosphorus concentration, magnesium is an inorganic activator that stimulates bacterial growth, potassium salt promotes acid production, and corn steep liquor provides biotin and organic nitrogen sources. Various accelerators and additives are also included. The producing bacteria are Brevibacterium, Corynebacterium pekinensis, etc. In a large fermentation tank, ferment with aeration and stirring at a temperature of 30-34°C and a pH>7-8. After 30-40 hours of fermentation, remove bacteria and extract glutamic acid from the fermentation liquid. After refining, the finished product is obtained. In the above process Extraction using isoelectric point method, ion exchange method, hydrochloride method, direct concentration method (when acetic acid is used as raw material), etc. can also be used. The product produced by fermentation method is L-glutamic acid, with a content of more than 98%. Each ton of glutamic acid consumes 4000kg of starch (80%) and 25kg of bacteria. The advantage of the synthesis method is that it does not consume food, but the production process requires high pressure (about 20MPa), high temperature (above 120°C), and uses toxic raw materials. The equipment investment is twice as high as that of the fermentation method, and the racemic glutamic acid obtained needs to be further processed. Split, the production process is complex. Calculated based on the production of 1 ton of 99% sodium glutamate (MSG), the synthesis method consumes 640kg of acrylonitrile. When the annual output is more than 5,000t, the production cost is close to that of the acidification method.
2.Fermentation method

3. Chemical synthesis

4.This product is mainly made from fermentation Produced by law. Molasses or starch is used as the raw material, Corynebacterium glutamicum or Pediococcus or Arthrobacter is used as the strain, and urea is used as the nitrogen source. Fermentation is carried out at 30 to 32°C. After the fermentation is completed, the bacteria are separated from the fermentation liquid. Use hydrochloric acid to adjust the pH value to 3.0, perform isoelectric point extraction, and obtain glutamic acid crystals after separation. The glutamic acid in the mother liquor is extracted with 732 ion exchange resin, crystallized, and dried to obtain the finished product.

5. Tobacco: BU, 22; FC, 21; L-isomer can be obtained from animal and plant proteins through hydrolysis, decolorization, concentration, and crystallization. It can also be produced from sugar or starch by fermentation. The racemate can be synthesized from acrylonitrile.

Purpose

1.L-Glutamic acid is mainly used in the production of MSG and spices, as well as as salt substitutes, nutritional supplements and biochemical reagents. L-glutamic acid itself can be used as a drug, participating in the metabolism of protein and sugar in the brain and promoting the oxidation process. It combines with ammonia in the body to form non-toxic glutyl glutamic acid.Amine can reduce blood ammonia and relieve symptoms of hepatic coma. It is mainly used to treat hepatic coma and severe liver insufficiency, but the efficacy is not very satisfactory; combined with anti-epileptic drugs, it can still treat petit mal epilepsy and psychomotor seizures. Racemic glutamate is used in the production of drugs and as biochemical reagents.

2.Usually not used alone, but in conjunction with phenolic and quinone antioxidants to obtain good synergistic effects.

3.Glutamic acid is used as a complexing agent for electroless plating.

N-phenylsuccinimide

Structural formula

Business number	01TH
Molecular formula	C10H9NO2
Molecular weight	175.18
label	N-Phthalosuccinimide, 1-Phenylsuccinimide

Numbering system

CAS number:83-25-0

MDL number:None

EINECS number:None

RTECS number:None

BRN number:None

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):1551

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

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. 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): 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: 46.71

2. Molar volume (m³/mol）：136.9

3. isotonic ratio (90.2K):371.0

4. Surface Tension (dyne/cm):53.8

5. Polarizability（10^-24cm³):18.52

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: 1

5. Number of tautomers: 3

6. Topological molecule polar surface area 37.4

7. Number of heavy atoms: 13

8. Surface charge: 0

9. Complexity: 215

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

L-Glutamine

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.

2-methoxy-4-nitroaniline

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

Appearance: yellow or tan powder
Density (g/mL, 20℃): 1.2112
Relative vapor density (g/mL , air = 1): not determined
Melting point (ºC): 137-140
Boiling point (ºC, normal pressure): not determined
Boiling point (ºC , KPa): not determined
Refractive index: not determined
Flash point (ºC): not determined
Specific rotation (º): not determined
Autoignition point or ignition temperature (ºC): Not determined
Vapor pressure (mmHg, 20.2ºC): Not determined
Saturation vapor pressure (kPa, ºC ): Undetermined
Heat of combustion (KJ/mol): Undetermined
Critical temperature (ºC): Undetermined
Critical pressure (KPa): Undetermined Determined
Log value of oil-water (octanol/water) partition coefficient: Undetermined
Explosion upper limit (%, V/V): Undetermined
Explosion Lower limit (%, V/V): Undetermined
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.

Formaldehyde oxime

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℃)：1． 035

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. Polarizability（10^-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.

L-aspartic acid

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].

2,5-Dimethyl-1-phenylpyrrole

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. Polarizability（10^-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