hypoxanthine

Hypoxanthine structural formula

Structural formula

Business number 01FE
Molecular formula C5H4N4O
Molecular weight 136.11
label

1,7-dihydro-6H-purin-6-one,

6-Hydroxypurine,

6-Hydroxypurine,

6-oxopurine,

Hypoxanthine,

6-hypoxanthine,

Purine-6(1H)-one

Numbering system

CAS number:68-94-0

MDL number:MFCD00005725

EINECS number:200-697-3

RTECS number:UP0791000

BRN number:5811

PubChem number:24895850

Physical property data

1. Character:Needle crystal


2. Density (g/mL,25/4℃): Unsure


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


4. Melting point (ºC):>360


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


6. Boiling point (ºC, 5.2kPa): Unsure


7. Refractive index:Not sure


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 water) partition coefficient: Uncertain


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


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


19. Solubility:Almost insoluble in water0.078/100m1(19℃)1.4g/100ml(100℃) . Soluble in dilute acids and alkalis, such as 0.5mol/LSulfuric acid or10mol /LSodium hydroxide

Toxicological data

Acute toxicity: mouse abdominal D50: 750 mg/kg;
Reproduction: mouse abdominal cavityTDLo：600 mg/kgSEX/DURATION : female 13 day(s) after conception;
Mouse abdominal cavityTDLo：1 gm/kgSEX/DURATION : female 13 day(s) after conception;

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: 2

3. Number of hydrogen bond acceptors: 2

4. Number of rotatable chemical bonds: 0

5. Number of tautomers: 8

6. Topological molecule polar surface area 70.1

7. Number of heavy atoms: 10

8. Surface charge: 0

9. Complexity: 190

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

Together with xanthine, it is widely present in animals and plants. The inosinic acid of its nucleotide is the precursor of the purine nucleotide of nucleic acid. It is also the parent body of caffeine. Hypoxanthine can be produced through the action of adenine deaminase or nitrite.Purine deamination can also result in the phosphorolysis of inosine through nucleoside phosphorylase.

Storage method

This product should be kept sealed, cool and dry.

Synthesis method



Ethyl cyanoacetate, sodium ethoxide, and thiourea The combination reaction gives 2- Thiol-4-Amino -6-Hydroxypyrimidine , and then undergo nitrosation, reduction, elimination, and cyclization to obtain 6-Hydroxypurine.

Purpose

Anti-malignant tumor drugs6-Intermediate of mercaptopurine.

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D-cycloserine

D-cycloserine structural formula

Structural formula

Business number 01FD
Molecular formula C3H6N2O2
Molecular weight 102.09
label

(R)-(+)-cycloserine,

D-4-amino-3-isoxazolidinone,

cycloserine,

D-4-amino-3-isoxazolidinone,

4-Amino-3-isoxazolidinone,

(R)-4-Amino-3-isoxazolidinone,

Cycloserine,

Genetic engineering research reagents

Numbering system

CAS number:68-41-7

MDL number:MFCD00005353

EINECS number:200-688-4

RTECS number:NY2975000

BRN number:80798

PubChem number:24892907

Physical property data

1. Properties: Colorless needle-like or leaf-like crystals or amorphous powder

2. Density (g/mL, 25/4℃): Uncertain

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

4. Melting point (ºC): 155-156 (decomposition)

5. Boiling point (ºC, normal Pressure): Uncertain

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

7. Refractive index: Uncertain

8. Flash point ( ºC): Uncertain

9. Specific optical rotation (º): 111 º (C=5, 2N NaOH)

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

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

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

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

14. Critical temperature (ºC): Uncertain

15. Critical pressure (KPa): Uncertain

16. The logarithmic value of the oil-water (octanol/water) partition coefficient: Uncertain

17. The upper explosion limit (%, V/V): Uncertain

18. The lower explosion limit (%, V/V): Uncertain

19. Solubility: Soluble in water, slightly soluble in methanol, ethanol, butanol, propylene glycol, isopropyl alcohol and acetone, hardly soluble or insoluble in toluene, Chloroform, ether, pyridine, benzene and carbon disulfide

Toxicological data

None

Ecological data

None

Molecular structure data

1. Molar refractive index: 22.47

2. Molar volume (cm3/mol): 79.8

3. Isotonic specific volume (90.2K ): 201.9

4. Surface tension (dyne/cm): 40.8

5. Polarizability (10-24cm3): 8.90

Computing chemical data

1. Hydrophobic parameter calculation reference value (XlogP): -1.5

2. Number of hydrogen bond donors: 2

3. Number of hydrogen bond acceptors: 3

p>

4. Number of rotatable chemical bonds: 0

5. Number of tautomers: 5

6. Topological molecular polar surface area (TPSA): 64.4

7. Number of heavy atoms: 7

8. Surface charge: 0

9. Complexity: 92.9

10. Isotopic atoms Quantity: 0

11. Determine the number of atomic stereocenters: 1

12. Uncertain number of atomic stereocenters: 0

13. Determine the chemical bond establishment Number of 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 sealed and stored in a cool, dry place away from light.

Synthesis method

Cycloserine can be prepared by fermentation or direct synthesis. The bacteria produced by the fermentation method is Actinomyces laven-dulae, and the fermentation medium is dextrin, glucose, starch, soybean cake powder, yeast powder, ammonium sulfate, ammonium nitrate, calcium carbonate, sodium chloride, magnesium sulfate and soybean oil, etc. The synthesis method is to react β-aminooxyalanine ethyl ester dihydrochloride with potassium hydroxide to obtain cycloserine through cyclization.

Purpose

Antibiotic drugs. For infections caused by drug-resistant Mycobacterium tuberculosis.

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β-estradiol

β-estradiol structural formula

Structural formula

Business number 013E
Molecular formula C18H24O2
Molecular weight 272.38
label

Ovocylin,

Dihydroxyestrin,

Estr-1,3,5-(10)-triene-3β,17β-diol,

1,3,5-Estratriene-3,17β-diol,

17β-Estradiol,

3,17β-Dihydroxy-1,3,5(10)-estratriene,

Dihydrofolliculin,

Estradiol; Estradiol; Courtship diol; Dihydroxyestradiol; Estradiol,

Enzymes·Proteins·Peptides

Numbering system

CAS number:50-28-2

MDL number:MFCD00003693

EINECS number:200-023-8

RTECS number:KG2975000

BRN number:1914275

PubChem number:24278426

Physical property data

1. Properties: White or milky white leaf-like or needle-like crystals (ethanol solution); odorless. Stable in air

2. Density (g/mL, 25/4℃): Not determined

3. Relative vapor density (g/mL, air=1): Not determined Determined

4. Melting point (ºC): 178-179 °C (lit.)

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

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

7. Refractive index: 80.4 ° (C=1, Dioxane)

8. Flash point (ºC): Not determined

9. Specific rotation (º): Undetermined

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

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

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

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

14. Critical temperature (ºC): Undetermined

15. Critical pressure (KPa): Undetermined

16. Oil and water (octanol/water) distribution Log value of coefficient: Undetermined

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

18. Explosion lower limit (%, V/V): Undetermined 19. Solubility : Easily soluble in ethanol, soluble in acetone, chloroform, dioxane and alkali solution, slightly soluble in vegetable oil, almost insoluble in water

Toxicological data

Acute toxicity:

Main irritant effects:

On skin: Irritation to skin and mucous membranes

On eyes: Irritating effects.

Sensitization: No known sensitizing effects.

Ecological data

General notes

Water hazard level 3 (Germany�Example) (Self-assessment via list) This substance is extremely hazardous to water.

Do not allow this product to come into contact with groundwater, waterways or sewage systems, even in small amounts.

Even extremely small amounts of product seeping into the ground can pose a hazard to drinking water

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

Molecular structure data

1. Molar refractive index: 79.50

2. Molar volume (cm3/mol): 232.6

3. Isotonic specific volume (90.2K ): 615.4

4. Surface tension (dyne/cm): 48.9

5. Polarizability (10-24cm3): 31.51

Compute chemical data

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

2. Number of hydrogen bond donors: 2

3. Number of hydrogen bond acceptors: 2

4. Number of rotatable chemical bonds: 0

5. Number of tautomers: 9

6. Topological molecule polar surface area 40.5

7. Number of heavy atoms: 20

8. Surface charge: 0

9. Complexity: 382

10. Number of isotope atoms: 0

11. Determine the number of atomic stereocenters: 5

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

The effect of estrogen can promote the development of secondary sexual characteristics and the final formation of sexual organs in underage girls. In adult women, in addition to maintaining the above-mentioned secondary sexual characteristics, it can also cause a series of changes in the endometrium to produce cyclic menstruation. It can also increase the activity of the uterus and fallopian tubes and increase the sensitivity of uterine muscles to oxytocin. In addition, estrogen can also increase the deposition of bone calcium salts and accelerate epiphyseal closure. In large doses, it can increase serum triglycerides and phospholipids, causing water and sodium retention. At larger doses, estrogen can also act on the hypothalamic-pituitary system, inhibit the secretion of gonadotropins and prolactin, and offset the main effects of androgens.

Storage method

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

Synthesis method

1. Use androst-4-en-19-desmethyl-3,17-dione to introduce bromine at the 2- and 6-positions through bromination, and then add bromine to 4-ethyl-2-methylpyridine In the presence of dehydrobromination (elimination), 2,4,6-androstatriene-19-desmethyl-3,17-dione is generated, which is then cracked at high temperature to generate estrone, and then lithium aluminum hydrogen is reduced to produce Get this product.

Purpose

1. Intermediates of estradiol valerate and estradiol benzoate.

2.Estrogen drugs. It is used for functional uterine bleeding, primary amenorrhea, menopausal syndrome and prostate cancer.

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1,4-Bis(trichloromethyl)benzene

1,4-bis(trichloromethyl)benzene structural formula

Structural formula

Business number 01FC
Molecular formula C8H4Cl6
Molecular weight 312.84
label

1,4-Bis(trichloromethyl)benzene,

α,α,α,α’,α’,α’-hexachloro-p-xylene,

For hexachlorobenzyl,

Hexachloroparaxylene,

1,4-bistrichlorotoluene,

Α,Α,Α,Α’,Α’,Α’-hexachloro-p-xylene,

antischistosomiasis drugs

Numbering system

CAS number:68-36-0

MDL number:MFCD00000791

EINECS number:200-686-3

RTECS number:ZE4655000

BRN number:None

PubChem ID:None

Physical property data

1. Properties: White needle-like crystals or crystalline powder, with a special odor and tasteless. It will slowly decompose when exposed to light and alkali and become acidic

2. Density (g/mL, 25/4℃): Uncertain

3. Relative vapor density (g/mL, Air=1): Uncertain

4. Melting point (ºC): 106-110

5. Boiling point (ºC, normal pressure): 312

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

7. Refractive index: Uncertain

8. Flash point (ºC): Uncertain

9 . Specific rotation (º): Uncertain

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

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

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

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

14. Critical temperature (ºC): Uncertain

15. Critical pressure (KPa): Uncertain

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

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

18. Explosion lower limit (%, V/V): Uncertain

19. Solubility : Insoluble in water, easily soluble in ethanol, xylene, petroleum ether and vegetable oil, etc.

Toxicological data

Acute toxicity: Rat oral LD50: 3200 mg/kg; Breeding: Rat oral TDLo: 2330 mg/kgSEX/DURATION: male 26 week(s) pre-mating; Rat oral TDLo: 2330 mg/kgSEX/ DURATION: female 26 weeks(s) pre-mating;

Ecological data

None

Molecular structure data

1. Molar refractive index: 64.32

2. Molar volume (cm3/mol): 192.0

3.   Isotonic volume (90.2K): 495.2

4. Surface tension (dyne/cm): 44.2

5. Polarizability (10-24cm3): 25.50

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: 0

4. Number of rotatable chemical bonds: 0

5. Number of tautomers: none

6. Topological molecule polar surface area 0

7. Number of heavy atoms: 14

8. Surface charge: 0

9. Complexity: 161

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

Store in an airtight container away from light.

Synthesis method

Using mixed xylene as raw material, it is first sulfonated with 98% sulfuric acid to generate m-xylene sulfonate. The oil layer containing o- and p-xylene is separated from the sulfonation reaction product, washed with water, dried, and o- and p-xylene is distilled under reduced pressure. The by-product m-xylene can be obtained by hydrolysis of m-xylene sulfonate. 1,4-bis(trichloromethyl)benzene is obtained by chlorination of o- and p-xylene: put o- and p-xylene into the reaction pot, and then add benzoyl peroxide and triethanolamine. After heating to 70°C, introduce chlorine gas under light irradiation, react at 70-80°C for 6 hours, and then raise the temperature to 100-120°C to continue the reaction until the relative density of the reaction solution reaches 1.560-1.580 (65°C), which is the end point of the reaction. Stop passing chlorine and remove residual chlorine under reduced pressure. Cool to 5°C, filter, wash to obtain crude product, recrystallize, and decolorize with activated carbon to obtain finished product.

Purpose

Anti-schistosomiasis drugs. It has certain effects on liver fluke disease, amoebiasis, malaria and intestinal nematodes. However, adverse reactions to the nervous system are more common, and delayed reactions last longer.

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Catalysts: The Unseen Heroes of Chemical Reactions

Catalysts are substances that increase the rate of a chemical reaction without being consumed in the process. They play a crucial role in various industrial, biological, and environmental processes. This essay will delve into the importance, types, and applications of catalysts, shedding light on these unseen heroes that make countless reactions possible.

Importance of Catalysts

Catalysts are vital for several reasons. Firstly, they significantly speed up chemical reactions, making industrial processes more efficient and cost-effective. Without catalysts, many reactions would occur too slowly or require extremely high temperatures and pressures, making them impractical or uneconomical.

Secondly, catalysts enable selective reactions, allowing the production of specific compounds without unwanted by-products. This selectivity is essential in the synthesis of pharmaceuticals, agrochemicals, and other complex molecules.

Thirdly, catalysts contribute to environmental sustainability. They facilitate cleaner reactions, reducing waste and energy consumption. Moreover, they play a key role in pollution control, such as in catalytic converters that remove harmful emissions from vehicle exhausts.

Types of Catalysts

Catalysts can be broadly classified into two categories: homogeneous and heterogeneous.

Homogeneous catalysts are present in the same phase as the reactants. They often consist of metal ions, acids, or bases dissolved in a liquid solution. Homogeneous catalysts are highly efficient and selective, but their recovery and separation from the products can be challenging.

Heterogeneous catalysts, on the other hand, exist in a different phase than the reactants, typically as solids. They offer the advantage of easy separation and reuse. Common examples include metal surfaces, metal oxides, and zeolites. However, their activity and selectivity can be influenced by various factors, such as surface area, particle size, and temperature.

Applications of Catalysts

Catalysts find extensive applications in numerous industries and natural processes.

In the chemical industry, catalysts are used in the production of basic chemicals like ammonia, sulfuric acid, and polymers. For instance, the Haber-Bosch process, which converts nitrogen and hydrogen into ammonia, relies on an iron-based catalyst.

In the petroleum industry, catalytic cracking and reforming are essential processes for refining crude oil into gasoline, diesel, and other petrochemicals. Catalysts like zeolites and platinum-based compounds break down larger hydrocarbon molecules and rearrange them into more valuable products.

In biology, enzymes act as natural catalysts, accelerating biochemical reactions in living organisms. Enzymes facilitate processes such as digestion, metabolism, and DNA replication with remarkable efficiency and specificity.

In environmental protection, catalysts help mitigate pollution and promote sustainable practices. Catalytic converters in automobiles convert toxic gases like carbon monoxide, nitrogen oxides, and hydrocarbons into less harmful substances. Additionally, catalysts are used in wastewater treatment and green energy technologies, such as fuel cells and solar cells.

 

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DMAPA

Silane modified polyether sealant

Silane modified polyether sealant
1、 Introduction to Silane Modified Polyether Sealant
Silane modified polyether sealant (MS sealant), also known as organosilicon modified polyether sealant and end silyl polyether sealant, is a high-performance environmentally friendly sealant prepared based on end silyl polyether (with polyether as the main chain and siloxane at both ends) as the basic polymer.
Due to its combination of advantages and strengths of silicone sealant and polyurethane sealant, it exhibits excellent weather resistance, durability, high resistance to deformation and displacement, good adhesion, coating, environmental friendliness, low contamination, low viscosity, and excellent workability. It has increasingly attracted attention from the domestic construction industry, and in industrial fields such as automotive manufacturing, rail transit, container manufacturing, equipment manufacturing, etc The fields of electronics and electrical engineering are also being increasingly promoted and applied.
Synthesis of Silane Modified Polyether
The structural feature of silane modified polyether is that the main chain is a macromolecular polyether, and the end group is a silane group containing hydrolyzable groups. The synthesis of silane modified polyethers is usually completed by a two-step method.
Step: Using allyl polyether alcohol, hydroxyl terminated polyether, etc. as raw materials, dihalomethane (H2CX2) as a chain extender, and caustic soda as a catalyst, an allyl terminated polyether intermediate is prepared through chain extension reaction.
Step 2: In the presence of platinum based catalysts, the refined intermediate is reacted with methyldimethoxysilane through terminal silylation reaction to obtain silane modified polyether.
Curing mechanism of silane modified polyether sealant
The curing mechanism of MS sealant belongs to wet curing. Under the presence of room temperature, moisture, and appropriate catalysts (amines, tin, etc.), the alkoxy group in the terminal alkoxy group is first hydrolyzed into a silanol group (Si-OH); Subsequently, Si-O-Si bonds are formed by condensation between Si-OH groups or between Si-OH and Si-OCH, releasing water or methanol; After crosslinking, a flexible polyether chain structured elastomer is formed with Si-O-Si bonds as network crosslinking points.


Advantages of Silane Modified Polyether Sealant
Comparison of performance between silane modified polyether adhesive, silicone sealant, and polyurethane sealant:
The reason why silane modified polyether adhesive has such good comprehensive properties is closely related to the special structure of its base polymer (silyl terminated polyether).
Characteristics of Silane Modified Polyether Sealant
1. Widespread adhesion to substrates. Due to the low surface energy and high permeability of the base polymer (silyl terminated polyether), it has good wetting ability to most inorganic, metal, and plastic substrates, thereby producing good adhesion to the substrate.
2. Excellent weather resistance and durability. End silyl polyethers are composed of polyethers as long chains and terminated with siloxy groups. The long chains of polyethers have the characteristics of low unsaturation, high molecular weight, and narrow distribution. The end groups are hydrolyzable siloxane groups. Silane modified polyether sealant will form a network structure connected by flexible polyether long chains with Si-O-Si bonds as crosslinking points after room temperature moisture curing. This system not only has excellent weather resistance, water resistance, aging resistance, and durability, but also effectively suppresses and avoids the formation of surface cracks of the sealant after long-term use.
3. Environmental friendliness. Silyl terminated polyether is a long-chain structure of polyether terminated with siloxy groups, which does not contain toxic isocyanate groups or free isocyanates like polyurethane sealant. End silyl polyether has low viscosity, good workability, and does not require the use of organic solvents to adjust the process performance of the formula. Therefore, silane modified polyether adhesive can completely achieve no addition of any organic solvents, and its total volatile organic compounds (VOC) are very low.
4. Paintability. Ordinary silicone sealant surfaces cannot be painted or colored, and can only be adjusted to the desired color according to user needs; Silane modified polyether adhesive can be painted and colored, and has good coating properties.
Technical progress of silane modified polyether sealant
In the 1970s, Kaneka Corporation in Japan developed organosilicon modified polymers with polyether frameworks. In 1974, it was the first to develop organosilicon modified polyether sealant. In 1978, it achieved industrial production and was named “Zhong Hua MS Polymer” in 1979. In 1981, it was used at the Tokyo headquarters of Di Ichikangyo Bank in high-rise buildings, marking the market recognition of organosilicon modified polyether sealant.
In recent years, domestic researchers have conducted relevant research on MS sealant. Zhang Huji et al. prepared a single component MS sealant using MS prepolymer, plasticizer, calcium carbonate, gas-phase silica, silane coupling agent, and catalyst as raw materials. Xue Jidong et al. prepared a single component moisture cured MS sealant based on silyl terminated polyether (MS) as the basic polymer. Chen Zhonghua et al. prepared a high-performance single component sealant using Wacker STP-E30 and STP-E35 as base polymers. Huang Huoyang et al. prepared environmentally friendly single component silicone modified polyether sealant using organic silicon modified polyether resin, polypropylene glycol oxide, fillers, silane coupling agents, and catalysts.
At present, domestic Ms adhesive is developing towards multifunctional products. Yang Jing et al. prepared a transparent single component silicone modified polyether sealant, which has excellent weather resistance, high resistance to deformation and displacement, as well as good adhesion, coating, low contamination, and environmental friendliness. The products manufactured by Zhou Rujiang and others have excellent flame retardancy and good adhesion, making them suitable for adhesive sealing in construction, transportation, solar energy, and other fields. Wang Cuihua and others prepared a two-component MS sealant that can quickly cure at low temperatures, and it has good adhesive processability and storage stability.
Application of Silane Modified Polyether Sealant
Silane modified polyether sealant itself has elasticity and can withstand material expansion and vibration, making it difficult to peel off, and can maintain performance for a long time; Due to its superior adhesive performance, it can be used for various purposes; Non polluting stone, with almost no odor or volatile components; Can be used as a post coating and can be sprayed wet to wet; The curing process produces no bubbles and does not affect the mechanical properties of the material. Based on this, sealant can be applied in the following fields:
1. In the field of architecture: leak prevention and sealing of building roofs, sealing of air conditioning systems, repairing cracks in buildings, installation of skylights and flooring, composite decorative panels, sealing of joints in ancillary facilities such as kitchens and bathrooms, sealing of residential doors and windows with concrete structures.
2. Industrial field: Sealing of doors, windows, and windshields for automobiles and high-speed trains, bonding of ceiling floors and frame frames, bonding and sealing of ships, containers, food refrigerated trucks, etc., and bonding and sealing of reinforcement ribs for elevator cars.
3. Product assembly field: Bonding of the same or different materials, assembly of laminated board bonding seals and decorative panels, and assembly of mechanical components.
epilogue
The technology of silane modified polyether sealant abroad has become relatively mature. In Japan and Europe and America, the market share of silane modified polyether sealant has reached over 30%, with a clear upward trend in recent years. However, China is relatively weak in aspects such as prepolymer synthesis, sealant preparation, and engineering application technology research. Due to the monopoly of prepolymer synthesis technology by foreign countries, the procurement price of silane modified polyether sealant is high, It is still difficult for large-scale industrial production and application in China.
With the rapid development of China’s economy and the continuous improvement of people’s living standards, the demand for sealant is bound to move towards high-end development. Therefore, in-depth research on the synthesis mechanism of silane modified polyether prepolymers, solving the process control problems of large-scale production, forming silane modified polyether prepolymer synthesis technology with independent intellectual property rights, and increasing the research and development, production, and engineering application of silane modified polyethers play a crucial role in industries such as aviation, construction, bridges, and trains in China that require high-performance sealing products.
MS adhesive catalyst catalog
NT CAT MS220 is an environmentally friendly metal composite catalyst that does not contain RoHS restricted polybrominated biphenyls, polybrominated diphenyl ethers, lead, mercury, cadmium, and nine types of organic tin compounds such as octyltin, butyl tin, and phenyl tin. It can be used in polyurethane leather, coatings, adhesives, and silicone rubber, especially suitable for MS adhesives.
NT CAT E-14 is widely used in polyurethane foam, elastomer, adhesive, MS sealant and room temperature curing silicone system;
NT CAT E-15 is suitable for aromatic isocyanate two-component polyurethane adhesive system, with moderate catalytic activity and lower activity than A-14;
NT CAT E-16 is suitable for aromatic isocyanate two-component polyurethane adhesive systems, with a delay effect and certain water resistance, and a long storage time for composite materials;
NT CAT E-128 is suitable for polyurethane two-component rapid curing adhesive systems, with strong catalytic activity in this series of catalysts, especially suitable for aliphatic isocyanate systems;
NT CAT E-129 is suitable for aromatic isocyanate two-component polyurethane adhesive system, with strong delay effect and strong stability with water;
NT CAT E-138 is suitable for aromatic isocyanate two-component polyurethane adhesive system, with moderate catalytic activity, good fluidity and hydrolysis resistance;
NT CAT E-154 is suitable for the two-component polyurethane adhesive system of aliphatic isocyanates and has a delay effect;
NT CAT E-159 is suitable for aromatic isocyanate two-component polyurethane adhesive system and can be used to replace A-14, with an addition amount of 50-60% of A-14;
NT CAT MB20 gel catalyst can be used to replace tin metal catalyst in soft bulk foam, high-density soft foam, spray foam, microporous foam and hard foam system, and its activity is relatively lower than that of organic tin;
NT CAT T-12 dibutyltin dilaurate, gel type catalyst, suitable for polyether type high-density structural foam, polyurethane coating, elastomer, adhesive, room temperature curing silicone rubber, etc;
NT CAT T-125 organotin strong gel catalyst, compared with other dibutyltin catalysts, T-125 catalyst has higher catalytic activity and selectivity for carbamate reaction, and improves hydrolysis stability, which is suitable for rigid polyurethane spray foam, molded foam and CASE applications.

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Organic tin manufacturers

Organotin is a kind of organotin compound, which is mainly used in PVC liquid stabilizer, acrylate additives and other fields. Suzhou Haoruicheng Chemical New Material Co., Ltd. and Shanghai Shule Industry (Shanghai) Co., Ltd. are both manufacturers of organotin. Organotin is a chemical widely used in chemical, plastic and other fields. The following are some common organotin manufacturers:

1. Hubei Haopei Chemical Co., Ltd. (Yushui Industrial Park, Jianli County, Jingzhou City, Hubei Province): specializes in the production and sales of organotin stabilizers, organotin catalysts and other products.

2. Fuzhou Aoxing Chemical Co., Ltd. No. 106, Meifeng Road, Shanshan District): mainly produces organotin stabilizers, organotin catalysts, organotin reagents and other products, among which T-181, T-282 and other products are widely used.

3. Jiangsu Jinbo Chemical Co., Ltd. (Wangjiangjing, Haian County, Nantong City, Jiangsu Province Industrial Park): Has rich experience in the production of organotin products, producing organotin catalysts, organotin heat stabilizers, organotin reagents, etc.

4. Beijing Wansheng Trust Chemical Co., Ltd. (Fengtai District, Beijing Kaiyangli Building No. 7): Production of organotin-related products such as organotin stabilizers, organotin catalysts, organotin reagents, etc.

The above companies are just examples, there are many other organic tin manufacturers in the market available. When purchasing organic tin products, you need to pay attention to product quality and safety issues. It is very important to choose reputable manufacturers and qualified products.

Organotin fungicide

Organotin fungicides refer to organic synthetic fungicides containing tin in their chemical structure. Organotin fungicides are mainly used in agriculture, animal husbandry, aquaculture and other fields, such as tributyltin chloride, triphenyltin chloride, etc. Organotin fungicides refer to pesticides containing organotin components. At present, there are mainly the following types:

1. Trimethyltin acetate: also known as TMTD, is a broad-spectrum fungicide that can be used to control a variety of crop diseases, including vegetables, fruits, grains, and trees. It has been used in many countries use is prohibited.

2. Ethylenetrimethylsilyltin (TBTO): It is a broad-spectrum fungicide and algicide, which can be used to protect wood, paper, metal, etc., and can also be used to prevent and control various crop diseases, such as orange blight and grape disease.

3. Cyclohexyltrimethyltin (TCH): commonly used to protect Crops such as fruits and vegetables have a broad-spectrum bactericidal effect.

These organic tin fungicides can effectively control diseases, but they also have certain Toxicity, and may cause pollution to the environment during use. Therefore, it is necessary to abide by relevant safety regulations and operating procedures before use, enhance environmental awareness, and reduce possible safety risks. At the same time, in order to protect the environment and human health, environmentally friendly pesticides and green agricultural production methods should also be promoted.

The Role of Catalysts: Accelerating Change in Chemistry and Beyond

Catalysts play a crucial role in various domains, from chemistry to social change, by accelerating reactions and transformations. This essay explores the role of catalysts, primarily focusing on their function in chemical reactions and their metaphorical application in other fields.

 

Catalysts in Chemistry: The Scientific Perspective
In chemistry, a catalyst is a substance that increases the rate of a chemical reaction without being consumed in the process. Catalysts work by lowering the activation energy required for a reaction to occur, thereby speeding up the reaction rate. They achieve this by providing an alternative pathway for the reaction, which involves lower energy barriers.

 

The role of catalysts in chemical reactions is vital. They enable reactions that would otherwise be too slow or require too much energy to occur under normal conditions. For instance, catalytic converters in cars use catalysts to convert harmful pollutants into less harmful substances, significantly reducing the vehicle’s environmental impact.

Catalysts in Biology: The Life-Sustaining Role
In biology, enzymes act as catalysts, speeding up biochemical reactions that are essential for life. Like chemical catalysts, enzymes lower the activation energy of reactions, allowing them to occur at body temperature and under normal cellular conditions. Without enzymes, many of these reactions would be too slow to sustain life.

 

Catalysts in Social Change: The Metaphorical Application
Beyond the scientific realm, the concept of a catalyst is often used metaphorically to describe a person or event that sparks change. Just as a chemical catalyst accelerates a reaction, a social catalyst can spark a transformation in society. This could be a charismatic leader who inspires a movement, a groundbreaking invention that revolutionizes an industry, or a pivotal event that triggers societal change.

 

The role of a catalyst in social change is to initiate and accelerate the transformation process. They challenge the status quo, inspire action, and provide a pathway for change. However, like chemical catalysts, they are not consumed or altered in the process. Instead, they spark a reaction that continues beyond their involvement.

 

Catalysts in Personal Growth: The Transformative Influence
Similarly, in personal growth, a catalyst can be a life-changing event, a powerful conversation, or a profound insight that triggers transformation. These catalysts challenge our beliefs, push us out of our comfort zones, and spark personal growth and development.

 

The role of a catalyst in personal growth is to initiate a process of self-reflection and change. They provide a new perspective, challenge our assumptions, and inspire us to take action. However, the change ultimately comes from within, and the catalyst merely facilitates this process.

 

In conclusion, the role of catalysts is multifaceted and significant. In chemistry and biology, they facilitate essential reactions and sustain life. In social change and personal growth, they spark transformation and accelerate progress. Whether literal or metaphorical, catalysts play a vital role in accelerating change and driving progress in various domains. By understanding the role of catalysts, we can harness their power to drive change, foster growth, and transform our world.

 

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Efficient reaction type equilibrium catalyst/Reactive equilibrium catalyst
Dabco amine catalyst/Low density sponge catalyst
High efficiency amine catalyst/Dabco amine catalyst
Non-emissive polyurethane catalyst/Dabco NE1060 catalyst
Dabco NE1060/Non-emissive polyurethane catalyst
NT CAT BDMA
NT CAT PC-9