Bromoform

Bromoform structural formula

Structural formula

Business number 01JA
Molecular formula CHBr3
Molecular weight 252.73
label

Bromoform,

Methyl tribromide,

Tribromomethane,

Formyltribromide,

Aliphatic halogenated derivatives

Numbering system

CAS number:75-25-2

MDL number:MFCD00000128

EINECS number:200-854-6

RTECS number:PB5600000

BRN number:1731048

PubChem number:24863014

Physical property data

1. Properties: Colorless heavy liquid with a chloroform-like smell. [1]

2. Melting point (ºC): 6~9[2]

3. Boiling point (ºC) : 149.5[3]

4. Relative density (water = 1): 2.89[4]

5. Relative Vapor density (air=1): 8.7[5]

6. Saturated vapor pressure (kPa): 0.75 (25ºC)[6]

7. Critical pressure (MPa): 6.09[7]

8. Octanol/water partition coefficient: 2.38[8]

9. Solubility: Slightly soluble in water, soluble in ethanol, ether, chloroform, benzene, etc. [9]

10. Specific heat capacity (KJ/(kg·K), 18~50ºC, constant pressure): 0.519

11. Electrical conductivity ( S/m, 25ºC): <2×10-8

12. Vapor pressure (kPa, 22ºC): 0.67

13. Vapor pressure ( kPa, 48ºC): 2.67

14. Volume expansion coefficient (K-1): 0.00091

15. Refractive index at room temperature (n20 ): 1.5976

16. Refractive index at room temperature (n25): 1.5956

17. Lennard-Jones parameter (A): 8.153

18. Lennard-Jones parameter (K): 162.2

19. Solubility parameter (J·cm-3)0.5 sup>: 21.726

20. van der Waals area (cm2·mol-1): 6.810×109

21. van der Waals volume (cm3·mol-1): 49.980

22. Gas phase standard entropy (J·mol-1·K-1): 330.70

23. Gas phase standard hot melt (J·mol-1·K-1): 70.98

24. Liquid phase standard hot melt (J·mol-1·K– 1): 129.9

Toxicological data

1. Acute toxicity[10]

LD50: 933mg/kg (rat oral); 414mg/kg (rat intraperitoneal ); 1072mg/kg (orally administered to mice)

LC50: 12100mg/m3 (inhaled to mice, 2h)

2. Irritation No data available

3. Subacute and chronic toxicity [11] Rat inhalation 0.25mg/L, 4 hours a day , 2 months later, abnormal liver and kidney function.

4. Mutagenicity [12] Microbial mutagenicity: Salmonella typhimurium 50?l/dish. Sister chromatid exchange: human lymphocytes 80 ?mol/L. DNA damage: human lung 100 ?mol/L (3h).

5. Teratogenicity[13] Mice were orally administered the lowest toxic dose (TDLo) 200mg/kg for many generations, causing hepatobiliary and Developmental malformations of the genitourinary system.

6. Carcinogenicity[14] IARC Carcinogenicity Comment: G3, insufficient evidence of carcinogenicity to humans and animals.

Ecological data

1. Ecotoxicity[15] LC50: 40.4mg/L (48h) (medaka)

2. Biology Degradability[16]

Aerobic biodegradation (h): 672~4320

Anaerobic biodegradation (h): 2688 ~17280

3. Non-biodegradability[17]

Photooxidation half-life in air (h): 1299~ 12989

First-order hydrolysis half-life (h): 6.02×106

4. Bioaccumulation [18] BCF: 7.1~21 (carp, exposure concentration 100mg/L, exposure time 6 weeks); 7.7~19 (carp, exposure concentration 10mg/L, exposure time 6 weeks)

5. Other harmful effects[19] It decomposes when exposed to alkali, but it is a highly persistent compound in water and will not be biodegraded. Especially if it stays in drinking water for a long time, it will cause harm.

Molecular structure data

1. Molar refractive index: 29.83

2. Molar volume (cm3/mol): 84.9

3. Isotonic specific volume (90.2K ): 225.7

4. Surface tension (dyne/cm): 49.8

5. Polarizability (10-24cm3): 11.82

Compute chemical data

1. Reference value for hydrophobic parameter calculation (XlogP): 2.8

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: 4

8. Surface charge: 0

9. Complexity: 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. Stability[20] Stable

2. Incompatible substances[21] Strong oxidants, active metal powders

3. Conditions to avoid contact[22] Light

4.Polymerization hazard[23] No polymerization

5. Diversity products[24] Bromine Hydrogen

Storage method

Storage Precautions[25] Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature does not exceed 32°C and the relative humidity does not exceed 80%. Keep container tightly sealed. They should be stored separately from oxidants, active metal powders, and food chemicals, and avoid mixed storage. The storage area should be equipped with emergency release equipment and suitable containment materials.

Synthesis method

1. Under alkaline conditions, acetone reacts with sodium hypobromite to obtain tribromoacetone, which will continue to decompose under alkaline conditions to obtain crude product. After distillation, washing, filtering and drying, the finished product is obtained.

Purpose

1. It can be used as dye intermediates, disinfectants, analgesics, anesthetics, refrigerants, mineral processing agents, precipitants, solvents and anti-explosion liquid components.

2. Used as solvent, refractive index liquid and specific gravity liquid.

3. Used as solvent and organic synthesis intermediate. [26]

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Allyl isothiocyanate

Propylene isothiocyanate structural formula

Structural formula

Business number 0189
Molecular formula C4H5NS
Molecular weight 99.16
label

3-isothiocyanato-1-propene; artificial mustard oil,

3-Different thiocyanomethylthio-1-acrylamide,

Artificial mustard oil,

Allyl isothiocyananate,

Isothiocyanic acid allyl ester,

iso-Thiocyanic acid allyl ester,

artificial flavors

Numbering system

CAS number:57-06-7

MDL number:MFCD00004822

EINECS number:200-309-2

RTECS number:NX8225000

BRN number:773748

PubChem number:24862709

Physical property data

1. Properties: colorless or light yellow oily liquid with pungent odor. [1]

2. Melting point (?): -80[2]

3. Boiling point (?): 150.7[3]

4. Relative density (water = 1): 1.01[4]

5. Relative vapor Density (air=1): 3.41[5]

6. Saturated vapor pressure (kPa): 1.33 (38.3?)[6]

7. Octanol/water partition coefficient: 2.11[7]

8. Flash point (?): 46 (CC)[8 ]

9. Solubility: Slightly soluble in water, miscible in most organic solvents such as ethanol, ether, carbon disulfide, etc. [9]

10. Refractive index (n20/D): 1.527-1.531

Toxicological data

1. Acute toxicity[10] LD50: 112mg/kg (rat oral); 88mg/kg (rabbit dermal)

2. Irritation [11] Rabbit transdermal; 2 mg, causes irritation.

3. Mutagenicity [12] Microbial mutagenicity: Salmonella typhimurium 100?g/dish. Mammalian somatic mutations: mouse lymphocytes 400 ?g/L. Cytogenetic analysis: Hamster ovary 5mg/L. Sister chromatid exchange: Hamster ovary 160?g/L. DNA damage: human ascites tumor 50?mol/L (24h)

4. Carcinogenicity [13] IARC Carcinogenicity Comment: G3, for humans and There is insufficient evidence of carcinogenicity in animals.

5. Others[14] Rat subcutaneous minimum toxic dose (TDLo): 100mg/kg (gestation 8~9d), causing embryotoxicity (embryonic development retardation)

Ecological data

1. Ecotoxicity[15] LC50: 0.0856mg/L (96h) (fathead minnow, dynamic)

2. Biodegradability No data available

3. Non-biodegradability No data available

Molecular structure data

1. Molar refractive index: 31.17

2. Molar volume (cm3/mol): 108.8

3. Isotonic specific volume (90.2K ): 249.8

4. Surface tension (dyne/cm): 27.7

5. Polarizability (10-24cm3???12.35

Compute chemical data

1. Reference value for hydrophobic parameter calculation (XlogP): 2.4

2. Number of hydrogen bond donors: 0

3. Number of hydrogen bond acceptors: 1

p>

4. Number of rotatable chemical bonds: 2

5. Number of tautomers:

6. Topological molecular polar surface area (TPSA): 12.4

p>

7. Number of heavy atoms: 6

8. Surface charge: 0

9. Complexity: 81.5

10. Number of isotope atoms : 0

11. Determine the number of atomic stereocenters: 0

12. Uncertain number of atomic stereocenters: 0

13. Determine the chemical bond configuration Number of centers: 0

14. Number of uncertain chemical bond stereocenters: 0

15. Number of covalent bond units: 1

Properties and stability

1. Colorless to light yellow transparent oily liquid, the color gradually turns darker during storage. It has a strong mustard-like pungent odor and spicy taste. No optical activity. Miscible in ethanol, ether and carbon disulfide. It has anti-fungal and bactericidal effects.

2. Stability[16] Stable

3. Incompatible substances[17] Water, alcohols, strong bases, amines, acids, strong oxidants

4. Conditions to avoid contact[18] Humid air

5. Polymerization hazard[19] Polymerization

6. Decomposition products[20] Hydrogen cyanide, sulfide

Storage method

Storage Precautions[21] Stored in a cool, dry and well-ventilated special warehouse, and implement “two people to send and receive, two people to keep” “system. Keep away from fire and heat sources. The packaging must be sealed and must not come into contact with air. They should be stored separately from oxidants, acids, alkalis, 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 emergency release equipment and suitable containment materials.

Synthesis method

1. Dissolve allyl iodide or allyl bromide and potassium thiocyanate in ethanol and heat. After the potassium halide is completely precipitated, add water to precipitate allyl isothiocyanate, and distill and refine. The actual yield is 65%-70% of the theoretical value.

Purpose

1. Used for spices. In the manufacture of military uniform poison gas, ointment is used as a counter-irritant. GB 2760–1996 stipulates that food spices are temporarily allowed to be used. Mainly used for preparing spices and mustard-type flavors for pickles, cans, sauces, seasonings, etc.

2. Used to prepare food additives, medicines, pesticides, fungicides, etc.

3. Used as fumigant, military poison gas, etc. [22]

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Ethyl methacrylate

Ethyl methacrylate structural formula

Structural formula

Business number 02CG
Molecular formula C6H10O2
Molecular weight 114.14
label

Ethyl-2-methyl-2-acrylate,

Ethyl methacrylate,

Ethyl methacrylate,

Ethyl methacrylate,

2-Ethyl methacrylate,

Ethyl methacrylic acid,

Ethyl methyl acrylate,

Ethyl methacrylate,

2-Methyl-2-propenoic acid ethyl ester,

2-Methylacrylic acid ethyl ester,

EMA,

Methacrylic acid ethyl ester,

aliphatic compounds

Numbering system

CAS number:97-63-2

MDL number:MFCD00009161

EINECS number:202-597-5

RTECS number:OZ4550000

BRN number:471201

PubChem number:24884362

Physical property data

1. Properties: Colorless liquid, easily volatile, with spicy taste. [1]

2. Melting point (?): -75[2]

3. Boiling point (?): 117~119[3]

4. Relative density (water=1): 0.91 (25?)[4]

5. Relative vapor density (air=1): 3.9[5]

6. Saturated vapor pressure (kPa): 2.0 (20?)[6 ]

7. Heat of combustion (KJ/mol): -3356.3[7]

8. Critical pressure (MPa): 3.25 [8]

9. Octanol/water partition coefficient: 1.94[9]

10. Flash point (? ): 20 (OC) [10]

11. Ignition temperature (?): 370[11]

12. Explosion upper limit (%): 9.6[12]

13. Explosion lower limit (%): 1.8[13]

14. Solubility: Slightly soluble in water, miscible in ethanol and ether. [14]

Toxicological data

1. Acute toxicity[15]

LD50: 14800mg/kg (rat oral)

LC50: 8300ppm (rat inhalation, 4h)

2. Irritation No information available

3. Others [16] The lowest toxic dose in the abdominal cavity of rats (TDLo): 735mg/kg (administered on 5th to 15th day of pregnancy), causing embryotoxicity.

Ecological data

1. Ecotoxicity No data available

2. Biodegradability No data available

3 .Non-biodegradable[17] In the air, when the concentration of hydroxyl radicals is 5.00×105/cm3, the degradation half-life is 19h (theoretical).

When the pH value is 11, the hydrolysis half-life is 2.5h.

4. Other harmful effects[18] This substance may be harmful to the environment, and special attention should be paid to water bodies.

Molecular structure data

1. Molar refractive index: 31.18

2. Molar volume (cm3/mol): 125.9

3. Isotonic specific volume (90.2K ): 280.7

4. Surface tension (dyne/cm): 24.6

5. Polarizability: 12.36

Compute chemical data

1. Reference value for hydrophobic parameter calculation (XlogP): 1.9

2. Number of hydrogen bond donors: 0

3. Number of hydrogen bond acceptors: 2

4. Number of rotatable chemical bonds: 3

5. Number of tautomers:

6. Topological molecular polar surface area (TPSA): 26.3

7. Number of heavy atoms: 8

8. Surface charge: 0

9. Complexity: 105

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 Number: 0

14. Number of uncertain chemical bond stereocenters: 0

15. Number of covalent bond units: 1

Properties and stability

1. The toxicity of this product is similar to that of methyl methacrylate, and the oral LD50 is 15mL/kg. The protection requirements are the same as those for methyl methacrylate. See methyl methacrylate.

2. Stability[19] Stable

3. Incompatible substances[20] Strong oxidants, strong acids, strong alkali

4. Conditions to avoid contact [21] Heat, light, ultraviolet rays , contact with air

5. Polymerization hazard[22] Polymerization

Storage method

Storage Precautions[23] Usually products contain polymerization inhibitors. Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Keep away from light. The storage temperature should not exceed 37?. The packaging must be sealed and must not come into contact with air. They should be stored separately from oxidants, acids, and alkalis, and avoid mixed storage. It should not be stored in large quantities or for long periods of time. 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. Obtained from the esterification of methacrylic acid and ethanol.

Combine methacrylic acid and anhydrous Add ethanol to the reaction pot, add a small amount of concentrated sulfuric acid, and heat and reflux until an ester layer appears. Cool, separate the ester layer, wash with alkali, water, dry, and then fractionate under reduced pressure to obtain the product. The content of industrial product ethyl methacrylate is ?98%. Raw material consumption quota: methacrylic acid 950kg/t, ethanol 900kg/t.

2. Acetone cyanohydrin reacts with sulfuric acid to form methacrylamide, which is then hydrolyzed and esterified with ethanol to obtain a crude product, which is then dehydrated and distilled to obtain the finished product.

Purpose

1. Commonly used polymerized monomers. It can be used as an intermediate for adhesives, coatings, fiber treatment agents, and molding materials. It can also be used to make acrylic copolymers. It can be copolymerized with methyl methacrylate to improve its brittleness. It is also used to make organic glass, synthetic resin and molding powder.

2. Used to prepare polymers and copolymers, synthetic resins, organic glass and coatings, etc. [24]

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PRODUCT