itaconic acid

Itaconic acid structural formula

Structural formula

Business number 02CJ
Molecular formula C5H6O4
Molecular weight 130.1
label

methylene succinic acid,

methinesuccinic acid,

2-Propylene-1,2-dicarboxylic acid,

methylene succinic acid,

Methyl succinic acid,

Methylenesuccinicaci,

3-Carboxy-3-butenoic acid,

2-Propene-1,2-dicarboxylic acid,

Propylenedicarboxylic acid,

sour agent,

pH regulator,

metal chelating agents,

acidic solvent

Numbering system

CAS number:97-65-4

MDL number:MFCD00004260

EINECS number:202-599-6

RTECS number:None

BRN number:1759501

PubChem number:24881763

Physical property data

1. Properties: white crystalline powder, with special odor and hygroscopicity.

2. Density (g/mL, 20?): 1.632

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

4. Melting point (ºC): 175

5. Boiling point (ºC, normal pressure): 268 (sublimation)

6. Crystal phase standard combustion heat (enthalpy) (kJ ·mol-1): -1983.93

7. Crystal phase standard claims heat (enthalpy) (kJ·mol-1): -841.11

8. Flash point (ºC): 198.7

9. Specific rotation (º): Undetermined

10. Autoignition point or ignition temperature (ºC ): 800

11. Vapor pressure (mmHg, ºC): Undetermined

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

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

14. Critical temperature (ºC): Undetermined

15. Critical pressure (KPa): Undetermined

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

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

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

19. Solubility: Slightly soluble in benzene, chloroform, ether, petroleum ether, carbon disulfide, soluble in water, ethanol, and acetone.

Toxicological data

None

Ecological data

This substance is harmful to the environment, and special attention should be paid to the pollution of water bodies.

Molecular structure data

1. Molar refractive index: 27.91

2. Molar volume (cm3/mol): 95.2

3. Isotonic specific volume (90.2K ): 259.8

4. Surface tension (dyne/cm): 55.4

5. Polarizability (10-24cm3): 11.06

Compute chemical data

1. Hydrophobic parameter calculation reference value (XlogP): -0.1

2. Number of hydrogen bond donors: 2

3. ?Number of bonded receptors: 4

4. Number of rotatable chemical bonds: 3

5. Number of tautomers:

6. Topological molecular poles Physical surface area (TPSA): 74.6

7. Number of heavy atoms: 9

8. Surface charge: 0

9. Complexity: 158

10. Number of isotope atoms: 0

11. Number of determined atomic stereocenters: 0

12. Number of uncertain atomic stereocenters: 0

13. The number of determined stereocenters of chemical bonds: 0

14. The number of uncertain stereocenters of chemical bonds: 0

15. The number of covalent bond units: 1

Properties and stability

1. Avoid contact with alkalis and oxidants.

2.This product has low toxicity and is not harmful to health, but its vapor is toxic. During production, equipment should be sealed and operators should wear protective gear.

3. The chemical properties are relatively active and can be polymerized by itself or with different numbers of other monomers such as propylene. Polymerization of nitriles, styrene, etc. The vapor is toxic and can easily decompose if overheated.

4. Exist in smoke.

Storage method

Sealed packaging. Store in a cool, dry place away from light. It needs to be put into paper buckets lined with plastic bags and stored tightly. Pay attention to moisture, heat and oxidation protection. Store and transport according to general chemical regulations.

Synthesis method

1. There are two types of chemical synthesis methods and industrial fermentation methods. Most manufacturers use industrial fermentation methods for production. The fermentation method mainly uses starch, sucrose, molasses, sawdust, rice straw and other agricultural and sideline products as raw materials, uses sugar as the culture medium, adds nitrogen sources and inorganic salts, and uses Aspergillus terreus as the strain. After two days of fermentation, it is filtered, concentrated, decolorized, and crystallized. , obtained by drying.

2.Heat the concentrated citric acid aqueous solution to 280~300? under reduced pressure (4.0~5.3kPa) to decompose itaconic anhydride and itaconic acid, and then separate and extract itaconic acid from them.

3. Synthesized from propargyl chloride, carbon monoxide, carboxynickel and water.

Purpose

1. Can be used as sour agent, pH regulator, and metal chelating agent. It is an important intermediate in the chemical synthesis industry and can be used to produce synthetic resins, rubber, plastics, lubricant additives, boiler descalers, adhesives, detergents, herbicides, etc. Its esters are also important raw materials for plastic plasticizers.

2.In recent years, more and more research and applications have been conducted on the synthesis of copolymers using itaconic acid as a monomer. One of the important aspects is the use of itaconic acid as a monomer. Conic acid copolymer is used as water treatment agent and chemical cleaning agent. Itaconic acid and acrylic acid or methacrylic acid are polymerized by aqueous solution polymerization to obtain a copolymer with a relative molecular mass of 500 to 200,000. Copolymers with different relative molecular weights and compositions are different properties and uses.
Itaconic acid-acrylic acid copolymer (mass ratio 90:10) is used for online cleaning of circulating cooling water systems, and can effectively remove thick scale layers (0.01~1.7 mm thick). Hard scale containing 67% hydroxyapatite and 13% magnesium silicate adhered to the heating surface. It was treated with 100 mg/L itaconic acid-acrylic acid copolymer (mass ratio 90:10), and the scale removal rate reached 90%. When treated with sodium polyacrylate (average relative molecular weight: 4500), the scale removal rate was only 15.2%. Its descaling characteristics are: it can be carried out while the equipment is running normally, the cleaning conditions are mild, there is no need to add acid to lower the PH value, and the cleaning time is slightly longer (generally 10 to 60 days).

3. As a comonomer of polyacrylonitrile, its synthetic fibers can improve the dyeing properties of synthetic fibers. It can also be used to prepare plasticizers, lubricant additives, dispersion latex for coatings, etc.

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6-acetamidocaproic acid

6-acetamidocaproic acid structural formula

Structural formula

Business number 018A
Molecular formula C8H15NO3
Molecular weight 173.21
label

6-Aminocaproic acid

Numbering system

CAS number:57-08-9

MDL number:MFCD00004424

EINECS number:200-310-8

RTECS number:None

BRN number:None

PubChem ID:None

Physical property data

1. Characteristics: white crystal .


2. Density (g/mL,25/4?) ? Undetermined


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


4. Melting point (ºC): 104?105.5


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


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


7. Refractive index: not OK


8. Flashpoint (ºC): Undetermined


9. Specific optical rotation ( º): Undetermined


10. Spontaneous ignition point or ignition Combustion temperature (ºC): not OK


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. Oil and water (octanol /Water) partition coefficient pair Value: Undetermined


17. Explosion upper limit (%,V/V): not OK


18. Lower explosion limit (%,V/V): not OK


19. Solubility: Not available Sure.

Toxicological data

None

Ecological data

None

Molecular structure data

5. Molecular property data:


1. Molar refractive index: 44.30


2. Molar volume (m3/mol??161.1


3. isotonic specific volume (90.2K):405.2


4. Surface tension (dyne/cm??39.9


5. Polarizability?10-24cm3):17.56

Compute chemical data

1. Reference value for hydrophobic parameter calculation (XlogP): 0.1


2. Number of hydrogen bond donors: 2


3. Number of hydrogen bond acceptors: 3


4. Number of rotatable chemical bonds: 6


5. Number of tautomers: 2


6. Topological molecular polar surface area (TPSA):66.4


7. Number of heavy atoms: 12


8. Surface charge: 0


9. Complexity: 156


10. Number of isotope atoms: 0


11. Determine the number of atomic stereocenters: 0


12. Uncertain number of stereocenters: 0


13. Determine the number of stereocenters of chemical bonds: 0


14. Uncertain number of chemical bond stereocenters: 0


15. Number of covalent bond units: 1

Properties and stability

None

Storage method

This product should be kept sealed.

Synthesis method

None

Purpose

Pharmaceutical intermediates.

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Ethyl lactate

Ethyl lactate structural formula

Structural formula

Business number 02CH
Molecular formula C5H10O3
Molecular weight 118.13
label

2-Hydroxyethylpropionate,

a-hydroxypropionate ethyl ester,

Ethyl a-hydroxypropionate,

Ethyl L-lactate,

2-Hydroxypropanoic acid ethyl ester,

Flavors and fragrances

Numbering system

CAS number:97-64-3

MDL number:MFCD00004518

EINECS number:202-598-0

RTECS number:OD5075000

BRN number:1209448

PubChem number:24901084

Physical property data

1. Properties: colorless transparent liquid with slight odor. [1]

2. Melting point (?): -26[2]

3. Boiling point (?): 154[3]

4. Relative density (water = 1): 1.03[4]

5. Relative vapor Density (air=1): 4.07[5]

6. Saturated vapor pressure (kPa): 0.5 (25?)[6]

7. Heat of combustion (kJ/mol): -3190.1[7]

8. Critical pressure (MPa): 3.86[8]

9. Octanol/water partition coefficient: -0.18[9]

10. Flash point (?): 46.1 (CC )[10]

11. Ignition temperature (?): 400[11]

12. Explosion upper limit ( %): 10.6[12]

13. Lower explosion limit (%): 1.5[13]

14. Dissolution Properties: Miscible with water, miscible in alcohols, esters, ketones, hydrocarbons, and oils. [14]

Toxicological data

1. Acute toxicity: rat oral LD50: >5mg/kg; rat peritoneal cavity LDL0: 1mg/kg; mouse oral LD50: 2500mg/kg; mouse subcutaneous LD50: 2500mg/kg; mouse Intravenous injection LD50: 600mg/kg; rabbit skin contact LD50: >5mg/kg; guinea pig muscle LDL0: 2605mg/kg;

2. Acute toxicity [15] LD50: 2500mg/kg (orally administered to mice)

3. Irritation No information available

Ecological data

1. Ecotoxicity No data available

2. Biodegradability No data available

3 .Non-biodegradability No information available

Molecular structure data

1. Molar refractive index: 28.48

2. Molar volume (cm3/mol): 112.4

3. Isotonic specific volume (90.2K ): 269.9

4. Surface tension (dyne/cm): 33.2

5. Polarizability (10-24cm3): 11.29

Compute chemical data

1. Reference value for hydrophobic parameter calculation (XlogP): 0.2

2. Number of hydrogen bond donors: 1

3. Number of hydrogen bond acceptors: 3

4. Number of rotatable chemical bonds: 3

5. Number of tautomers: none

6. Topological molecule polar surface area 46.5

7. Number of heavy atoms: 8

8. Surface charge: 0

9. Complexity: 79.7

10. Number of isotope atoms: 0

11.??Determine the number of atomic stereocenters: 0

12. Uncertain number of atomic stereocenters: 1

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[16] Stable

2. Incompatible substances[17] Strong oxidants, acids, alkalis

3. Polymerization hazard[18] No polymerization

Storage method

Storage Precautions[19] Store in a cool, ventilated warehouse. The storage temperature should not exceed 37°C and should be kept away from fire and heat sources. Keep container tightly sealed. They should be stored separately from oxidants, acids, and alkalis, 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. Metal halide catalysis method. Using metal halide instead of concentrated sulfuric acid to catalyze the synthesis of ethyl lactate, the yield is 65%-71%.

2. Rare earth compound catalysis method. Add 0.22-0.33 mol of ethanol, 0.11 mol of lactic acid, 25 mL of water-carrying agent and rare earth compound (molar ratio to acid is 1:100) into the flask, reflux for 2.5-3 hours, and evaporate excess ethanol, water-carrying agent and rare earth compounds from the reaction solution. The unreacted lactic acid is then distilled under reduced pressure and the product is collected with a yield of 74%-79%.

3. Sulfuric acid catalysis method. Lactic acid is esterified with excess ethanol under the catalysis of sulfuric acid to obtain ethyl lactate; it can also be heated in carbon tetrachloride to effluent for 24 hours, distilled under normal pressure to recover excess ethanol, and then distilled under reduced pressure to obtain the finished product.

4. Solid acid catalysis method. The NaY molecular sieve is washed with water, dried, and burned at high temperature, and then stirred and impregnated with a certain concentration of NH4Cl solution to perform ion exchange. The NH4Y is filtered, washed, dried, and activated at 550°C to obtain the solid acid HY. Then add lactic acid, ethanol, benzene, and HY into the reaction bottle, HY/lactic acid (mass ratio) = 25/100, lactic acid/ethanol (molar ratio) = 1/3. After reflux and water separation reaction at 100-160°C for 8-10 hours, the esterification rate is over 60%.

5. Distillation esterification method. Add 225g of 80% lactic acid, 475Ml (380g) of 95% ethanol, 100mL of benzene, 2 mL of concentrated sulfuric acid and a little zeolite into the flask (1000 mL) of the water distillation device. Add the reaction solution until it boils. The steam (ethanol, benzene and water) passes through the distillation column and enters the condenser. The water layer is separated and then flows back to the distillation column. The temperature at the top of the column is stable at 64.9°C. When 240g of water layer is separated (which contains 119g of ethanol, 99g of water, and 22g of benzene), almost no water separates out. When the temperature at the top of the column rises to 68°C, the esterification is completed. After cooling the reaction solution, add 6 g of anhydrous sodium acetate to neutralize sulfuric acid, and perform distillation under reduced pressure. First, complete reflux for 1 hour, then under a vacuum of 2.45Kpa, control the reflux ratio to not less than 5, and the column top temperature to 58°C, to distill 226g of colorless and clear ethyl lactate, with a yield of 96%.

6. It is obtained by esterification of lactic acid and excess ethanol under the action of catalyst, and then refined.

Purpose

1. Mainly used for blending apple, pineapple, caramel, frankincense and other food flavors, and also used in wine flavors such as rum and liquor. Ethyl lactate is a food flavoring allowed in my country. Generally, it is 1000mg/kg in alcoholic beverages; 580-3100mg/kg in chewing gum; 71mg/kg in baked goods; 28mg/kg in candies; and 17mg/kg in cold drinks.

2. Used as a solvent for cellulose esters, resins, coatings, etc., and also used as perfume. [20]

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PRODUCT