Epoxy curing agent Knowledge p-Methoxyacetophenone p-Methoxyacetophenone

p-Methoxyacetophenone p-Methoxyacetophenone

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Structural formula of p-methoxyacetophenone

Structural formula

Business number 02H2
Molecular formula C9H10O2
Molecular weight 150.17
label

4′-Methoxyacetophenone,

4-methoxyacetophenone,

Acetyl anisole,

Hawthorn flower ketone,

P-Acetanisole,

4-Methoxyphenylethanone,

4′-Methoxyacetophenone,

p-Methoxyphenyl methylketone

Numbering system

CAS number:100-06-1

MDL number:MFCD00008745

EINECS number:202-815-9

RTECS number:AM9240000

BRN number:742313

PubChem number:24883507

Physical property data

1. Characteristics: Colorless to slightly yellow crystal blocks, with a strong and lasting hay aroma, a somnocin-like aroma, and floral and hawthorn aromas.

2. Relative density (g/mL, 41.1℃): 1.0818

3. Relative density (20℃, 4℃): 1.081841

4. Melting point (ºC): 38~39

5. Boiling point (ºC, normal pressure): 258

6. Boiling point (ºC, 3.5kpa) :152~154

7. Boiling point (ºC, 1.33kpa): 136

8. Flash point (ºC): 138

9. Refractive index(n41D): 1.547

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

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

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

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

19. Solubility: Insoluble in water, soluble in alcohol and ether.

Toxicological data

1. Skin/eye irritation: Standard Dresser test: rabbit skin contact, 500mg/24HREACTION SEVERITY, moderate reaction; 2. Acute toxicity: human inhalation TCL0: 1700μg/m3/39W-I;               Rat oral LD50: 1720mg /kg; Mouse oral LD50: 820mg/kg; Rabbit skin contact LD50: >5mg/kg; 3. Other multiple dose toxicity: Rat inhalation TCLo: 152mg/m3/4H/13W-I;

EcologyData

This substance is slightly hazardous to water.

Molecular structure data

1. Molar refractive index: 42.95

2. Molar volume (cm3/mol): 144.9

3. Isotonic specific volume (90.2K ): 349.1

4. Surface tension (dyne/cm): 33.6

5. Dielectric constant:

6. Dipole moment (10-24cm3):

7. Polarizability: 17.03

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: 2

5. Number of tautomers: 2

6. Topological molecule polar surface area 26.3

7. Number of heavy atoms: 11

8. Surface charge: 0

9. Complexity: 135

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 light and oxides.

2. Found in flue-cured tobacco leaves.

3. Naturally found in beef, sour fruits, and guava.

Storage method

Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Store away from light and tightly packed. should be kept away from oxidizer, do not store together. Use explosion-proof lighting and ventilation facilities. It is prohibited to use mechanical equipment and tools that are prone to sparks. Suitable materials should be available in the storage area to contain spills.

Synthesis method

1. It is prepared by acetylation reaction between anisole and acetic anhydride (or acetyl chloride) under the conditions of anhydrous aluminum trichloride (or ferric chloride, zinc chloride, acidic clay). Add anisole and acetic anhydride to the reaction pot, add zinc chloride and slowly heat to boiling, maintain reflux (about 140°C), react for 4 hours, distill under reduced pressure, wash with water, and rectify to obtain the finished product.

2. Obtained from the reaction of anisole and acetic acid in the presence of boron trifluoride.

3. Obtained from the reaction of anisole and acetyl chloride in the presence of aluminum chloride and carbon disulfide.

4. Tobacco: FC, 18.

Purpose

1. It has a strong hawthorn aroma and is an indispensable raw material for fragrances such as mimosa and hawthorn. It is often used in high-end cosmetics and soap flavors. It has high stability in soap and can also be used as fruit food flavor. . It is also used in organic synthesis to produce p-methoxyphenylacetic acid and is used as an intermediate for puerarin. The dosage in the fragrance formula is within 5%. IFRA has no restrictions. It can be used in edible and tobacco flavor formulations.

2. Used in baked goods, meat products, and candies.

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