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4-Methoxybenzyl acetate

4-Methoxybenzyl acetate structure

4-Methoxybenzyl acetate 

structure
  • CAS No:

    104-21-2

  • Formula:

    C10H12O3

  • Chemical Name:

    4-Methoxybenzyl acetate

  • Synonyms:

    Benzenemethanol,4-methoxy-,1-acetate;Benzyl alcohol,p-methoxy-,acetate;Benzenemethanol,4-methoxy-,acetate;p-Anisyl alcohol,acetate;Cassie ketone;p-Methoxybenzyl acetate;p-Methoxybenzyl alcohol acetate;4-Methoxybenzyl acetate;4-Methoxybenzenemethanol acetate;NSC 46102;4-Anisyl acetate;1-Methoxy-4-acetoxymethylbenzene;(4-Methoxyphenyl)methyl acetate

  • Categories:

    Cosmetic Ingredient  >  Perfuming

Description

Solid


Liquid|Solid|colourless to pale yellow liquid with a floral, fruity, balsamic odour

4-Methoxybenzyl acetate Basic Attributes

180.2

180.20

203-185-8

2GEC7KBO31

46102

DTXSID1044770

2915390090

Characteristics

35.5

1.9

Liquid

1.1±0.1 g/cm3

84 °C

270 °C

>230 °F

1.500

insoluble in water, glycerol, propylene glycol; soluble in organic solvents, oils

Store in a tightly closed container. Store in a cool, dry, well-ventilated area away from incompatible substances.

0.0277mmHg at 25°C

Safety Information

NONH for all modes of transport

2

20/21/22-36/37/38

24/25-36-26

Xn

Stable under normal temperatures and pressures.

P264, P280, P302+P352, P305+P351+P338, P321, P332+P313, P337+P313, P362

H315

|Warning|H315 (92.37%): Causes skin irritation [Warning Skin corrosion/irritation]|P264, P280, P302+P352, P305+P351+P338, P321, P332+P313, P337+P313, and P362|Aggregated GHS information provided by 1682 companies from 8 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Drug Information

anisyl acetate

4-Methoxybenzyl acetate Use and Manufacturing

Methods of Manufacturing

The mixture of anisole and formaldehyde was saturated with hydrogen chloride at 0°C, washed several times in ice water, and gradually added the preheated acetic acid and anhydrous sodium acetate mixture. After the reaction was completed, the acetic acid was removed by distillation. It is obtained by washing with sodium carbonate solution and purifying by distillation under reduced pressure. It is derived from the reaction of p-methoxybenzyl alcohol (anisole) with acetic anhydride.

Uses

It can be used to mix almond, floral and coconut flavors.


Air care products

Production

< 25,000 lb

Benzenemethanol, 4-methoxy-, 1-acetate: ACTIVE

Food additives -> Flavoring Agents|Flavoring Agents -> JECFA Flavorings Index

Flavoring Agents

Computed Properties

Molecular Weight:180.20
XLogP3:1.9
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:180.078644241
Monoisotopic Mass:180.078644241
Topological Polar Surface Area:35.5
Heavy Atom Count:13
Complexity:160
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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