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Rosephenone

Rosephenone structure

Rosephenone 

structure
  • CAS No:

    90-17-5

  • Formula:

    C10H9Cl3O2

  • Chemical Name:

    Rosephenone

  • Synonyms:

    Benzenemethanol,α-(trichloromethyl)-,1-acetate;Benzyl alcohol,α-(trichloromethyl)-,acetate;Benzenemethanol,α-(trichloromethyl)-,acetate;Rosacetol;(Trichloromethyl)phenylcarbinyl acetate;Rosetone;(±)-α-(Trichloromethyl)benzyl acetate;Rosone;α-(Trichloromethyl)benzyl acetate;Rosephenone;2,2,2-Trichloro-1-phenylethyl acetate;NSC 165582;2-Acetoxy-1,1,1-trichloro-2-phenylethane;Crystal rose;Rosacetate;Rosinol Cryst;126753-06-8;39347-18-7

  • Categories:

    Cosmetic Ingredient  >  Perfuming

Description

white powder 2,2,2-Trichloro-1-phenylethyl acetate forms white crystals (mp 88 °C) and has a weak, very natural, lasting rose odor.
The ester is prepared from ??-trichloromethylbenzyl alcohol, for example, by reaction with acetic anhydride. The alcohol can be prepared by one of the following methods:
1) Addition of trichloroacetaldehyde (chloral) to benzene in the presence of aluminum chloride.
2) Reaction of benzaldehyde with chloroform in the presence of potassium hydroxide.

DryPowder; PelletsLargeCrystals


Alpha-Trichloromethylbenzyl acetate is a carboxylic ester. It derives from a benzyl alcohol.

Rosephenone Basic Attributes

267.54

267.54

201-972-0

165582

DTXSID2047725

Characteristics

26.30000

3.66

DryPowder; PelletsLargeCrystals

1.4±0.1 g/cm3

89 °C

282°C(lit.)

145.1±25.5 °C

1.546

LD50 orl-rat: 6800 mg/kg FCTXAV 13,681,75

Safety Information

NONH for all modes of transport

2

AJ8375000

Stable. Incompatible with strong oxidizing agents.

P264, P273, P280, P302+P352, P321, P332+P313, P362, P501

H315

|Warning|H315 (99.43%): Causes skin irritation [Warning Skin corrosion/irritation]|P264, P273, P280, P302+P352, P321, P332+P313, P362, and P501|Aggregated GHS information provided by 1637 companies from 6 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Rosephenone Use and Manufacturing

Methods of Manufacturing

Slowly add powdered caustic potash to the mixture of benzaldehyde and chloroform ether, stir and cool the reaction and let it stand for 24 hours, and then fractionate under reduced pressure to collect 145-160℃ (3.33kPa) fractions to obtain trichloromethyl benzyl alcohol , And then heated to reflux with acetyl chloride for 5h, and then rectified to obtain the finished product.

Uses

Used to prepare rose, gerbera fragrance cosmetics and soap essence


Odor agents


Air care products

Production

100,000 - 500,000 lb

Soap, cleaning compound, and toilet preparation manufacturing|Benzenemethanol, .alpha.-(trichloromethyl)-, 1-acetate: ACTIVE

Computed Properties

Molecular Weight:267.5
XLogP3:3.5
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:265.966813
Monoisotopic Mass:265.966813
Topological Polar Surface Area:26.3
Heavy Atom Count:15
Complexity:219
Undefined Atom Stereocenter Count:1
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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