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54553-63-8

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54553-63-8 Usage

Synthesis

It is synthesized by the esterification of benzyl alcohol with acetic acid.

Fragrance and Flavoring Industries

Benzyl acetate is commonly used in the fragrance and flavoring industries.

Aroma

It has a pleasant, sweet floral aroma reminiscent of jasmine or gardenia.

Applications

Perfumes: It is a popular ingredient in perfumes due to its floral scent.
Soaps and Scented Products: Used in soaps and other scented products for its aromatic properties.
Flavoring Agent: It is utilized as a flavoring agent in foods and beverages.

Health Concerns

Irritant: Benzyl acetate can be irritating to the skin, eyes, and respiratory system.
High Concentrations: Exposure to high concentrations may lead to adverse health effects.

Check Digit Verification of cas no

The CAS Registry Mumber 54553-63-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,5,5 and 3 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 54553-63:
(7*5)+(6*4)+(5*5)+(4*5)+(3*3)+(2*6)+(1*3)=128
128 % 10 = 8
So 54553-63-8 is a valid CAS Registry Number.

54553-63-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-acetoxy-2,2-dimethylpropylbenzene

1.2 Other means of identification

Product number -
Other names acetic acid-(2,2-dimethyl-1-phenyl-propyl ester)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:54553-63-8 SDS

54553-63-8Downstream Products

54553-63-8Relevant articles and documents

Carboxylate Anions Accelerate Pyrrolidinopyridine (PPy)-Catalyzed Acylation: Catalytic Site-Selective Acylation of a Carbohydrate by in Situ Counteranion Exchange

Yanagi, Masanori,Imayoshi, Ayumi,Ueda, Yoshihiro,Furuta, Takumi,Kawabata, Takeo

supporting information, p. 3099 - 3102 (2017/06/23)

Acylpyridinium ions have been known as catalytically active species in acylation reactions catalyzed by 4-dimethylaminopyridine and its analogues. Acylpyridinium carboxylates were found to be 800-1300 times more reactive than the corresponding acylpyridin

Barriers to Internal Rotation in Neopentylbenzenes Substituted on the Benzyl Group. A 13C NMR Band Shape Study

Andersson, Sven,Drakenberg, Torbjoern

, p. 730 - 744 (2007/10/02)

Two series of neopentylbenzenes with one or two substituents on the benzyl group have been synthesized.In one series the substituents were H, F, Cl, Br, I, OCH3, OCOCH3, OSi(CH3)3, CH3 and CH2CH3, and in the other OH and R R = H, CH3, CH2CH3, (CH2)3CH3,

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