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17369-57-2

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17369-57-2 Usage

Description

3-Methylbenzyl acetate, also known as 3-methylphenyl acetate, is an organic compound with the chemical formula C9H10O2. It is a clear colorless liquid characterized by a sweet, fruity, and floral odor, reminiscent of jasmine and apple. This chemical is widely recognized for its pleasant aroma and is commonly used in the fragrance and flavor industry as a scent ingredient.
Used in Fragrance Industry:
3-Methylbenzyl acetate is used as a scent ingredient for its sweet, fruity, and floral odor, which closely resembles the scent of jasmine and apple. Its pleasant aroma makes it a popular choice in the creation of perfumes, colognes, and other fragrance products.
Used in Flavor Industry:
In the flavor industry, 3-Methylbenzyl acetate is used as a flavoring agent to impart a sweet and fruity taste to various food and beverage products, enhancing their overall flavor profile.
Used in Industrial Applications:
3-Methylbenzyl acetate also serves as a solvent in a range of industrial applications. Its solvent properties make it a useful component in the manufacturing process of various products, including cosmetics and other consumer goods.
Used in Cosmetics:
In the cosmetics industry, 3-Methylbenzyl acetate is used as a fragrance ingredient to add a pleasant scent to products such as lotions, creams, and perfumes. Its use in small quantities is considered relatively safe, but care should be taken to avoid skin and eye irritation that may occur with high concentrations.
It is important to handle 3-Methylbenzyl acetate with care, as it may cause skin and eye irritation in high concentrations. However, when used responsibly and in appropriate amounts, it offers a variety of applications across different industries, making it a valuable component in the creation of fragrances, flavors, and other products.

Check Digit Verification of cas no

The CAS Registry Mumber 17369-57-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,3,6 and 9 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 17369-57:
(7*1)+(6*7)+(5*3)+(4*6)+(3*9)+(2*5)+(1*7)=132
132 % 10 = 2
So 17369-57-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H12O2/c1-8-4-3-5-10(6-8)7-12-9(2)11/h3-6H,7H2,1-2H3

17369-57-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (3-methylphenyl)methyl acetate

1.2 Other means of identification

Product number -
Other names EINECS 241-401-2

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:17369-57-2 SDS

17369-57-2Relevant articles and documents

Bu 4 NI-Catalyzed C-C Bond Cleavage and Oxidative Esteri??cation of Allyl Alcohols with Toluene Derivatives

Chen, Yaoyao,Cui, Yongmei,Jia, Xueshun,Li, Chengliang,Li, Jian,Sun, Mingming

, p. 3667 - 3674 (2019/09/30)

A novel oxidative esterification of 1-arylprop-2-en-1-ols with toluene derivatives catalyzed by tetrabutylammonium iodide (TBAI) is reported. The optimization of the reaction conditions illustrates that each of experiment parameters including the catalyst, solvent, and oxidant is significant for present oxidative functionalization. This metal-free protocol has a broad substrate scope including the halogen groups for further functionalization and enriches the reactivity profile of allyl alcohol and toluene derivatives. In addition, this protocol represents a new transformation of allyl alcohol involving C-C bond cleavage and C-O bond forming.

Supported palladium nanoparticles as switchable catalyst for aldehyde conjugate/s and acetate ester syntheses from alcohols

Kumar, Sandeep,Chaudhary, Abha,Bandna,Bhattacherjee, Dhananjay,Thakur, Vandna,Das, Pralay

supporting information, p. 3242 - 3245 (2017/07/12)

Polymer-supported Pd(0) (Pd@PS) nanoparticles (NPs) were explored as a switchable catalyst for oxidative aldehyde conjugate/s (AC/s) and acetate esters (AEs) syntheses from alcohols. Using the same substrates, the catalyst in the presence of oxygen and K2CO3 participated in AC/s synthesis, and in the presence of traces of air and NaOtBu, unusual AEs products were obtained.

Polystyrene trimethyl ammonium chloride impregnated Rh(0) (Rh@PMe3NCl) as a catalyst and methylating agent for esterification of alcohols through selective oxidation of methanol

Guha, Nitul Ranjan,Bhattacherjee, Dhananjay,Das, Pralay

, p. 2575 - 2580 (2015/06/30)

Rhodium(0) nanoparticle (NP)-impregnated polystyrene trimethyl ammonium chloride (PMe3NCl) resin (Rh@PMe3NCl) under basic conditions acts as a cross-dehydrogenative coupling-methylating (CDCM) agent for the selective oxidation of methanol and its in situ reaction with benzyl/alkyl alcohols allowing methyl group transfer for acetate ester synthesis in a tandem approach. The redox property of methanol which restricts the oxidation of benzyl/alkyl alcohols for product formation is critically investigated.

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