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120157-98-4

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120157-98-4 Usage

Description

Carbamic acid, acetyl-, 1,1-dimethylethyl ester (9CI), commonly known as tert-butyl acetate, is a chemical compound with the molecular formula C6H13NO2. It is a colorless liquid with a fruity odor and is flammable. Tert-butyl acetate is widely used as a solvent in various industries and also serves as a flavor and fragrance agent in the food and beverage industry.

Uses

Used in Coatings Industry:
Tert-butyl acetate is used as a solvent in the production of coatings, contributing to the desired properties of the final product, such as drying time, adhesion, and gloss.
Used in Inks Industry:
In the inks industry, tert-butyl acetate is utilized as a solvent to improve the flow and drying characteristics of inks, ensuring consistent application and appearance on various surfaces.
Used in Adhesives Industry:
Tert-butyl acetate serves as a solvent in the formulation of adhesives, enhancing their bonding properties and facilitating better adhesion to different substrates.
Used in Food and Beverage Industry:
As a flavor and fragrance agent, tert-butyl acetate is used in the food and beverage industry to impart specific tastes and aromas to products, enhancing their overall sensory appeal.
Safety Precautions:
It is crucial to handle tert-butyl acetate with care and follow safety guidelines when working with it, due to its potential flammability and reactivity. Proper storage, handling, and disposal practices should be implemented to minimize risks associated with its use.

Check Digit Verification of cas no

The CAS Registry Mumber 120157-98-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,1,5 and 7 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 120157-98:
(8*1)+(7*2)+(6*0)+(5*1)+(4*5)+(3*7)+(2*9)+(1*8)=94
94 % 10 = 4
So 120157-98-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H13NO3/c1-5(9)8-6(10)11-7(2,3)4/h1-4H3,(H,8,9,10)

120157-98-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-Butyl acetylcarbamate

1.2 Other means of identification

Product number -
Other names tert-butyl N-acetylcarbamate

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:120157-98-4 SDS

120157-98-4Relevant articles and documents

New Synthetic Method of Imides through Oxidative Photodecarboxylation Reaction of N-Protected α-Amino Acids with FSM-16

Itoh, Akichika,Kodama, Tomohiro,Inagaki, Shinji,Masaki, Yukio

, p. 542 - 543 (2000)

FSM-16, a mesoporous silica, was found to promote the oxidative photodearboxylation of N-acyl-protected α-amino acids in hexane to afford the corresponding imides.

Deuterium-modified carbapenem derivatives

-

, (2021/01/12)

The invention belongs to the technical field of medicines, and particularly relates to deuterium-modified carbapenem derivatives or pharmaceutically acceptable salts thereof, a method for preparing the compounds, pharmaceutical preparations and pharmaceut

Synthesis of N-Acyl carbamates and oxazolidinones using HClO 4-SiO2 as catalyst under solvent-free conditions

Yang, Li Juan,Yang, Yuping,Dong, Ruoyi

experimental part, p. 1085 - 1087 (2011/12/16)

Silica supported perchloric acid catalyzes efficiently the reaction of carbamates and oxazolidinones with anhydrides in the presence of silica sulfuric acid under solvent-free conditions. All the reactions were done at room temperature and the N-acyl carb

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