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19520-95-7

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19520-95-7 Usage

Derived from

acetic acid

Industrial uses

solvent, intermediate in organic synthesis, manufacture of pharmaceuticals and personal care products

Physical properties

clear, colorless liquid; mild odor; soluble in organic solvents like ethanol and acetone

Safety

relatively safe for use when handled properly

Storage

store in a cool, dry place away from sources of ignition and incompatible materials to prevent potential hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 19520-95-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,5,2 and 0 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 19520-95:
(7*1)+(6*9)+(5*5)+(4*2)+(3*0)+(2*9)+(1*5)=117
117 % 10 = 7
So 19520-95-7 is a valid CAS Registry Number.

19520-95-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[acetyl(butyl)amino]ethyl acetate

1.2 Other means of identification

Product number -
Other names Acetamide,N-[2-(acetyloxy)ethyl]-N-butyl

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:19520-95-7 SDS

19520-95-7Downstream Products

19520-95-7Relevant articles and documents

Acylated 1,3-aminopropanols as repellents against bloodsucking arthropods

Boeckh,Breer,Geier,Hoever,Kruger,Nentwig,Sass

, p. 359 - 373 (2007/10/03)

Starting from a set of known repellent compounds, a general structural framework with high probability for repellent activity was developed by molecular modelling techniques. Synthesis, structure-biological activity relationships of acylated 1,3-aminoprop

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