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36555-73-4

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36555-73-4 Usage

Chemical structure

A 15-carbon chain with an amine group at one end and two ethyl groups attached to the nitrogen atom.

Usage

Commonly used as an intermediate in the synthesis of various pharmaceuticals, organic compounds, and surfactants.

Applications

Utilized as a corrosion inhibitor, an anti-foaming agent, and a lubricant additive.

Physical properties

Known for its strong odor.

Safety precautions

Potential to cause skin and eye irritation; should be handled with care.

Environmental concerns

May pose environmental hazards and should be properly disposed of according to local regulations.

Check Digit Verification of cas no

The CAS Registry Mumber 36555-73-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,5,5 and 5 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 36555-73:
(7*3)+(6*6)+(5*5)+(4*5)+(3*5)+(2*7)+(1*3)=134
134 % 10 = 4
So 36555-73-4 is a valid CAS Registry Number.

36555-73-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N-diethylpentadecan-1-amine

1.2 Other means of identification

Product number -
Other names Diaethyl-pentadecyl-amin

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:36555-73-4 SDS

36555-73-4Downstream Products

36555-73-4Relevant articles and documents

Joint Synthesis of Tertiary Unsymmetrical and Symmetrical Aliphatic Amines

Kozlov,Tereshko,Basalaeva,Tarasevich

, p. 1095 - 1098 (2007/10/03)

Tertiary unsymmetrical and symmetrical aliphatic amines were prepared by reaction of higher (C8-C16) and lower (C2-C4) aliphatic alcohols with nitriles containing the same number of carbon atoms as the lower aliphatic alcohols. Reaction conditions ensuring nearly quantitative yields of tertiary amines were determined.

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