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1,2-Propanediamine, N,N'-dibutyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

37480-97-0

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37480-97-0 Usage

Physical appearance

Clear, colorless liquid

Odor

Faint amine odor

Solubility

Soluble in water

Uses

Cross-linking agent in industrial applications (e.g. adhesives, sealants, coatings), manufacture of polymers and resins, corrosion inhibitor in metal processing

Safety precautions

Can cause skin and eye irritation, may be harmful if ingested or inhaled, proper safety measures and protective equipment should be used.

Check Digit Verification of cas no

The CAS Registry Mumber 37480-97-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,4,8 and 0 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 37480-97:
(7*3)+(6*7)+(5*4)+(4*8)+(3*0)+(2*9)+(1*7)=140
140 % 10 = 0
So 37480-97-0 is a valid CAS Registry Number.

37480-97-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-N,2-N-dibutylpropane-1,2-diamine

1.2 Other means of identification

Product number -
Other names N,N'-Dibutyl-1-methyl-aethandiyldiamin

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:37480-97-0 SDS

37480-97-0Downstream Products

37480-97-0Relevant academic research and scientific papers

PROCESS FOR PREPARING A 1,2-ETHYLENEDIAMINE OR 1,2-PROPYLENEDIAMINE

-

Page/Page column 5-6, (2011/05/03)

The present invention generally relates to a process for preparing a 1,2-ethylenediamine; 1,2-propylenediamine; or a mixture thereof by way of a catalyzed reductive amination reaction employing hydrogen, a reductive amination catalyst, (C3-C40)polyhydric alcohol having at least three hydroxy groups on consecutive carbon atoms thereof, and primary amine, the catalyzed reductive amination reaction employing reaction conditions that are effective for reductively aminating at least two of the hydroxy groups of the (C3-C40)polyhydric alcohol and reductively eliminating at least one other of the hydroxy groups of the (C3-C40)polyhydric alcohol in such a way so as to give a 1,2-ethylenediamine; 1,2-propylenediamine; or a mixture thereof.

Polyfunctionalized N-Tensides. VII. Substitution and Elimination in the Reaction of 1,2-Dihalogenoalkanes with Amines

Beger, J.,Meerbote, E.

, p. 12 - 22 (2007/10/02)

1,2-Dichloroalkanes, 1,2-Dibromoalkanes and mixtures of 1-bromo-2-chloroalkanes and 1-chloro-2-bromoalkanes react with primary or secondary amines and give both elimination and substitution products, often in a nearly 1:1 proportion.The elimination products are the cis and trans-1-halo-1-alkenes, the 2-halo-1-alkenes, the 1,3- and 2,4-dienes and the 1-alkenes.The main substitution products are the 1,2-bis-aminoalkanes.Physical dates, 1H-n.m.r.-spectra,surface tension values and CMC-dates are given.

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