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1744-71-4

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1744-71-4 Usage

Physical state

Colorless liquid

Odor

Slightly unpleasant

Solubility

Soluble in most organic solvents

Uses

a. Reagent in organic synthesis
b. Pharmaceutical intermediate

Health hazards

a. Potential carcinogen
b. Mutagen
c. Causes irritation to eyes, skin, and respiratory system

Environmental concerns

Identified as a possible environmental contaminant

Handling and disposal

Requires careful handling and proper disposal to prevent harm to human health and the environment

Check Digit Verification of cas no

The CAS Registry Mumber 1744-71-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,4 and 4 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1744-71:
(6*1)+(5*7)+(4*4)+(3*4)+(2*7)+(1*1)=84
84 % 10 = 4
So 1744-71-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H20N2.2ClH/c1-3-5-7-9-10-8-6-4-2;;/h9-10H,3-8H2,1-2H3;2*1H

1744-71-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-dibutylhydrazine

1.2 Other means of identification

Product number -
Other names 1,2-Di-n-butylhydrazine

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:1744-71-4 SDS

1744-71-4Relevant articles and documents

The Heat of Oxidation of 1,2-Di-n-butylhydrazine to Azo-n-butane

Engel, Paul S.,Owens, Walter H.,Wang, Chengrong

, p. 10486 - 10488 (1993)

1,2-di-n-butylhydrazine in hexane solution has been oxidized to azo-n-butane with oxygen and Pd/C catalyst and with red mercuric oxide.Both methods led to the same calculated heat of hydrogenation (ΔHH) of the azo group in hexane, -16.4 +/- 0.3 kcal/mol.This value is 10.6 kcal/mol less exothermic than the ΔHH of carbon-carbon double bonds.

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