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70082-30-3

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70082-30-3 Usage

General Description

ISOBUTYL HYDRAZINE SULFATE is a chemical compound that is commonly used in pharmaceuticals, specifically in the synthesis of various medications. It is also used as a reagent in organic synthesis and as a propellant in the aerospace industry. The compound is a hydrazine derivative, which means it contains a nitrogen-nitrogen bond, and it is typically in the form of a white crystalline powder. ISOBUTYL HYDRAZINE SULFATE is considered hazardous and should be handled with care due to its toxic and potentially explosive properties. It is important to adhere to proper safety protocols when working with this chemical.

Check Digit Verification of cas no

The CAS Registry Mumber 70082-30-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,0,8 and 2 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 70082-30:
(7*7)+(6*0)+(5*0)+(4*8)+(3*2)+(2*3)+(1*0)=93
93 % 10 = 3
So 70082-30-3 is a valid CAS Registry Number.
InChI:InChI=1/C4H12N2/c1-4(2)3-6-5/h4,6H,3,5H2,1-2H3

70082-30-3SDS

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 2-methylpropylhydrazine,sulfuric acid

1.2 Other means of identification

Product number -
Other names i-butylhydrazine sulfate

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:70082-30-3 SDS

70082-30-3Relevant articles and documents

Practical approaches to the matrix metalloproteinase inhibitor Trocade (Ro 32-3555) and to the TNF-α converting enzyme inhibitor Ro 32-7315

Hilpert, Hans

, p. 7675 - 7683 (2007/10/03)

Stereoselective methods were found to efficiently prepare 2- and 3-substituted succinates with anti configuration. In the synthesis of Trocade 1, the hydantoinmethyl residue was introduced by alkylation of the non-chelated potassium enolate 19 with the br

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