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13952-69-7

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13952-69-7 Usage

General Description

1,2-di-tert-butylhydrazine is a chemical compound with the formula (CH3)3CNHNHC(CH3)3. It is a colorless, flammable liquid that is often used as a reagent in organic synthesis. 1,2-di-tert-butylhydrazine is also known for its use as a rocket fuel and in the rubber vulcanization process. It is important to handle this chemical with care as it is highly toxic and can cause severe irritation to the skin and eyes. Additionally, exposure to 1,2-di-tert-butylhydrazine has been linked to adverse health effects, including liver and kidney damage. Therefore, proper safety precautions and protective equipment must be used when working with this compound.

Check Digit Verification of cas no

The CAS Registry Mumber 13952-69-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,9,5 and 2 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 13952-69:
(7*1)+(6*3)+(5*9)+(4*5)+(3*2)+(2*6)+(1*9)=117
117 % 10 = 7
So 13952-69-7 is a valid CAS Registry Number.

13952-69-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-ditert-butylhydrazine

1.2 Other means of identification

Product number -
Other names 1,2-di-tert-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:13952-69-7 SDS

13952-69-7Relevant articles and documents

1-acylsemicarbazides by ring opening of iminodiaziridines with carboxylic acids: Novel, expeditious access to the azapeptide motif

Quast, Helmut,Schmitt, Edeltraud,Ross, Karl-Heinz

experimental part, p. 3358 - 3362 (2010/11/16)

Carboxylic acids react rapidly and quantitatively with iminodiaziridines to afford 1,2,4-trisubstituted 1-acylsemicarbazides in a multistep sequence. In this way, a carboxy group is readily converted into an azapeptide motif. Broad signals in high-field H and C NMR spectra recorded for the products are indicative of dynamic processes. Georg Thieme Verlag Stuttgart New York.

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