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106-59-2

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106-59-2 Usage

General Description

1,4-Piperazinediamine, also known as putrescine, is a chemical compound with the formula C4H12N2. It is a diamine that is commonly used in the production of polyurea coatings, adhesives, and elastomers. The compound is a colorless liquid that is soluble in water, and it has a faint odor. 1,4-Piperazinediamine is a key building block for the production of a wide range of industrial and consumer products, including pharmaceuticals, agrochemicals, and personal care items. Additionally, it has applications in the food industry as a potential food additive and preservative. However, it is important to handle this chemical with caution as it can be corrosive to the skin, eyes, and respiratory system if not properly managed.

Check Digit Verification of cas no

The CAS Registry Mumber 106-59-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,0 and 6 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 106-59:
(5*1)+(4*0)+(3*6)+(2*5)+(1*9)=42
42 % 10 = 2
So 106-59-2 is a valid CAS Registry Number.
InChI:InChI=1/C4H12N4/c5-7-1-2-8(6)4-3-7/h1-6H2

106-59-2SDS

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 piperazine-1,4-diamine

1.2 Other means of identification

Product number -
Other names Piperazine,4-diamino

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:106-59-2 SDS

106-59-2Upstream product

106-59-2Downstream Products

106-59-2Relevant articles and documents

Synthesis of a 4-aza analog of phencarol and its pharmacological investigation

Yakhontov,Kutina,Shishkin,Zhikhareva,Vysochin,Vorob'eva,Kaminka,Shevchenko,Mashkovskii

, p. 24 - 30 (2007/10/02)

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