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53727-52-9

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53727-52-9 Usage

Chemical compound

1,4-bis[2-(1-piperazinyl)-ethyl]-Piperazine

Family

Piperazine

Structure

Contains two piperazine rings connected by an ethyl chain

Usage

Crosslinking agent in polyurethane polymers

Applications

a. Curing agent for epoxy resins
b. Crosslinking agent for polyurethane adhesives
c. Hardener for coatings

Benefits

Improves mechanical and thermal properties of polymers

Caution

Potential toxicity and reactivity, should be handled with care

Check Digit Verification of cas no

The CAS Registry Mumber 53727-52-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,7,2 and 7 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 53727-52:
(7*5)+(6*3)+(5*7)+(4*2)+(3*7)+(2*5)+(1*2)=129
129 % 10 = 9
So 53727-52-9 is a valid CAS Registry Number.

53727-52-9SDS

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 1,4-bis(2-piperazin-1-ylethyl)piperazine

1.2 Other means of identification

Product number -
Other names Piperazine,1,4-bis[2-(1-piperazinyl)ethyl]

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:53727-52-9 SDS

53727-52-9Downstream Products

53727-52-9Relevant articles and documents

PROCESS FOR MANUFACTURING ALKYLENEAMINE COMPOUNDS

-

Paragraph 0118-0121, (2021/09/11)

The invention pertains to a process for manufacturing alkyleneamine compounds, comprising the steps of - in a reaction medium reacting an alkyleneurea compound comprising at least one primary amine group, or at least one cyclic secondary amine group, or at least one primary amine group and at least one cyclic secondary amine group, and at least one cyclic alkyleneurea group of formula I wherein A is selected from the group of C2 to C4 alkylene units, optionally substituted by one or more C1 to C3 alkyl groups, with an alkylhalide compound to form an alkyleneamine hydrohalide salt comprising at least one cyclic alkyleneurea group of formula I, the alkylhalide compound being selected from the group of haloalkanes with 2-6 halogen atoms, and haloaminoalkanes, and - reacting the alkyleneamine hydrohalide salt with a base to form an alkyleneamine compound comprising at least one cyclic alkyleneurea group of formula I. In one embodiment the reaction is carried out in the presence of one or more of ammonia and additional alkyleneamine compound. The process according to the invention produces less cyclic and branched side products and more straight-chain higher alkyleneamines than conventional processes, in particular more straight-chain ethyleneamines selected from L-TETA, L-TEPA, and L-PEHA. The formula I is represented herein.

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