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Bis(2-hydroxyethyl) piperazine-1,4-dicarboxylate, commonly known as BHEP, is a chemical compound with the molecular formula C10H16N2O6. It is a white crystalline solid that is soluble in water and slightly soluble in ethanol. BHEP is a derivative of piperazine, a heterocyclic amine, and is formed by the reaction of piperazine-1,4-dicarboxylic acid with ethylene oxide. bis(2-hydroxyethyl) piperazine-1,4-dicarboxylate is primarily used as a chelating agent in various applications, including water treatment, detergents, and as a stabilizer in the pharmaceutical industry. Its ability to form stable complexes with metal ions makes it an effective component in preventing scale formation and corrosion in industrial processes.

7709-79-7

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7709-79-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7709-79-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,0 and 9 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7709-79:
(6*7)+(5*7)+(4*0)+(3*9)+(2*7)+(1*9)=127
127 % 10 = 7
So 7709-79-7 is a valid CAS Registry Number.

7709-79-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name bis(2-hydroxyethyl) piperazine-1,4-dicarboxylate

1.2 Other means of identification

Product number -
Other names -

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:7709-79-7 SDS

7709-79-7Relevant academic research and scientific papers

Aliphatic thermoplastic polyurethane-ureas and polyureas synthesized through a non-isocyanate route

Li, Suqing,Zhao, Jingbo,Zhang, Zhiyuan,Zhang, Junying,Yang, Wantai

, p. 6843 - 6852 (2015)

A simple non-isocyanate route for synthesizing aliphatic thermoplastic polyurethane-ureas (TPUUs) and thermoplastic polyureas (TPUreas) is presented. Melt transurethane polycondensation of isophorone diamine or diethylene glycol bis(3-aminopropyl) ether with bis(hydroxyethyl) hexanediurethane, bis(hydroxyethyl) isophoronediurethane or bis(hydroxyethyl) piperazinediurethane was conducted at 170?°C under a reduced pressure of 3 mmHg. A series of thermoplastic TPUUs and TPUreas were prepared, and were characterized by gel permeation chromatography, FT-IR, 1H-NMR, differential scanning calorimetry, thermogravimetric analysis, and tensile testing. The TPUUs and TPUreas have an Mn up to 14 900 g mol-1, an Mw up to 43 700 g mol-1, Tg between -18.6?°C and 116.8?°C, and an initial decomposition temperature of over 222.3?°C. A flexible TPUU exhibits a melting temperature of 77.7?°C, a tensile strength of 6.46 MPa, and an elongation at break of 180.20%.

PROCESS FOR PRODUCING URETHANE (METH)ACRYLATES AND NEW URETHANE (METH)ACRYLATES

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Page/Page column 23, (2008/06/13)

The invention relates to urethane(meth)acrylates and to a process for their production which comprises transesterification of hydroxyalkyl carbamates with an (meth)acrylate of formula [CH2=CR29-CO-O-]t-R30 wherein R29 is hydrogen or methyl, and R30 represents an alkyl, optionally substituted by hydroxy, which may contain from 1 to 10 ether bridges group, from 1 to 10 -CO- bridges and/or from 1 to 5 -O-CO- bridges, and at least one carbonate of formula (IX) and/or a diester of formula (X) wherein each R31,each R32,each R33,each R34is, independently, chosen from the group of alkyl and aryl, and R35 is alkylene, alkenylene or arylene.

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