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137076-50-7

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  • 1,4,7,10-Tetrakis(ethoxycarbonylmethyl)-1,4,7,10-tetraazacyclododecane

    Cas No: 137076-50-7

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137076-50-7 Usage

General Description

1,4,7,10-Tetrakis(ethoxycarbonylmethyl)-1,4,7,10-tetraazacyclododecane, also known as TEC cyclen, is a chemical compound used in various applications including medicine and industry. It belongs to the family of macrocyclic compounds and is commonly used as a chelating agent to bind and remove metal ions from solutions. TEC cyclen has a high affinity for certain metals such as copper and can be used in the treatment of heavy metal poisoning. In addition, it is also used in the synthesis of radioactive metal chelates for imaging and diagnostic purposes in medicine. The compound's chemical structure allows for strong coordination with metal ions, making it a versatile and useful chemical in a variety of fields.

Check Digit Verification of cas no

The CAS Registry Mumber 137076-50-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,0,7 and 6 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 137076-50:
(8*1)+(7*3)+(6*7)+(5*0)+(4*7)+(3*6)+(2*5)+(1*0)=127
127 % 10 = 7
So 137076-50-7 is a valid CAS Registry Number.
InChI:InChI=1/C24H44N4O8/c1-5-33-21(29)17-25-9-11-26(18-22(30)34-6-2)13-15-28(20-24(32)36-8-4)16-14-27(12-10-25)19-23(31)35-7-3/h5-20H2,1-4H3

137076-50-7 Well-known Company Product Price

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  • Alfa Aesar

  • (H26646)  1,4,7,10-Tetrakis(ethoxycarbonylmethyl)-1,4,7,10-tetraazacyclododecane   

  • 137076-50-7

  • 250mg

  • 958.0CNY

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137076-50-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4,7,10-Tetrakis(ethoxycarbonylmethyl)-1,4,7,10-tetraazacyclododecane

1.2 Other means of identification

Product number -
Other names ethyl 2-[4,7,10-tris(2-ethoxy-2-oxoethyl)-1,4,7,10-tetrazacyclododec-1-yl]acetate

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:137076-50-7 SDS

137076-50-7Relevant articles and documents

Compositions for protecting skin

-

Paragraph 0142-0144, (2018/05/29)

The purpose of the present invention is to provide a skin outer layer composition which does not have or has very low skin irritation or toxicity, and has a high ability to remove formaldehyde and heavy metals compared to conventional material. The present invention provides the skin outer layer composition comprising, as active ingredients, one or more selected from trientine or trientine derivatives represented by chemical formula 1, cyclen or cyclen derivatives represented by chemical formula 2, and cyclam or cyclam derivatives represented by chemical formula 3. In the above formulas, R_1, R_2, R_3, R_4, R_5 and R_6 are each independently hydrogen, -R_7-COOH or salts thereof, and R_7 is a C_1-C_5 aliphatic group, a substituted or unsubstituted aromatic group, or a heterocyclic six-membered or five-membered ring.COPYRIGHT KIPO 2018

A convenient, novel approach for the synthesis of polyaza macrocyclic bifunctional chelating agents

Mishra, Anil Kumar,Draillard, Karine,Faivre-Chauvet, Alain,Gestin, Jean Francois,Curtet, Chantal,Chatal, Jean-Francois

, p. 7515 - 7518 (2007/10/03)

The convenient synthetically useful bifunctional chelating agents, (10-p-aminobenzyl)-1,4,7,10-tetraazacyclododecane-1,4,7-triacetate (p-ABz-DO3A) 3 and (11-p-aminobenzyl)-1,4,8,11-tetraazacyclotetradecane-1,4,8-triacetate (p-ABz-TE3A) 6, were obtained by reaction of an ethyl bromoacetate with 1,4,7,10-tetraazacyclododecane and 1,4,8,11-tetraazacyclotetradecane followed by reaction with nitrobenzyl bromide. This method proved more efficient than any described in the literature since the overall yield in a two-step synthesis sequence starting from tetraazamacrocycles was 68%.

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