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5297-17-6

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5297-17-6 Usage

Uses

{2-[(3-Carboxypropanoyl)oxy]ethyl}trimethylazanium Chloride can be used for neuromuscular blocking action of succinylmonocholine in the rat.

Check Digit Verification of cas no

The CAS Registry Mumber 5297-17-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,9 and 7 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5297-17:
(6*5)+(5*2)+(4*9)+(3*7)+(2*1)+(1*7)=106
106 % 10 = 6
So 5297-17-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H17NO4/c1-10(2,3)6-7-14-9(13)5-4-8(11)12/h4-7H2,1-3H3/p+1

5297-17-6 Well-known Company Product Price

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  • USP

  • (1623604)  Succinylmonocholine chloride  United States Pharmacopeia (USP) Reference Standard

  • 5297-17-6

  • 1623604-125MG

  • 14,578.20CNY

  • Detail

5297-17-6SDS

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 Bernsteinsaeuremonocholinchlorid

1.2 Other means of identification

Product number -
Other names [2-(3-carboxy-propionyloxy)-ethyl]-trimethyl-ammonium, chloride

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:5297-17-6 SDS

5297-17-6Downstream Products

5297-17-6Relevant articles and documents

Degradation properties and pH-responsive guest-release of cyclophanes having four ester side chains with terminal choline residues

Hayashida, Osamu,Sato, Daisuke

supporting information, p. 322 - 324 (2014/03/21)

Water-soluble cationic cyclophane 1 having four ester side chains with terminal choline residues was synthesized as a pH-responsive degradable host. Alkaline hydrolysis of the ester bonds of 1 gave the corresponding tetraanionic cyclophane 2, which exhibited guest-binding affinities that led to release of the entrapped anionic guest molecules into the bulk aqueous phase.

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