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Iodoacetic acid potassium salt is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

15973-59-8

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15973-59-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15973-59-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,9,7 and 3 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 15973-59:
(7*1)+(6*5)+(5*9)+(4*7)+(3*3)+(2*5)+(1*9)=138
138 % 10 = 8
So 15973-59-8 is a valid CAS Registry Number.
InChI:InChI=1/C2H3IO2.K/c3-1-2(4)5;/h1H2,(H,4,5);/q;+1/p-1

15973-59-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name potassium,2-iodoacetate

1.2 Other means of identification

Product number -
Other names Acetic acid,2-iodo-,potassium salt (1:1)

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:15973-59-8 SDS

15973-59-8Relevant academic research and scientific papers

The thermally solid-state in reaction in halogenoacetates

Epple, Matthias,Kirschnick, Holger

, p. 1123 - 1129 (1996)

Nine salts of halogenoacetic acids MOOC-CH2-X were prepared and characterized by their thermochemical reactivity. It was found that in seven cases elimination of MX led to polymerization of the organic part of the molecule. The resulting polyester, polyglycolide, could be isolated easily by washing the reaction product with water. It has a distinct porous morphology. The reaction takes place at moderate temperatures (100-200 °C). VCH Verlagsgesellschaft mbH, 1996.

Reactions of nucleophilic substitution involving solid organic halogen compounds under shear deformation at high pressure

Zharov, A. A.,Chistotina, N. P.,Gaziev, R. G.,Yakovleva, I. I.

, p. 1050 - 1055 (2007/10/02)

Under conditions of shear deformation and high pressures (SD + HP), reactions of nucleophilic substitution were studied: 1) the replacement of aliphatic halogen atom with alkaline metal halides (halo-substituted aliphatic carboxylic acids, 1-bromoadamantane); 2) the replacement of halogen atom in aromatic nucleus (halobenzoic acids, dihalobenzenes) with halogen of salt; 3) the replacement of aliphatic halogen with hydroxyl (hydrolysis in a solid phase); 4) the replacement of halogen with amino group under deformation of the samples of ammonium α-halocarboxylates to give the corresponding amino acids.It was found that the exchange of the halogen atoms bonded with aliphatic carbon is most intensive in the mixtures of alkaline metal iodides with bromo-substituted acetic acid and propionic acids: the exchange reaction in these mixtures is observed even during grinding in the mortar. Unlike the liquid phase, under conditions of SD + HP exchange of the halogen atom of the aromatic nucleus with alkaline metal halides, proceeds successfully, and the reactivity of halides increases in the series Na K Rb Cs.Under SD + HP, 1-Br-adamantane reacts with water to form 1-adamantanol.A high reactivity of the water adsorbed by the reagents is observed. - Key words: shear deformation, high pressure, halogen derivatives of carboxylic acids, dihalobenzenes, alkaline metal halides, ammonium salts of halogen derivatives of carboxylic acids, amino acids, halo-substituted adamantanes, adamantanol, nucleophilic substitution reaction, hydrolysis, ball mill.

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