ChemicalBook >> CAS DataBase List >>Iodoacetic acid

Iodoacetic acid

CAS No.
64-69-7
Chemical Name:
Iodoacetic acid
Synonyms
IA;iodoacetate;monoiodoacetate;iodoacetic;lodoacetic acid;MONOIODOACETIC ACID;SKL245;CH2ICOOH;iodo-aceticaci;IODOACETIC ACID
CBNumber:
CB3854071
Molecular Formula:
C2H3IO2
Molecular Weight:
185.95
MDL Number:
MFCD00002685
MOL File:
64-69-7.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-05-28 04:19:11

Iodoacetic acid Properties

Melting point 79 °C
Boiling point 208°C
Density 2.2003 (estimate)
Flash point 208°C
storage temp. 2-8°C
solubility H2O: soluble, clear to hazy
form Liquid
pka 3.12(at 25℃)
color faintly yellow
biological source synthetic
Water Solubility 600 g/L (20 ºC)
Sensitive Light Sensitive
Merck 14,5025
BRN 1739079
Henry's Law Constant 2.4×102 mol/(m3Pa) at 25℃, HSDB (2015)
Stability Stable. Incompatible with strong oxidizing agents, bases, strong reducing agents. Store at -20 C.
InChI 1S/C2H3IO2/c3-1-2(4)5/h1H2,(H,4,5)
InChIKey JDNTWHVOXJZDSN-UHFFFAOYSA-N
SMILES OC(=O)CI
CAS DataBase Reference 64-69-7(CAS DataBase Reference)
EWG's Food Scores 1
FDA UNII WF5188V710
NIST Chemistry Reference Acetic acid, iodo-(64-69-7)
EPA Substance Registry System Iodoacetic acid (64-69-7)
UNSPSC Code 12352106
NACRES NA.77

SAFETY

Risk and Safety Statements

Symbol(GHS)  Corrosion (GHS05)Skull and Crossbones (GHS06)
GHS05,GHS06
Signal word  Danger
Hazard statements  H301-H314
Precautionary statements  P264-P270-P260-P280-P301+P310-P330-P301+P330+P331-P303+P361+P353-P363-P304+P340-P310-P305+P351+P338-P405-P501
PPE Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
Hazard Codes  T,C
Risk Statements  25-35
Safety Statements  22-36/37/39-45
RIDADR  UN 2923 8/PG 1
WGK Germany  1
RTECS  AI3500000
F  8-9
TSCA  TSCA listed
HazardClass  8
PackingGroup  II
HS Code  29159080
Storage Class 6.1A - Combustible acute toxic Cat. 1 and 2
very toxic hazardous materials
Hazard Classifications Acute Tox. 3 Oral
Eye Dam. 1
Skin Corr. 1A
Hazardous Substances Data 64-69-7(Hazardous Substances Data)
Toxicity LD50 intravenous in dog: 45mg/kg
NFPA 704
0
3 0

Iodoacetic acid price More Price(28)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich I4386 Iodoacetic acid ≥98.0% (T) 64-69-7 10g $63.3 2026-04-30 Buy
Sigma-Aldrich I4386 Iodoacetic acid ≥98.0% (T) 64-69-7 25g $118 2026-04-30 Buy
TRC TRC-I685520-50G Iodoacetic Acid 64-69-7 50g $674 2026-06-03 Buy
TRC TRC-I685520-1G Iodoacetic Acid 64-69-7 1g $178 2026-06-03 Buy
TRC TRC-I685520-10G Iodoacetic Acid 64-69-7 10g $376 2026-06-03 Buy
Product number Packaging Price Buy
I4386 10g $63.3 Buy
I4386 25g $118 Buy
TRC-I685520-50G 50g $674 Buy
TRC-I685520-1G 1g $178 Buy
TRC-I685520-10G 10g $376 Buy

Iodoacetic acid Chemical Properties, Uses, Production

Chemical Properties

white to light yellow crystalline powder

Uses

Used as a general reagent in acylation reactions. A byproduct formed in treated waters, and found in marine life.

Uses

Iodoacetic acid is used as a reagent for the modification of sulfhydryl groups in organic synthesis. It reacts with cysteine moiety in proteins to prevent the re-formation of disulfide bonds during protein sequencing. It is also used as a general reagent in acylation reactions as well as in glycopeptide synthesis.

Definition

ChEBI: A haloacetic acid that is acetic acid in which one of the hydrogens of the methyl group is replaced by an iodine atom.

General Description

Colorless or white crystals.

Air & Water Reactions

May be sensitive to heat, light, and air. Water soluble

Reactivity Profile

Iodoacetic acid reacts vigorously with bases and is corrosive.

Fire Hazard

Flash point data for Iodoacetic acid are not available, but Iodoacetic acid is probably non-flammable.

Biochem/physiol Actions

Iodoacetic acid (IAA) blocks the thiol group of cysteine. IAA inhibits glyceraldehyde-3-phosphate dehydrogenase (G3PDH) by interacting with sulfhydryl group of the active site cysteine. IAA inhibits the progression of solid Ehrlich carcinoma. IAA is one of the iodinated disinfection byproducts in drinking water. It is cytotoxic to mammalian cells.

Purification Methods

Crystallise it from pet ether (b 60-80o) or CHCl3/CCl4. [Beilstein 2 IV 534.]

Global Suppliers ( 183)
Supplier Tel Email Country ProdList Advantage
Nanjing Habo Medical Technology Co., Ltd. 13376080562 13376090521 sales@habotech.com China 727 60
Shandong Mingde Biotechnology Co., Ltd 15553348166 m15553348166@163.com China 2027 58
Meryer (Shanghai) Chemical Technology Co., Ltd. 4006356688 18621169109 market03@meryer.com China 40202 62
Alfa Aesar 400-6106006 saleschina@alfa-asia.com China 30103 84
Energy Chemical 400-0056266 sales8178@energy-chemical.com China 45000 61
Shanghai Hanhong Scientific Co.,Ltd. 021-54306202 13764082696 info@hanhongsci.com China 42917 64
Shandong Xiya Chemical Co., Ltd 13355009207 13355009207 3007715519@qq.com China 18722 57
Syntechem Co.,Ltd info@syntechem.com China 12973 57
Sichuan Kulinan Technology Co., Ltd 400-1166-196 18981987031 cdhxsj@163.com China 11674 57
China Langchem Inc. 0086-21-58956006 China 7798 57

View Latest Price from Iodoacetic acid manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Iodoacetic acid pictures 2026-09-02 Iodoacetic acid
64-69-7
20kg 99% 20 tons Qingdao RENAS Polymer Material Co., Ltd.
Iodoacetic acid pictures 2026-03-20 Iodoacetic acid
64-69-7
$1.00 1kg 99% 10 mt Hebei Chuanghai Biotechnology Co., Ltd
iodoacetic iodo-aceticaci Kyselina jodoctova kyselinajodoctova monoiodoacetate RARECHEM AL BO 0101 MONOIODOACETIC ACID VITAS-BB TBB000669 Aceticacid,iodo- CH2ICOOH IODOACETIC ACID MONO IODOACETIC ACID IODOACETIC ACID FREE ACID APPROX 99%,*YE LLOW POWDER IODOACETIC ACID APPROX. 99% WHITE TO OFF IODOACETIC ACID R. G. IodoaceticAcid>99% IodoaceticAcid97% IODOACETICACID,REAGENT Iodoethanoic acid Iodoacetic acid, 97% 25GR Iodoacetic acid, >=99.5% Iodiacetic acid IODOACETIC ACID, >= 98.0 % (T) Acetic acid, 2-iodo- lodoacetic acid SKL245 Iodoacetic acid, GR 99% IA iodoacetate 64-69-7 ICH2COOH ICH2CO2H C2H3IO2 Synthetic Reagents Organic Building Blocks Organic Acids Puriss p.a. General Use Building Blocks Analytical Reagents Analytical Chromatography Product Catalog C1 to C5 Carboxylic Acids Carbonyl Compounds Reagents for cysteine modification Specific Amino Acid Modification Protein Modification Analytical Reagents for General Use I-N, Puriss p.a. Puriss p.a. Chemical Synthesis Organic Acids Synthetic Reagents K00001