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IODOACETIC ANHYDRIDE

CAS No.
54907-61-8
Chemical Name:
IODOACETIC ANHYDRIDE
Synonyms
Iodoacetyl anhydride;IODOACETIC ANHYDRIDE;2-iodoacetic anhydride;iodoaceticanhydride90+%;Di(iodoacetic)anhydride;Iodoacetic anhydride,97%;Iodoacetic acid anhydride;Bis(iodoacetic acid)anhydride;Acetic acid, 2-iodo-, 1,1'-anhydride;IODOACETIC ANHYDRIDE ISO 9001:2015 REACH
CBNumber:
CB7769432
Molecular Formula:
C4H4I2O3
Molecular Weight:
353.88
MDL Number:
MFCD00001080
MOL File:
54907-61-8.mol
Last updated:2023-04-23 13:52:06

IODOACETIC ANHYDRIDE Properties

Melting point 47-49 °C (lit.)
Boiling point 276.9±25.0 °C(Predicted)
Density 2.664±0.06 g/cm3(Predicted)
Flash point >230 °F
storage temp. 2-8°C
solubility chloroform: soluble10%, clear to slightly hazy, yellow (pink or tan)
form Crystalline Powder
color Yellow
BRN 1812140

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictograms
GHS05,GHS06
Signal word  Danger
Hazard statements  H301-H314
Precautionary statements  P260-P270-P280-P303+P361+P353-P304+P340+P310-P305+P351+P338
Hazard Codes  T,C
Risk Statements  25-35
Safety Statements  22-36/37/39-45
RIDADR  UN 3261 8/PG 2
WGK Germany  3
8-10-21
HazardClass  8
PackingGroup  III
HS Code  29159000

IODOACETIC ANHYDRIDE price More Price(4)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 284262 Iodoacetic anhydride 54907-61-8 250mg $85.7 2024-03-01 Buy
Sigma-Aldrich 284262 Iodoacetic anhydride 54907-61-8 1g $257 2024-03-01 Buy
TRC I685615 IodoaceticAcidAnhydride 54907-61-8 25mg $65 2021-12-16 Buy
American Custom Chemicals Corporation HCH0067348 IODOACETIC ANHYDRIDE 95.00% 54907-61-8 1G $256.2 2021-12-16 Buy
Product number Packaging Price Buy
284262 250mg $85.7 Buy
284262 1g $257 Buy
I685615 25mg $65 Buy
HCH0067348 1G $256.2 Buy

IODOACETIC ANHYDRIDE Chemical Properties,Uses,Production

Chemical Properties

Golden flakes

Uses

Reagent used as linker for development of reagents used for differential protein quantitation via ion scanning

Reactant used for:

  • Sythesis of N-iodoacetyl glycosylamine derivatives and converting amino precursors to IA derivatives
  • Linking lysine residues to N-terminal α-amino groups of peptides
  • Capping amines and yielding a thiol reactive iodo-derivative
  • Iodoacetylation

64-69-7
38020-81-4
54907-61-8
Synthesis of IODOACETIC ANHYDRIDE from Iodoacetic acid

IODOACETIC ANHYDRIDE Preparation Products And Raw materials

IODOACETIC ANHYDRIDE Suppliers

Global( 41)Suppliers
Supplier Tel Email Country ProdList Advantage
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GIHI CHEMICALS CO.,LIMITED
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Aladdin Scientific
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Hebei Weibang Biotechnology Co., Ltd
+8615350571055 Sibel@weibangbio.com China 6087 58
SHANGHAI KEAN TECHNOLOGY CO., LTD.
+8613817748580 cooperation@kean-chem.com China 40066 58
J & K SCIENTIFIC LTD. 010-82848833 400-666-7788 jkinfo@jkchemical.com China 96815 76
Bis(iodoacetic acid)anhydride Di(iodoacetic)anhydride Iodoacetic acid anhydride Iodoacetic anhydride,97% 2-iodoacetic anhydride IODOACETIC ANHYDRIDE iodoaceticanhydride90+% Iodoacetyl anhydride Acetic acid, 2-iodo-, 1,1'-anhydride IODOACETIC ANHYDRIDE ISO 9001:2015 REACH 54907-61-8 C4H4I2O3 C4H4O3I2 ICH2CO2O Organic Building Blocks Carboxylic Acid Anhydrides Carbonyl Compounds Building Blocks Carbonyl Compounds Carboxylic Acid Anhydrides Organic Building Blocks