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Iodoacetic anhydride_Molecular_structure_CAS_54907-61-8)
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Iodoacetic anhydride

Catalog No. 284262 Name Sigma Aldrich
CAS Number 54907-61-8 Website http://www.sigmaaldrich.com
M. F. C4H4I2O3 Telephone 1-800-521-8956
M. W. 353.8817 Fax
Purity Email
Storage Chembase ID: 148685

SYNONYMS

Title
碘代乙酸酐
IUPAC name
2-iodoacetyl 2-iodoacetate
IUPAC Traditional name
2-iodoacetyl 2-iodoacetate

DATABASE IDS

PubChem SID 24857144
CAS Number 54907-61-8
Beilstein Number 1812140
MDL Number MFCD00001080

PROPERTIES

Linear Formula (ICH2CO)2O
Flash Point 110 °C
Flash Point 230 °F
Melting Point 47-49 °C(lit.)
GHS Pictograms GHS05
GHS Pictograms GHS06
GHS Signal Word Danger
GHS Hazard statements H301-H314
European Hazard Symbols Toxic Toxic (T)
European Hazard Symbols Corrosive Corrosive (C)
MSDS Link Download
Personal Protective Equipment Eyeshields, Faceshields, full-face particle respirator type N100 (US), Gloves, respirator cartridge type N100 (US), type P1 (EN143) respirator filter, type P2 (EN 143) respirator cartridges, type P3 (EN 143) respirator cartridges
GHS Precautionary statements P280-P305 + P351 + P338-P310
RID/ADR UN 3261 8/PG 2
Risk Statements 25-35
Safety Statements 22-36/37/39-45
Storage Temperature 2-8°C
Hazard Class 8
UN Number 3261
Packing Group 2
German water hazard class 3

DETAILS

Description (English)
Packaging
1 g in glass bottle
250 mg in glass bottle
Application
Reagent used as linker for development of reagents used for differential protein quantitation via ion scanning1Reactant used for:
• Sythesis of N-iodoacetyl glycosylamine derivatives2 and converting amino precursors to IA derivatives3
• Linking lysine residues to N-terminal α-amino groups of peptides4
• Capping amines and yielding a thiol reactive iodo-derivative5
• Iodoacetylation6
Description (简体中文)
包装
1 g in glass bottle
250 mg in glass bottle
Application
Reagent used as linker for development of reagents used for differential protein quantitation via ion scanning1Reactant used for:
• Sythesis of N-iodoacetyl glycosylamine derivatives2 and converting amino precursors to IA derivatives3
• Linking lysine residues to N-terminal α-amino groups of peptides4
• Capping amines and yielding a thiol reactive iodo-derivative5
• Iodoacetylation6

REFERENCES