Sodium iodoacetate

• Catalog No.: 57859
• CAS Number: 305-53-3
• M. F.: C2H2INaO2
• M. W.: 207.93032
• Purity: ≥99.0% (NT)

SYNONYMS

• IUPAC name: sodium 2-iodoacetate
• IUPAC Traditional name: sodium 2-iodoacetate
• Synonyms: Iodoacetic acid sodium salt; Iodoacetic acid 钠盐

DATABASE IDS

• Beilstein Number: 4009322
• EC Number: 206-165-7
• MDL Number: MFCD00002686
• CAS Number: 305-53-3

PROPERTIES

• Linear Formula: ICH2COONa
• Purity: ≥99.0% (NT)
• Melting Point: 208 °C (dec.)(lit.)
• GHS Signal Word: Danger
• GHS Hazard statements: H301-H315-H318-H335
• European Hazard Symbols: Toxic (T)
• Personal Protective Equipment: Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
• GHS Precautionary statements: P261-P280-P301 + P310-P305 + P351 + P338
• RID/ADR: UN 2811 6.1/PG 3
• Risk Statements: 25-37/38-41
• RTECS: AI3675000
• Safety Statements: 26-39-45
• Storage Temperature: -20°C
• Hazard Class: 6.1
• UN Number: 2811
• Packing Group: 3
• German water hazard class: 3

DETAILS

Description (English)

Caution
may discolor to yellowish on storage
Other Notes
Sulfhydryl reagent1,2
Application
Reagent for the modification of cysteine residues in proteins. Used in protein sequencing (including by Sanger in sequencing bovine insulin) to prevent oxidation of -SH sidechains.
Reagent for the modification of cysteine residues in proteins. Used to induce animal osteoarthritis model system, which mimics both symptoms and histopathology of the human disease.

Description (简体中文)

Caution
may discolor to yellowish on storage
Other Notes
Sulfhydryl reagent1,2
Application
Reagent for the modification of cysteine residues in proteins. Used in protein sequencing (including by Sanger in sequencing bovine insulin) to prevent oxidation of -SH sidechains.
Reagent for the modification of cysteine residues in proteins. Used to induce animal osteoarthritis model system, which mimics both symptoms and histopathology of the human disease.