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2-Iodoacetamide, 98%, stab. with ca 5-8% water
CAS: 144-48-9 | C2H4INO | 184.964 g/mol
$60.38 - $533.12
Chemical Identifiers
| CAS | 144-48-9 |
|---|---|
| Molecular Formula | C2H4INO |
| Molecular Weight (g/mol) | 184.964 |
| MDL Number | MFCD00008028 |
| InChI Key | PGLTVOMIXTUURA-UHFFFAOYSA-N |
| Synonym | iodoacetamide, monoiodoacetamide, surauto, acetamide, 2-iodo, 2-iodo-acetamide, usaf d-1, alpha-iodoacetamide, ccris 7710, unii-zrh8m27s79, n-3-methoxy-4-butoxybenzyl thiobarbituric acid |
| PubChem CID | 3727 |
| IUPAC Name | 2-iodoacetamide |
| SMILES | C(C(=O)N)I |
| Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
|---|---|---|---|---|---|---|---|---|---|
| Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
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AAA1471506
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Thermo Scientific Chemicals
A1471506 |
5 g |
Each for $60.38
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AAA1471514
|
Thermo Scientific Chemicals
A1471514 |
25 g |
Each for $167.53
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AAA1471522
|
Thermo Scientific Chemicals
A1471522 |
100 g |
Each for $533.12
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Description
Alkylating agent used in peptide mapping because it covalently binds with the thiols in cysteine to prevent disulfide bond formation2-Iodoacetamide is used as an electrophile for covalent modification of nucleophilic residues on proteins such as cysteine, methionine and histidine. It is used to bind with thiol group of cysteine, thereby it protects the formation disulfide bonds. It is involved as an inhibitor of deubiquitinase enzymes (DUBs). Further, it acts as an alkylating sulfhydryl reagent.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
ApplicationsAlkylating agent used in peptide mapping because it covalently binds with the thiols in cysteine to prevent disulfide bond formation2-Iodoacetamide is used as an electrophile for covalent modification of nucleophilic residues on proteins such as cysteine, methionine and histidine. It is used to bind with thiol group of cysteine, thereby it protects the formation disulfide bonds. It is involved as an inhibitor of deubiquitinase enzymes (DUBs). Further, it acts as an alkylating sulfhydryl reagent.
Solubility
Soluble in water, dimethyl formamide and ethanol. Slightly soluble in methanol.
Notes
Store in a cool place. Light and moisture sensitive. Keep the container tightly closed in a dry and well-ventilated place. Incompatible with strong acids, strong bases, strong oxidizing agents and strong reducing agents.
Chemical Identifiers
| 144-48-9 | |
| 184.964 | |
| PGLTVOMIXTUURA-UHFFFAOYSA-N | |
| 3727 | |
| C(C(=O)N)I |
| C2H4INO | |
| MFCD00008028 | |
| iodoacetamide, monoiodoacetamide, surauto, acetamide, 2-iodo, 2-iodo-acetamide, usaf d-1, alpha-iodoacetamide, ccris 7710, unii-zrh8m27s79, n-3-methoxy-4-butoxybenzyl thiobarbituric acid | |
| 2-iodoacetamide |
Specifications
| 144-48-9 | |
| 98%, stabilized with ca 5% water | |
| MFCD00008028 | |
| UN2811 | |
| Light sensitive | |
| Soluble in water,dimethyl formamide and ethanol. Slightly soluble in methanol. | |
| C(C(=O)N)I | |
| 184.964 | |
| 184.96 | |
| Iodoacetamide, stabilized with ≈5 to 8% water |
| 92°C to 95°(dried) | |
| C2H4INO | |
| 5 g | |
| 1739080 | |
| iodoacetamide, monoiodoacetamide, surauto, acetamide, 2-iodo, 2-iodo-acetamide, usaf d-1, alpha-iodoacetamide, ccris 7710, unii-zrh8m27s79, n-3-methoxy-4-butoxybenzyl thiobarbituric acid | |
| PGLTVOMIXTUURA-UHFFFAOYSA-N | |
| 2-iodoacetamide | |
| 3727 | |
| 98% |
Safety and Handling
GHS H Statement
H301-H315-H319-H317-H335
P260-P264b-P270-P271-P272-P280-P285-P303+P361+P353-P304+P340-P305+P351+P338-P310-P330-P331-P333+P313-P363-P501c
H301-H314-H317-H334-H335
DOTInformation : Transport Hazard Class: 6.1; Packing Group: III; Proper Shipping Name: TOXIC SOLIDS, ORGANIC, N.O.S.
EINECSNumber : 205-630-1
RTECSNumber : AC4200000
TSCA : Yes
Recommended Storage : Keep cold
RUO – Research Use Only