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2-Iodoacetamide

Product Name
2-Iodoacetamide
CAS No.
144-48-9
Chemical Name
2-Iodoacetamide
Synonyms
IODOACETAMIDE;IAM;IODACETAMIDE;Surauto;usafd-1;USAF d-1;2-Iodacetamid;Iodoethanamide;2-iodo-acetamid;2-IODOACETAMIDE
CBNumber
CB4760867
Molecular Formula
C2H4INO
Formula Weight
184.96
MOL File
144-48-9.mol
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2-Iodoacetamide Property

Melting point:
92-95 °C(lit.)
Boiling point:
297.1±23.0 °C(Predicted)
Density 
2.1103 (estimate)
storage temp. 
2-8°C
solubility 
Soluble in water, dimethyl formamide and ethanol. Slightly soluble in methanol.
form 
crystalline
pka
15.16±0.40(Predicted)
color 
White to pale yellow or beige
Water Solubility 
H2O: 0.5M at 20°C, clear, colorless
Sensitive 
Light Sensitive
BRN 
1739080
Stability:
Stable, but light sensitive. Incompatible with strong oxidizing agents, strong bases, reducing agents, acids.
InChIKey
PGLTVOMIXTUURA-UHFFFAOYSA-N
CAS DataBase Reference
144-48-9(CAS DataBase Reference)
NIST Chemistry Reference
Alpha-iodo acetamide(144-48-9)
EPA Substance Registry System
2-Iodoacetamide (144-48-9)
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Safety

Hazard Codes 
T
Risk Statements 
25-42/43-43-36/37/38-53
Safety Statements 
22-36/37-45-37/39-26-24
RIDADR 
UN 2811 6.1/PG 3
WGK Germany 
3
RTECS 
AC4200000
8-10-21
TSCA 
T
HazardClass 
6.1
PackingGroup 
III
HS Code 
29241900
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H301Toxic if swalloed

H317May cause an allergic skin reaction

H334May cause allergy or asthma symptoms or breathing difficulties if inhaled

H413May cause long lasting harmful effects to aquatic life

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P273Avoid release to the environment.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P301+P310IF SWALLOWED: Immediately call a POISON CENTER or doctor/physician.

P302+P352IF ON SKIN: wash with plenty of soap and water.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
8.04744
Product name
2-Iodoacetamide
Purity
for synthesis
Packaging
25g
Price
$73.2
Updated
2024/03/01
Sigma-Aldrich
Product number
8.04744
Product name
2-Iodoacetamide
Purity
for synthesis
Packaging
100g
Price
$233
Updated
2024/03/01
Sigma-Aldrich
Product number
A3221
Product name
Iodoacetamide
Purity
Single use vial of 56 mg
Packaging
10vials
Price
$97.9
Updated
2024/03/01
Sigma-Aldrich
Product number
8.04744
Product name
2-Iodoacetamide
Purity
for synthesis
Packaging
1kg
Price
$1500
Updated
2024/03/01
Sigma-Aldrich
Product number
8.04744
Product name
2-Iodoacetamide
Purity
for synthesis
Packaging
2.5kg
Price
$3550
Updated
2024/03/01
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2-Iodoacetamide Chemical Properties,Usage,Production

Chemical Properties

White solid in amber, foil sealed microtubes. Soluble in hot water, easily soluble in ethanol.

Uses

2-Iodoacetamide is an alkylating reagent for cysteine residues in peptide sequencing. Its actions are similar to those of iodoacetate. By virtue of reaction with cysteine, it is an irreversible inhibitor of enzymes with cysteine at the active site. It reacts much more slowly with histidine residues, but that activity is responsible for inhibition of ribonuclease.

Application

Alkylating agent used in peptide mapping because it covalently binds with the thiols in cysteine to prevent disulfide bond formation 2-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.

Synthesis

2-Iodoacetamide is synthesized by reacting chloroacetamide with sodium iodide. The chloroacetamide, anhydrous acetone, and anhydrous sodium iodide were refluxed on the bath for 15h. Cool to room temperature, filter out sodium chloride, recover acetone, pour into ice water of sodium bisulfate after a little cooling, and then neutralize to pH 6 with saturated sodium sulfate solution. Cool to crystallize and filter to obtain crude product. The crude product is recrystallized with water to obtain the finished product.

Purification Methods

Crystallise it from water or CCl4. It is used for tagging proteins. [Gurd Methods Enzymol 25 424 1972, Beilstein 2 IV 536.]

Preparation and handling

Alkylation Procedure
Iodoacetamide is unstable and light-sensitive. Prepare solutions immediately before use and perform alkylation in the dark. If iodoacetamide is present in limiting quantities and a slightly alkaline pH, cysteine modification will be the exclusive reaction. Excess iodoacetamide or non-buffered iodoacetamide reagent can also alkylate amines (lysine, N-termini), thioethers (methionine), imidazoles (histidine) and carboxylates (aspartate, glutamate).
1. Add 5 μl of 2% SDS and 45 μl of 200 mM ammonium bicarbonate (pH 8.0) to 20-100 μg of protein sample. Adjust volume to 100 μl with ultrapure water.
2. Add 5 μl of 200 mM Tris(2-carboxyethyl) phosphine hydrochloride (TCEP.HCl, Product No. 20490) and incubate sample at 55°C for 1 hour.
3. Immediately before use, dissolve one tube of iodoacetamide (9.3 mg) with 132 μl of 200 mM ammonium bicarbonate (pH 8.0) to make 375 mM iodoacetamide. Protect solution from light.
4. Add 5 μl of the 375 mM iodoacetamide to the sample and incubate for 30 minutes protected from light.
5. Proceed to proteolytic digestion before MS analysis or other processing.

Precautions

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.

2-Iodoacetamide Preparation Products And Raw materials

Raw materials

Preparation Products

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2-Iodoacetamide Suppliers

Taizhou Chemedir Biopharm-tech. Co., Ltd
Tel
0523-86200218 18994667082
Fax
+86 523-86200613
Email
sale1_cmd@chemedir.com
Country
China
ProdList
110
Advantage
64
Creasyn Finechem(Tianjin) Co., Ltd.
Tel
022-022-83946278 13820372920
Fax
022-83945176
Email
sales@creasyn.com
Country
China
ProdList
1002
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68
Hunan Zhangjiajie Hengkang Biological Pharmaceutical Co., LTD
Tel
0731-85561023 18973109536
Email
hengkangapi@hengkangapi.com
Country
China
ProdList
429
Advantage
58
Xiamen Yunfan Biotech Co., Ltd.
Tel
0592-7828678 18050056030
Fax
0592-7828678
Email
yezhaobao@yfpharm.com
Country
China
ProdList
63
Advantage
58
Hunan Hui Bai Shi Biotechnology Co., Ltd.
Tel
0731-85526065 13308475853
Email
ivy@hnhbsj.com
Country
China
ProdList
4548
Advantage
62
J & K SCIENTIFIC LTD.
Tel
010-82848833 400-666-7788
Fax
86-10-82849933
Email
jkinfo@jkchemical.com
Country
China
ProdList
94838
Advantage
76
Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
4006608290; 18621169109
Fax
86-21-61259102
Email
market03@meryer.com
Country
China
ProdList
40241
Advantage
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Beijing Donghualituo Techonlogy Development Co.,Ltd.
Tel
010-88425576
Fax
(+86)-10-88425546
Email
sales@dhltchem.com
Country
China
ProdList
793
Advantage
59
Alfa Aesar
Tel
400-6106006
Fax
021-67582001/03/05
Email
saleschina@alfa-asia.com
Country
China
ProdList
30132
Advantage
84
TCI (Shanghai) Development Co., Ltd.
Tel
021-67121386
Fax
021-67121385
Email
Sales-CN@TCIchemicals.com
Country
China
ProdList
24539
Advantage
81
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View Lastest Price from 2-Iodoacetamide manufacturers

Shaanxi Dideu Medichem Co. Ltd
Product
2-Iodoacetamide 144-48-9
Price
US $0.00-0.00/KG
Min. Order
5mg
Purity
99% HPLC
Supply Ability
2000tons
Release date
2019-12-30
Hebei Yanxi Chemical Co., Ltd.
Product
2-Iodoacetamide 144-48-9
Price
US $0.00/kg
Min. Order
1kg
Purity
0.99
Supply Ability
20 tons
Release date
2023-11-21
Hebei Mojin Biotechnology Co., Ltd
Product
2-Iodoacetamide 144-48-9
Price
US $0.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
50000KG/month
Release date
2023-11-20

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