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Sodium iodoacetate - UltraBio™, ≥99.5%(NT), high purity , CAS No.305-53-3

In stock
Item Number
S755677
Grouped product items
SKU Size
Availability
Price Qty
S755677-5g
5g
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$91.90
S755677-25g
25g
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$366.90

Basic Description

Specifications & Purity UltraBio™, ≥99.5%(NT)
Storage Temp Store at -20°C
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Grade UltraBio™
Product Description

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.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organic acids and derivatives
Class Carboxylic acids and derivatives
Subclass Alpha-halocarboxylic acids and derivatives
Intermediate Tree Nodes Not available
Direct Parent Alpha-halocarboxylic acids
Alternative Parents Carboxylic acid salts  Organic metal halides  Monocarboxylic acids and derivatives  Carboxylic acids  Organoiodides  Organic sodium salts  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  Alkyl iodides  
Molecular Framework Aliphatic acyclic compounds
Substituents Alpha-halocarboxylic acid - Carboxylic acid salt - Organic metal halide - Carboxylic acid - Organic alkali metal salt - Monocarboxylic acid or derivatives - Alkyl halide - Organic salt - Organooxygen compound - Organoiodide - Organohalogen compound - Organic sodium salt - Hydrocarbon derivative - Organic oxide - Carbonyl group - Organic oxygen compound - Alkyl iodide - Aliphatic acyclic compound
Description This compound belongs to the class of organic compounds known as alpha-halocarboxylic acids. These are carboxylic acids containing a halogen atom bonded to the alpha carbon atom.
External Descriptors Not available

Names and Identifiers

IUPAC Name sodium;2-iodoacetate
INCHI InChI=1S/C2H3IO2.Na/c3-1-2(4)5;/h1H2,(H,4,5);/q;+1/p-1
InChIKey AGDSCTQQXMDDCV-UHFFFAOYSA-M
Smiles C(C(=O)[O-])I.[Na+]
Isomeric SMILES C(C(=O)[O-])I.[Na+]
WGK Germany 3
RTECS AI3675000
PubChem CID 5239
UN Number 2811
Molecular Weight 207.93
Beilstein 4009322

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Chemical and Physical Properties

Solubility methanol: 0.1 M at 20 °C, clear, colorless
Melt Point(°C) 208°C
Molecular Weight 207.930 g/mol
XLogP3
Hydrogen Bond Donor Count 0
Hydrogen Bond Acceptor Count 2
Rotatable Bond Count 1
Exact Mass 207.9 Da
Monoisotopic Mass 207.9 Da
Topological Polar Surface Area 40.100 Ų
Heavy Atom Count 6
Formal Charge 0
Complexity 46.800
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 2

Citations of This Product

1. Jiamei LI, An YAN, Mingquan WANG, Di LI.  (2024)  Aptamer and phosphorothioated DNA engineered liposomes as a targeted intracellular protein delivery system.  CHINESE JOURNAL OF ANALYTICAL CHEMISTRY,  52  (100400). 

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