Sodium iodoacetate - Moligand™, ≥98% , CAS No.305-53-3

CAS: 305-53-3 Cat. No.: S104897 Formule: C₂H₂INaO₂ Poids moléculaire: 207.93 Beilstein Registry Number: 4009322 Numéro CE: 206-165-7

QUALITÉ & PURETÉ Moligand™, ≥98%

Synonyms

EINECS 206-165-7 | E75848 | Iodoacetic acid sodium salt | MFCD00002686 | J-200341 | DTXSID0059790 | sodium;2-iodoacetate | sodiumiodoacetate | Q7763011 | A876151 | sodium iodoacetate | CCRIS 9232 | iodoacetate (Sodium) | Iodoacetic acid, sodium salt | FT-

Storage

Protected from light,Store at -20°C,Argon charged,Desiccated

Shipped In

Ice chest + Ice pads

Vue d’ensemble

A reagent used to modify cysteine residues in proteins to inhibit cysteine proteases.

Spécifications

Synonymes

EINECS 206-165-7 | E75848 | Iodoacetic acid sodium salt | MFCD00002686 | J-200341 | DTXSID0059790 | sodium;2-iodoacetate | sodiumiodoacetate | Q7763011 | A876151 | sodium iodoacetate | CCRIS 9232 | iodoacetate (Sodium) | Iodoacetic acid, sodium salt | FT-

Spécifications et pureté

Moligand™, ≥98%

Mécanismes biochimiques et physiologiques

Iodoacetic Acid, Sodium Salt is a reagent shown to be used to modify cysteine residues in proteins to ultimately inhibit cysteine proteases. Iodoacetic Acid, Sodium Salt has been observed to slightly inhibit the O-hexyl O-2,5-dichlorophenyl phosphoramidat

Conditions de stockage de stockage

Protected from light,Store at -20°C,Argon charged,Desiccated

Expédié en

Ice chest + Ice pads

Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.

Grade

Moligand™

Type d'action

INHIBITOR

Note

Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Toxic, refer to SDS for further information. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.

Pureté

≥98%

Noms et identifiants

Pubchem Sid

528774187

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/528774187

Sourires canoniques

C(C(=O)[O-])I.[Na+]

IUPAC Name

sodium;2-iodoacetate

InChIKey

AGDSCTQQXMDDCV-UHFFFAOYSA-M

INCHI

1S/C2H3IO2.Na/c3-1-2(4)5;/h1H2,(H,4,5);/q;+1/p-1

Isomères SMILES

C(C(=O)[O-])I.[Na+]

WGK Allemagne

3

RTECS

AI3675000

Numéro ONU

2811

Poids moléculaire

207.93

Beilstein

4009322

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Classe Carboxylic acids and derivatives
      • Subclass Alpha-halocarboxylic acids and derivatives

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Classe: 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

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Propriétés chimiques et physiques

• Solubilité: Soluble in H2O
• Sensibilité: Light Sensitive,Hygroscopic
• Point de fusion (°C): 208°C
• Poids moléculaire: 207.930 g/mol
• 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

XLogP3