Sodium oxalate - ≥99% , CAS No.62-76-0

CAS: 62-76-0 Cat. No.: S299314 Formula: C₂Na₂O₄ Peso molecolare: 134.00 Beilstein Registry Number: 3631622 Numero EC: 200-550-3

GRADE & PURITY ≥99%

Synonyms

7U0V68LT9X | CHEBI:132764 | Oxalic acid, disodium salt | Sodium oxalate, ACS reagent, >=99.5% | Sodium oxalate, BioUltra, >=99.5% (RT) | Sodium oxalate, certified reference material for titrimetry, certified by BAM, according to ISO 17025, >=99.5% | Oxali

Storage

Argon charged,Room temperature

Shipped In

Normal

Panoramica

Sodium oxalate is a water soluble inorganic salt mainly used for the standardization of permanganate solution during titration.

Sodium oxalate is used as reducing agent, as a primary standard for standardizing potassium permanganate solutions and as a neutralizer for exothermic acidic reactions. It finds application in metal cleaning preparations, metal extraction and separation, blueprint coatings, electroplating baths, special cement manufacturing, plant nutrition as well as in textile and pharmaceutical industries. It plays an important role to remove calcium ions from blood plasma and prevents blood clotting.

Specifications

Sinonimi

7U0V68LT9X | CHEBI:132764 | Oxalic acid, disodium salt | Sodium oxalate, ACS reagent, >=99.5% | Sodium oxalate, BioUltra, >=99.5% (RT) | Sodium oxalate, certified reference material for titrimetry, certified by BAM, according to ISO 17025, >=99.5% | Oxali

Specifiche e purezza

≥99%

Condizioni di conservazione di stoccaggio

Argon charged,Room temperature

Spedito in

Normal

Purezza

≥99%

Nomi e identificatori

Pubchem Sid

504751005

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/504751005

Sorrisi canonici

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

IUPAC Name

disodium;oxalate

InChIKey

ZNCPFRVNHGOPAG-UHFFFAOYSA-L

INCHI

1S/C2H2O4.2Na/c3-1(4)2(5)6;;/h(H,3,4)(H,5,6);;/q;2*+1/p-2

Isomeri SMILES

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

Peso molecolare

134.00

Beilstein

3631622

Reaxy-Rn

3631622

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3631622&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Classe Carboxylic acids and derivatives
      • Subclass Dicarboxylic acids and derivatives

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Classe: Carboxylic acids and derivatives
• Subclass: Dicarboxylic acids and derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Dicarboxylic acids and derivatives
• Alternative Parents: Carboxylic acid salts Carboxylic acids Organic sodium salts Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Dicarboxylic acid or derivatives - Carboxylic acid salt - Organic alkali metal salt - Carboxylic acid - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organic sodium salt - Organic salt - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as dicarboxylic acids and derivatives. These are organic compounds containing exactly two carboxylic acid groups.
• 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

Obiettivi associati (umani)

CA4 Tclin Carbonic anhydrase 4 (1 Activities)

Discover Target: CA4

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

CA2 Tclin Carbonic anhydrase II (17698 Activities)

Discover Target: CA2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CA1 Tclin Carbonic anhydrase I (13240 Activities)

Discover Target: CA1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CA5A Tclin Carbonic anhydrase VA (1168 Activities)

Discover Target: CA5A

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CA9 Tclin Carbonic anhydrase IX (8255 Activities)

Discover Target: CA9

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

FFAR3 Tchem Free fatty acid receptor 3 (304 Activities)

Discover Target: FFAR3

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

SLC22A8 Tclin Solute carrier family 22 member 8 (241 Activities)

Discover Target: SLC22A8

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Obiettivi associati (non umani)

CA4 Carbonic anhydrase IV (1713 Activities)

Discover Target: CA4

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Carbonic anhydrase (69 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Meccanismi d'azione

Proprietà chimiche e fisiche

• Solubilità: Soluble in water and formic acid. Insoluble in ether and alcohol.
• Sensibilità: Moisture sensitive
• Punto di fusione (°C): 250-270°C
• Peso molecolare: 134.000 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 0
• Exact Mass: 133.959 Da
• Monoisotopic Mass: 133.959 Da
• Topological Polar Surface Area: 80.300 Ų
• Heavy Atom Count: 8
• Formal Charge: 0
• Complexity: 60.500
• 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: 3

XLogP3

Domande frequenti

How is this product shipped?

This product ships under standard ambient conditions. No temperature-controlled packaging is required.