Sodium oxalate - PrimorTrace™, ≥99.99% metals basis , CAS No.62-76-0

CAS: 62-76-0 Cat. No.: S112353 Summenformel: C₂Na₂O₄ Molekulargewicht: 134.00 Beilstein Registry Number: 3631622 EG-Nummer: 200-550-3

GRADE & PURITY PrimorTrace™, ≥99.99% metals basis

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

Room temperature,Argon charged

Shipped In

Normal

Specifications

Synonyme

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

Spezifikationen & Reinheit

PrimorTrace™, ≥99.99% metals basis

Storage

Room temperature,Argon charged

Verschickt in

Normal

Note

PrimorTrace™

Reinheit

≥99.99% metals basis

Product Line

S112353-25g

Namen und Kennungen

Pubchem Sid

508816476

Kanonisches Lächeln

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

Isomere SMILES

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

Molekulargewicht

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
    • Klasse Carboxylic acids and derivatives
      • Subclass Dicarboxylic acids and derivatives

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Klasse: 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
• Beschreibung: 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

Zugehörige Ziele (menschlich)

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)

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

CA1 Tclin Carbonic anhydrase I (13240 Activities)

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

CA5A Tclin Carbonic anhydrase VA (1168 Activities)

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

CA9 Tclin Carbonic anhydrase IX (8255 Activities)

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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

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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

Wirkungsmechanismen

Chemische und physikalische Eigenschaften

• Empfindlichkeit: Moisture sensitive.
• Schmelzpunkt (°C): 250-270°C
• Molekulargewicht: 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