Sodium formate - PrimorTrace™, ≥99.99% metals basis , CAS No.141-53-7

CAS: 141-53-7 Cat. No.: S104881 Fórmula: CHNaO₂ Peso molecular: 68.01 Beilstein Registry Number: 3595134 Número CE: 205-488-0

GRADE & PURITY PrimorTrace™, ≥99.99% metals basis

Synonyms

Sodium formate, refined | Mravencan sodny [Czech] | sodium formiate | AKOS015902050 | HSDB 744 | Mravencan sodny | sodium carbanate | DTXSID2027090 | MFCD00013101 | SODIUM FORMATE [HSDB] | CHNaO2 | NSC 77457 | MFCD00075589 | HLBBKKJFGFRGMU-UHFFFAOYSA-M |

Storage

Desiccated,Room temperature

Shipped In

Normal

Specifications

Sinónimos

Sodium formate, refined | Mravencan sodny [Czech] | sodium formiate | AKOS015902050 | HSDB 744 | Mravencan sodny | sodium carbanate | DTXSID2027090 | MFCD00013101 | SODIUM FORMATE [HSDB] | CHNaO2 | NSC 77457 | MFCD00075589 | HLBBKKJFGFRGMU-UHFFFAOYSA-M |

Especificações e pureza

PrimorTrace™, ≥99.99% metals basis

Condições de armazenamento de armazenamento

Desiccated,Room temperature

Enviado em

Normal

Grau

PrimorTrace™

Pureza

≥99.99% metals basis

Nomes e identificadores

• Pubchem Sid: 508814978
• Sorrisos canónicos: C(=O)[O-].[Na+]
• IUPAC Name: sodium;formate
• InChIKey: HLBBKKJFGFRGMU-UHFFFAOYSA-M
• INCHI: 1S/CH2O2.Na/c2-1-3;/h1H,(H,2,3);/q;+1/p-1
• SMILES isoméricas: C(=O)[O-].[Na+]
• WGK Alemanha: 1
• RTECS: LR0350000
• Peso molecular: 68.01
• Beilstein: 3595134

Taxonomic Classification

Taxonomy Tree

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

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

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

Alvos associados (humanos)

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

SLC16A3 Tchem Monocarboxylate transporter 4 (196 Activities)

Discover Target: SLC16A3

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

Alvos associados (não humanos)

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

Mecanismos de ação

Propriedades químicas e físicas

• Sensibilidade: moisture sensitive
• Ponto de ebulição (°C): 360°C
• Ponto de fusão (°C): 253°C
• Peso molecular: 68.007 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 0
• Exact Mass: 67.9874 Da
• Monoisotopic Mass: 67.9874 Da
• Topological Polar Surface Area: 40.100 Ų
• Heavy Atom Count: 4
• Formal Charge: 0
• Complexity: 13.500
• 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: 2

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