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

CAS: 141-53-7 Cat. No.: S104881 Formule: CHNaO₂ Poids moléculaire: 68.01 Beilstein Registry Number: 3595134 Numéro 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

Synonymes

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 |

Spécifications et pureté

PrimorTrace™, ≥99.99% metals basis

Conditions de stockage de stockage

Desiccated,Room temperature

Expédié en

Normal

Grade

PrimorTrace™

Pureté

≥99.99% metals basis

Noms et identifiants

Pubchem Sid

508814978

Sourires canoniques

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

Isomères SMILES

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

WGK Allemagne

1

RTECS

LR0350000

Poids moléculaire

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
• Description: 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

Cibles associées (humaines)

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

Cibles associées (non humaines)

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

Mécanismes d'action

Propriétés chimiques et physiques

• Sensibilité: moisture sensitive
• Point d'ébullition (°C): 360°C
• Point de fusion (°C): 253°C
• Poids moléculaire: 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

XLogP3