Sodium formate - ≥99.5% , CAS No.141-53-7

CAS: 141-53-7 Cat. No.: S164504 Formula: CHNaO₂ Molecular Weight: 68.01 Beilstein Registry Number: 3595134 EC Number: 205-488-0

GRADE & PURITY ≥99.5%

Synonyms

SODIUM FORMATE|141-53-7|Formic acid, sodium salt|Formic acid sodium salt|Salachlor|FORMIC ACID, NA SALT|sodium formiate|Formic acid, sodium salt (1:1)|Sodium formate, refined|MFCD00013101|CHEBI:62965|387AD98770|sodium;formate|Mravencan sodny|Mravencan sod

Storage

Argon charged,Room temperature

Shipped In

Normal

Overview

Sodium formate is a versatile chemical used in many laboratory techniques including crystallization, molecule-based material construction, and chemiluminescence. Sodium formate is an intermediate involved in making of formic acid, oxalic acid, and sodium dithionite. Buffering agent for strong mineral acids and noble metals. Sodium formate has been shown to act as a sigmal for Salmonella invasion. Sodium formate also acts as a free radical scavenger.
A versitile formate compound employed in laboratory techniques

Specifications

Synonyms

SODIUM FORMATE | 141-53-7 | Formic acid, sodium salt | Formic acid sodium salt | Salachlor | FORMIC ACID, NA SALT | sodium formiate | Formic acid, sodium salt (1:1) | Sodium formate, refined | MFCD00013101 | CHEBI:62965 | 387AD98770 | sodium;formate | Mravencan sodny | Mravencan sod

Specifications & Purity

≥99.5%

Storage

Argon charged,Room temperature

Shipped In

Normal

Purity

≥99.5%

Names and Identifiers

• Pubchem Sid: 504760813
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504760813
• Canonical Smiles: 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
• Isomeric SMILES: C(=O)[O-].[Na+]
• WGK Germany: 1
• RTECS: LR0350000
• Molecular Weight: 68.01
• Beilstein: 3595134

Taxonomic Classification

Taxonomy Tree

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

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

Associated Targets(Human)

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

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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

Associated Targets(non-human)

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

Mechanisms of Action

Chemical and Physical Properties

• Solubility: Soluble in water (970 mg/ml at 20 °C), glycerol, and alcohol (slightly). Insoluble in ether.
• Sensitivity: Moisture sensitive
• x_boil_point_char: 360°C
• x_melt_point_char: 253°C
• Molecular Weight: 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

Frequently Asked Questions

What is the purity of this product?

This product is supplied at ≥99.5% purity (chemical assay). Lot-specific values are stated on the Certificate of Analysis.

How should this product be stored?

Store at room temperature under argon. It is supplied under an argon blanket; reseal under inert gas after each use.

How is this product shipped?

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

What are the CAS number, molecular formula and molecular weight?

The CAS Number is 141-53-7, the molecular formula is CHNaO2, and the molecular weight is 68.01 g/mol. InChIKey HLBBKKJFGFRGMU-UHFFFAOYSA-M.

What documentation is provided?

Available product documentation, including Certificates of Analysis (COA), Safety Data Sheets (SDS), and specification sheets, is shown in the product document area. Document availability and access follow the current site policy.