Formic Acid（FA） - UltraPureChrom™, for HPLC , CAS No.64-18-6

CAS: 64-18-6 Cat. No.: F112034 Formula: CH₂O₂ Molecular Weight: 46.03 Beilstein Registry Number: 1209246 EC Number: 200-579-1

GRADE & PURITY UltraPureChrom™, for HPLC

Synonyms

Formylic acid | Methanoic acid

Storage

Room temperature,Argon charged

Shipped In

FedEx DG Service

Specifications

Synonyms

Formylic acid | Methanoic acid

Specifications & Purity

UltraPureChrom™, for HPLC

Storage

Room temperature,Argon charged

Shipped In

FedEx DG Service

Grade

for HPLC, UltraPureChrom™

Names and Identifiers

Pubchem Sid

508814972

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/508814972

Canonical Smiles

C(=O)O

IUPAC Name

formic acid

InChIKey

BDAGIHXWWSANSR-UHFFFAOYSA-N

INCHI

1S/CH2O2/c2-1-3/h1H,(H,2,3)

Isomeric SMILES

C(=O)O

WGK Germany

1

UN Number

1779

Packing Group

II

Molecular Weight

46.03

Beilstein

1209246

Reaxy-Rn

1209246

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1209246&ln=

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Class: Carboxylic acids and derivatives
• Subclass: Carboxylic acids
• Intermediate Tree Nodes: Not available
• Direct Parent: Carboxylic acids
• Alternative Parents: Monocarboxylic acids and derivatives Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Monocarboxylic acid or derivatives - Carboxylic acid - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as carboxylic acids. These are compounds containing a carboxylic acid group with the formula -C(=O)OH.
• External Descriptors: Straight chain fatty acids - Saturated fatty acids

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(non-human)

Drosophila melanogaster (359 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: Solubility in water: Completely miscible; Miscible with Ether,Ethanol,Methanol; Soluble in Benzene,Toluene
• Sensitivity: Hygroscopic
• Refractive Index: 1.3690 - 1.3730
• Flash Point(°F): 121.1 °F
• Flash Point(°C): 49.5 °C
• Boil Point(°C): 100-101°C
• Melt Point(°C): 8.2-8.4°C
• Molecular Weight: 46.025 g/mol
• XLogP3: -0.200
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 0
• Exact Mass: 46.0055 Da
• Monoisotopic Mass: 46.0055 Da
• Topological Polar Surface Area: 37.300 Ų
• Heavy Atom Count: 3
• Formal Charge: 0
• Complexity: 10.300
• 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: 1