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

CAS: 64-18-6 Cat. No.: F112034 Fórmula: CH₂O₂ Peso molecular: 46.03 Beilstein Registry Number: 1209246 Número CE: 200-579-1

GRAU & PUREZA UltraPureChrom™, for HPLC

Synonyms

Formylic acid | Methanoic acid

Storage

Room temperature,Argon charged

Shipped In

FedEx DG Service

Especificações

Sinónimos

Formylic acid | Methanoic acid

Especificações e pureza

UltraPureChrom™, for HPLC

Condições de armazenamento de armazenamento

Room temperature,Argon charged

Enviado em

FedEx DG Service

Grau

for HPLC, UltraPureChrom™

Nomes e identificadores

Pubchem Sid

508814972

Pubchem Sid Url

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

Sorrisos canónicos

C(=O)O

IUPAC Name

formic acid

InChIKey

BDAGIHXWWSANSR-UHFFFAOYSA-N

INCHI

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

SMILES isoméricas

C(=O)O

WGK Alemanha

1

Número UN

1779

Grupo de embalagem

II

Peso molecular

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
    • Classe Carboxylic acids and derivatives
      • Subclass Carboxylic acids

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Classe: 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
• Descrição: 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

Alvos associados (não humanos)

Drosophila melanogaster (359 Activities)

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

Mecanismos de ação

Propriedades químicas e físicas

• Solubilidade: Solubility in water: Completely miscible; Miscible with Ether,Ethanol,Methanol; Soluble in Benzene,Toluene
• Sensibilidade: Hygroscopic
• Índice de refração: 1.3690 - 1.3730
• Ponto de inflamação (°F): 121.1 °F
• Ponto de inflamação (°C): 49.5 °C
• Ponto de ebulição (°C): 100-101°C
• Ponto de fusão (°C): 8.2-8.4°C
• Peso molecular: 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