Formate（FA） - UltraPureChrom™, for LC-MS, ≥99% , CAS No.64-18-6

CAS: 64-18-6 Cat. No.: F301957 Fórmula: CH₂O₂ Peso molecular: 46.03 Beilstein Registry Number: 1209246 Número EC: 200-579-1

CALIDAD & PUREZA UltraPureChrom™, for LC-MS, ≥99%

Synonyms

Formic Acid

Storage

Room temperature,Argon charged

Shipped In

FedEx DG Service

Especificaciones

Sinónimos

Formic Acid

Especificaciones y pureza

UltraPureChrom™, for LC-MS, ≥99%

Condiciones de almacenamiento de almacenamiento

Room temperature,Argon charged

Enviado en

FedEx DG Service

Grado

for LC-MS, UltraPureChrom™

Pureza

≥99%

Nombres e identificadores

Pubchem Sid

508814970

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/508814970

Sonrisas canónicas

C(=O)O

IUPAC Name

formic acid

InChIKey

BDAGIHXWWSANSR-UHFFFAOYSA-N

INCHI

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

Isómeros SMILES

C(=O)O

WGK Alemania

1

Número ONU

1779

Grupo de embalaje

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
    • Clase Carboxylic acids and derivatives
      • Subclass Carboxylic acids

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Clase: 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
• Descripción: 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

Objetivos asociados (no 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 acción

Propiedades químicas y físicas

• Solubilidad: Miscible in water, ether, acetone, ethyl acetate, glycerol, methanol and ethanol. Partially miscible in benzene, toluene and xylene.
• Sensibilidad: Moisture sensitive.
• Índice de refracción: 1.3690 - 1.3730
• Punto de inflamación (°F): 121.1 °F
• Punto de inflamación (°C): 49.5 °C
• Punto de ebullición (°C): 100-101°C
• Punto de fusión (°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