Formic acid（FA） - ACS, ≥88% , CAS No.64-18-6

CAS: 64-18-6 Cat. No.: F112035 Formula: CH₂O₂ Peso molecolare: 46.03 Beilstein Registry Number: 1209246 Numero EC: 200-579-1

QUALITÀ & PUREZZA ACS, ≥88%

Synonyms

FORMIC ACID [EP MONOGRAPH] | Acidum formicum | CCG-266004 | Formic acid, purum, >=85% | FORMICUM ACIDUM [HPUS] | Kyselina mravenci [Czech] | STL264243 | FORMIC ACID [INCI] | Formic acid, ACS reagent, >=96.0% | FORMIC ACID [HSDB] | Formic acid, AR, >=98% |

Storage

Room temperature,Argon charged

Shipped In

FedEx DG Service

Specifiche

Sinonimi

FORMIC ACID [EP MONOGRAPH] | Acidum formicum | CCG-266004 | Formic acid, purum, >=85% | FORMICUM ACIDUM [HPUS] | Kyselina mravenci [Czech] | STL264243 | FORMIC ACID [INCI] | Formic acid, ACS reagent, >=96.0% | FORMIC ACID [HSDB] | Formic acid, AR, >=98% |

Specifiche e purezza

ACS, ≥88%

Condizioni di conservazione di stoccaggio

Room temperature,Argon charged

Spedito in

FedEx DG Service

Grado

ACS

Purezza

≥88%

Nomi e identificatori

Pubchem Sid

508814969

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/508814969

Sorrisi canonici

C(=O)O

IUPAC Name

formic acid

InChIKey

BDAGIHXWWSANSR-UHFFFAOYSA-N

INCHI

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

Isomeri SMILES

C(=O)O

WGK Germania

1

Numero UN

1779

Gruppo di imballaggio

II

Peso molecolare

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
• Descrizione: 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

Obiettivi associati (non umani)

Drosophila melanogaster (359 Activities)

Explore this target

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

Meccanismi d'azione

Proprietà chimiche e fisiche

• Solubilità: Miscible in water, ether, acetone, ethyl acetate, glycerol, methanol and ethanol. Partially miscible in benzene, toluene and xylene.
• Sensibilità: moisture sensitive
• Indice di rifrazione: 1.3690 - 1.3730
• Punto di infiammabilità (°F): 121.1 °F
• Punto di infiammabilità (°C): 49.5 °C
• Punto di ebollizione (°C): 100-101°C
• Punto di fusione (°C): 8.2-8.4°C
• Peso molecolare: 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