Formic acid（FA） - ≥85%, used for Formic acid can be used as a reagent for: carbonyl compounds and nitro compounds Co-Nx-catalyzed one-pot reductive amination for the synthesis of secondary amines. The photoreduction of polycyclic and heterocyclic nitroaro

CAS: 64-18-6 Cat. No.: F301789 Formula: CH₂O₂ Peso molecolare: 46.03 Beilstein Registry Number: 1209246 Numero EC: 200-579-1

QUALITÀ & PUREZZA ≥85%

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,Desiccated

Shipped In

FedEx DG Service

Panoramica

It can be freely mixed with water, alcohols, ethers, and glycerol, and is corrosive to the skin. It serves as a reducing agent for determining arsenic, bismuth, aluminum, copper, gold, indium, iron, lead, manganese, mercury, molybdenum, silver, and zinc, as well as for testing cerium, rhenium, and tungsten. It is used to test aromatic primary and secondary amines, measure molecular weights and crystallization solvents, determine methoxy groups, act as a fixative in microanalysis, and in the production of formate salts.

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

≥85%

Applicazione

Formic acid can be used as a reagent for: carbonyl compounds and nitro compounds Co-Nx-catalyzed one-pot reductive amination for the synthesis of secondary amines. The photoreduction of polycyclic and heterocyclic nitroaromatics yields the corresponding a

Condizioni di conservazione di stoccaggio

Room temperature,Argon charged,Desiccated

Spedito in

FedEx DG Service

Purezza

≥85%

Nomi e identificatori

Pubchem Sid

508814990

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/508814990

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)

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

Meccanismi d'azione

Proprietà chimiche e fisiche

• Sensibilità: Moisture sensitive. ;heat 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