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695076

Sigma-Aldrich

Formic acid

ACS reagent, ≥96%

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About This Item

Linear Formula:
HCOOH
CAS Number:
64-18-6
Molecular Weight:
46.03
Beilstein:
1209246
EC Number:
200-579-1
MDL number:
MFCD00003297
UNSPSC Code:
12352106
PubChem Substance ID:
329761713
NACRES:
NA.21

grade

ACS reagent

Quality Level

200

vapor density

1.6 (vs air)

vapor pressure

44.8 mmHg ( 20 °C)

Assay

≥96%

form

liquid

autoignition temp.

1004 °F

expl. lim.

57 %

refractive index

n20/D 1.370 (lit.)

pH

2.2 (20 °C, 2.2 g/L)

bp

100-101 °C (lit.)

mp

8.2-8.4 °C (lit.)

solubility

water: miscible

density

1.22 g/mL at 25 °C (lit.)

anion traces

chloride (Cl-): ≤0.001%
sulfate (SO42-): ≤0.003%
sulfite (SO32-): passes test

cation traces

Fe: ≤0.001%
NH4+: ≤0.005%
heavy metals (as Pb): ≤0.001%

application(s)

sample preparation

SMILES string

OC=O

InChI

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

InChI key

BDAGIHXWWSANSR-UHFFFAOYSA-N

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General description

Formic acid is a simple carboxylic acid produced by the hydrolysis of methyl formate or formamide or from its salts. It is primarily used in dyeing, textile, leather, rubber, chemical, and pharmaceutical industries.

Application

Formic acid can be used as a reagent in the:
  • Co-Nx-catalyzed one-pot reductive amination of carbonyl compounds with nitro compounds to synthesize secondary amines.
  • Photoreduction of polycyclic and heterocyclic nitro arenes to corresponding amines.
  • Pd-catalyzed chemoselective hydrogenation of olefins to saturated hydrocarbons.

Signal Word

Danger

Hazard Statements

H226 - H302 - H314 - H331

Hazard Classifications

Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1A

Supplementary Hazards

EUH071

Storage Class Code

3 - Flammable liquids

WGK

WGK 1

Flash Point(F)

121.1 °F - closed cup

Flash Point(C)

49.5 °C - closed cup

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Sarela García-Santamarina et al.
Nature protocols, 9(5), 1131-1145 (2014-04-20)
Reversible thiol oxidation of cysteine residues occurs in many intracellular catalytic and signaling processes. Here we describe an optimized protocol, which can be completed in ∼5 d, to unambiguously identify specific cysteine residues that are transiently and reversibly oxidized by
The crystal structure of formic acid.
Holtzberg F, et al.
Acta Crystallographica, 6(2), 127-130 (1953)
Photodissociation of formic acid.
Su H, et al.
J. Chem. Phys., 113(5), 1891-1897 (2000)
Electron momentum spectroscopy of formic acid.
Nixon KL, et al.
Chemical Physics Letters, 474(1), 23-27 (2009)
Direct formic acid fuel cells.
Rice C, et al.
Journal of Power Sources, 111(1), 83-89 (2002)
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