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Merck

399388

Ácido fórmico

greener alternative

ACS reagent, ≥88%

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About This Item

Fórmula lineal:
HCOOH
Número CAS:
Peso molecular:
46.03
UNSPSC Code:
12352106
NACRES:
NA.21
PubChem Substance ID:
EC Number:
200-579-1
Beilstein/REAXYS Number:
1209246
MDL number:

Nombre del producto

Ácido fórmico, ACS reagent, ≥88%

InChI key

BDAGIHXWWSANSR-UHFFFAOYSA-N

InChI

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

SMILES string

OC=O

grade

ACS reagent

vapor density

1.6 (vs air)

vapor pressure

44.8 mmHg ( 20 °C)

description

dilution test passes test

assay

≥88%

form

liquid

autoignition temp.

1004 °F

expl. lim.

57 %

greener alternative product characteristics

Catalysis
Learn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

impurities

≤0.4% Acetic acid

evapn. residue

≤0.002%

color

APHA: ≤15

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-): ≤0.002%
sulfite (SO32-): passes test

cation traces

Fe: ≤5 ppm
NH4+: ≤0.005%
heavy metals: ≤5 ppm (by ICP)

greener alternative category

storage temp.

room temp

Quality Level

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Categorías relacionadas

Application

Reductant used in iron-catalyzed, greener reduction of aldehydes to alcohols .

Fast and selective iron-catalyzed transfer hydrogenations of aldehydes

General description

We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product has been enhanced for catalysis. Click here for more information.

signalword

Danger

Hazard Classifications

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

supp_hazards

Clase de almacenamiento

3 - Flammable liquids

wgk

WGK 3

flash_point_f

118.4 °F

flash_point_c

48 °C


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Modification of Pd for formic acid decomposition by support grafted functional groups.
Jones S, et al.
Catalysis, Structure & Reactivity, 1(1), 19-24 (2015)
Carbon dioxide as a raw material: the synthesis of formic acid and its derivatives from CO2.
Leitner W.
Angewandte Chemie (International Edition in English), 34(20), 2207-2221 (1995)
T Kitamoto et al.
Laboratory investigation; a journal of technical methods and pathology, 57(2), 230-236 (1987-08-01)
The purpose of this study was to design a method by which immunoperoxidase staining can be applied to formalin-fixed, paraffin-embedded tissue sections to demonstrate amyloid deposits in cerebral and systemic amyloidotic tissues. We used anti-prion protein, anti-beta-protein, anti-amyloid A, and
Advances in Direct Formic Acid Fuel Cells: Fabrication of Efficient Ir/Pd Nanocatalysts for Formic Acid Electro-Oxidation.
Al-Akraa IM, et al.
International Journal of Electrochemical Science, 10, 3282-3290 (2015)
Pd-Cu/C electrocatalysts synthesized by one-pot polyol reduction toward formic acid oxidation: Structural characterization and electrocatalytic performance.
Wang L, et al.
International Journal of Hydrogen Energy, 40(4), 1726-1734 (2015)

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