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Formic acid

SIGALD/F0507 - reagent grade, ≥95%

CAS Number: 64-18-6
Empirical Formula (Hill Notation): CH2O2
Molecular Weight: 46.03
EC Number: 200-579-1
MDL Number: MFCD00003297
Linear Formula: HCOOH
Product Type: Chemical

Catalog Number PKG Qty. Price Quantity
45-F0507-100ML 100 mL
$52.20
1/EA
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45-F0507-4X100ML 100 mL
$161.00
4/EA
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45-F0507-500ML 500 mL
$85.20
1/EA
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45-F0507-1L 1 L
$164.00
1/EA
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45-F0507-4L 4 L
$542.00
1/EA
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4×100 Slip-cover Can
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assay ≥95%
autoignition temp. 1004 °F
bp 100-101 °C (lit.)
contains <2.5% water as stabilizer
density 1.22 g/mL at 25 °C (lit.)
expl. lim. 57 %
form liquid
grade reagent grade
impurities ≤1% acetic acid
InChI 1S/CH2O2/c2-1-3/h1H,(H,2,3)
InChI key BDAGIHXWWSANSR-UHFFFAOYSA-N
mp 8.2-8.4 °C (lit.)
pH 2.2 (20 °C, 2.2 g/L)
Quality Level 100 
refractive index n20/D 1.370 (lit.)
SMILES string OC=O
storage temp. room temp
vapor density 1.6 (vs air)
vapor pressure 44.8 mmHg ( 20 °C)
Application:

  • Electrochemical CO(2) Reduction on Metallic and Oxidized Tin: This study uses grand-canonical density functional theory (DFT) and in situ attenuated total reflectance surface-enhanced infrared absorption spectroscopy (ATR-SEIRA) to investigate electrochemical carbon dioxide reduction on tin surfaces, where formic acid could play a role in understanding reaction mechanisms (Whittaker et al., 2024 ).

  • Simultaneous Measurement of COVID-19 Treatment Drugs: This research demonstrates the use of UPLC-MS/MS for the simultaneous measurement of COVID-19 treatment drugs in rat plasma, indicating the importance of formic acid in preparing samples or as a mobile phase additive for better chromatographic separation (Zhou et al., 2024 ).

  • Metabolite Profiling of Liquiritin: The study involves metabolite profiling using ultra-high-performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS), where formic acid is likely utilized in sample preparation or chromatographic processes (Chen et al., 2024 ).

  • Analysis of Cocaine and Its Metabolites: This article explores solid-phase extraction followed by UHPLC-ESI-MS/MS analysis of cocaine metabolites, a method that often incorporates formic acid to enhance the ionization of analytes (Makhdoom et al., 2024 ).

  • Determination of Antimicrobial Compounds in Pigs: This research uses UHPLC-MS/MS for the simultaneous determination of various antimicrobial compounds, demonstrating formic acid′s role in sample processing and chromatographic separation (Nowacka-Kozak et al., 2024 ).

Application: Formic acid is used as a reducing agent in the:

• synthesis of graphene from graphene oxide.
• catalytic reduction of chromium (Cr(VI) to Cr(III)) by colloidal palladium.
It is also used as a reagent in the Eschweiler-Clarke reaction during the synthesis of ketamine from the reduction of 2-(2-chlorophenyl)-2-nitrocyclohexanone (2-CPNCH) to norketamine.

Additionally, it is used as a hydrogen donor during the transformation of the furanose form into the pyranose form of glucose and in the catalytic transfer hydrogenation reaction.
General description: Formic acid (HCOOH, FA) is the simplest carboxylic acid that is mostly found in insect bites and stings. It is widely utilized as a hydrogen storage molecule due to its low toxicity, recyclability, ease of usage, and liquid state in ambient conditions.
Packaging: 1, 4 L in poly bottle
Packaging: 100, 4×100, 500 mL in poly bottle
Purity ≥95%
bp 100-101 °C (lit.)
mp 8.2-8.4 °C (lit.)
Density 1.22 g/mL at 25 °C (lit.)
Refractive Index n20/D 1.370 (lit.)
Storage Temp. room temp
UNSPSC 12352106

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