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Merck
CN

485705

Sigma-Aldrich

Formic-d acid

95 wt. % in H2O, 98 atom % D

Synonym(s):

Deuterated formic acid

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About This Item

Linear Formula:
DCO2H
CAS Number:
Molecular Weight:
47.03
MDL number:
UNSPSC Code:
12352106
PubChem Substance ID:
NACRES:
NA.12
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isotopic purity

98 atom % D

Quality Level

Assay

99% (CP)

concentration

95 wt. % in H2O

refractive index

n20/D 1.369

bp

100.8 °C (lit.)

mp

8.2-8.4 °C (lit.)

density

1.246 g/mL at 25 °C

mass shift

M+1

SMILES string

[2H]C(O)=O

InChI

1S/CH2O2/c2-1-3/h1H,(H,2,3)/i1D

InChI key

BDAGIHXWWSANSR-MICDWDOJSA-N

Application

- Quality control reference standards
- Analytical method development
- Pharmaceutical formulation development
- Environmental monitoring applications

Features and Benefits

Features
- High reactivity for diverse applications
- Supports innovative pharmaceutical research
- Produces minimal by-products in reactions
- Suitable for various biological studies

Benefits
- Streamlines the pharmaceutical development process
- Enhances effectiveness of biological assays
- Improves accuracy in metabolic studies
- Supports advancements in personalized medicine

Packaging

This product may be available from bulk stock and can be packaged on demand. For information on pricing, availability and packaging, please contact Stable Isotopes Customer Service.

Signal Word

Danger

Hazard Statements

Hazard Classifications

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

Storage Class Code

3 - Flammable liquids

WGK

WGK 1

Flash Point(F)

123.8 °F

Flash Point(C)

51 °C

Regulatory Information

美国出口管控产品
危险化学品

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Ana Celia Muñoz-Muñoz et al.
Journal of analytical toxicology, 44(1), 36-40 (2019-07-03)
An amphetamine interference was observed during the development of an liquid chromatography-high-resolution mass spectrometry (LC-HRMS) multi-class confirmation method for the determination of 47 drugs and metabolites in urine. The interference passed all qualitative criteria for amphetamine leading to potential false-positive
Masayuki Iguchi et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 23(67), 17017-17021 (2017-08-05)
Kinetic studies on the catalytic reaction mechanism of formic acid (FA) dehydrogenation were performed in the presence of a water-soluble iridium complex bearing a 4,4'-dihydroxy-2,2'-bipyridine ligand. Determination of kinetic isotope effects revealed that a shift of the rate-limiting step at
Ying Zhang et al.
The Analyst, 145(13), 4442-4451 (2020-06-13)
Hydrotreatment is extensively used for the production of clean fuel. Attaining an understanding of the structural conversion of the nitrogen species during hydrotreatment is very challenging due to the compositional complexity and the absence of a proper characterization method. In
Agnieszka Piegat et al.
Molecules (Basel, Switzerland), 24(17) (2019-08-25)
The structure of acylated chitosan derivatives strongly determines the properties of obtained products, influencing their hydrodynamic properties and thereby their solubility or self-assembly susceptibility. In the present work, the significance of slight changes in acylation conditions on the structure and
Rose M Gathungu et al.
Analytical chemistry, 88(18), 9103-9110 (2016-08-18)
Lipids from different classes sometimes can exhibit the same exact mass upon electrospray ionization; this presents an analytical challenge in lipidomics. In the negative ionization mode, for example, this can occur with phosphatidylcholines (PCs) and phosphatidylserines (PSs), making them indistinguishable

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