F0507
Formic acid
reagent grade, ≥95%
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크기 선택
제품정보 (DICE 배송 시 비용 별도)
Linear Formula:
HCOOH
CAS 번호:
Molecular Weight:
46.03
Beilstein:
1209246
EC Number:
MDL number:
UNSPSC 코드:
12352106
PubChem Substance ID:
NACRES:
NA.21
Grade
reagent grade
Quality Level
vapor density
1.6 (vs air)
vapor pressure
44.8 mmHg ( 20 °C)
분석
≥95%
양식
liquid
autoignition temp.
1004 °F
포함
<2.5% water as stabilizer
expl. lim.
57 %
환경친화적 대안 제품 특성
Catalysis
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sustainability
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불순물
≤1% acetic acid
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.)
환경친화적 대안 카테고리
저장 온도
room temp
SMILES string
OC=O
InChI
1S/CH2O2/c2-1-3/h1H,(H,2,3)
InChI key
BDAGIHXWWSANSR-UHFFFAOYSA-N
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일반 설명
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.
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애플리케이션
- 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).
Formic acid is used as a reducing agent in the:
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.
- synthesis of graphene from graphene oxide.
- catalytic reduction of chromium (Cr(VI) to Cr(III)) by colloidal palladium.
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.
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1A
보충제 위험성
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
Tissue distribution, effects of cooking and parameters affecting the extraction of azaspiracids from mussels, Mytilus edulis, prior to analysis by liquid chromatography coupled to mass spectrometry.
Hess P et al.
Toxicon, 46, 62-62 (2005)
Protocol for the induction of arthritis in C57BL/6 mice.
Inglis JJ et al.
Nature Protocols, 612-612 (2008)
Separation and Detection of Phosphorylated and Nonphosphorylated BvgA, a Bordetella pertussis Response Regulator, in vivo and in vitro.
Chen Q et al.
Bio-protocol, 3 (2013)
Glucosinolates determination in tissues of horseradish Plant.
Lelario F et al.
Bio-protocol, 5, e1562-e1562 (2015)
Thomas S Dexheimer et al.
Nature protocols, 3(11), 1736-1750 (2008-10-18)
The inhibition of DNA topoisomerase I (Top1) has proven to be a successful approach in the design of anticancer agents. However, despite the clinical successes of the camptothecin derivatives, a significant need for less toxic and more chemically stable Top1
문서
LC-MS/MS-based determination of 19 sulfonamides, 13 quinolones, and 3 tetracycline drug residues in pork meat samples using Supel™ Swift HLB for extraction.
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