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Merck

70221

Supelco

Ammonium formate

eluent additive for LC-MS, LiChropur™, ≥99.0%

동의어(들):

Formic acid ammonium salt

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크기 선택

제품정보 (DICE 배송 시 비용 별도)

Linear Formula:
HCO2NH4
CAS 번호:
540-69-2
Molecular Weight:
63.06
Beilstein:
3625095
EC Number:
208-753-9
MDL number:
MFCD00013103
UNSPSC 코드:
12352107
eCl@ss:
39021903
PubChem Substance ID:
329762353
NACRES:
NB.21

주요 문서

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기술 서비스
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설명

anionic

Quality Level

100

제품 라인

LiChropur™

분석

≥99.0% (calc. on dry substance, NT)
≥99.0%

양식

crystals

품질

LiChropur™

기술

LC/MS: suitable

불순물

insoluble matter, passes filter test
<2% water

무기 잔류물(900 °C)

<0.1% (as SO4)

pH

5.5-7.5 (25 °C, 1 M in H2O)

mp

119-121 °C (lit.)

solubility

H2O: 1 M at 20 °C, clear, colorless

density

1.26 g/mL at 25 °C (lit.)

음이온 미량물

chloride (Cl-): ≤50 mg/kg
sulfate (SO42-): ≤50 mg/kg

양이온 미량물

Al: ≤1 mg/kg
As: ≤0.1 mg/kg
Ba: ≤1 mg/kg
Bi: ≤1 mg/kg
Ca: ≤5 mg/kg
Cd: ≤1 mg/kg
Co: ≤1 mg/kg
Cr: ≤1 mg/kg
Cu: ≤1 mg/kg
Fe: ≤1 mg/kg
K: ≤5 mg/kg
Li: ≤1 mg/kg
Mg: ≤1 mg/kg
Mn: ≤1 mg/kg
Mo: ≤1 mg/kg
Na: ≤5 mg/kg
Ni: ≤1 mg/kg
Pb: ≤1 mg/kg
Sr: ≤1 mg/kg
Zn: ≤1 mg/kg

λ

1 M in H2O

SMILES string

N.OC=O

UV 흡수

λ: 260 nm Amax: ≤0.01
λ: 280 nm Amax: ≤0.01

InChI

1S/CH2O2.H3N/c2-1-3;/h1H,(H,2,3);1H3

InChI key

VZTDIZULWFCMLS-UHFFFAOYSA-N

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관련 카테고리

일반 설명

Ammonium formate is the ammonium salt of formic acid. It is readily available, is stable and nontoxic in nature. It can be used in conjugation with Palladium on carbon (Pd-C) or Raney-Nickel catalysts.

애플리케이션

Ammonium formate has been used as buffer solution during LC-MS/MS analysis for screening of drugs and exogenous compounds. It may be used as a catalytic hydrogen transfer agent in reduction of aliphatic and aromatic nitro compounds.
Ammonium formate has been used in the separation of non-steroidal anti-inflammatory drugs and of oligosaccharide mixtures using capillary electrochromatography. It is also used in the analysis of phosphatidylserines, triacylglycerols and triacylglycerol oxidation products, and oligogalacturonic acids using HPLC and HPLC-MS methods.
Ammonium formate has been used as buffer solution during LC-MS/MS analysis for screening of drugs and exogenous compounds. It may be used as a catalytic hydrogen transfer agent in reduction of aliphatic and aromatic nitro compounds.

법적 정보

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

픽토그램

Exclamation mark
GHS07

신호어

Warning

유해 및 위험 성명서

H319

Hazard Classifications

Eye Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

dust mask type N95 (US), Eyeshields, Gloves

가장 최신 버전 중 하나를 선택하세요:

시험 성적서(COA)

Lot/Batch Number
0000194531
BCCG7486
BCCG2341
BCCF3910
BCCD3960

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특정 버전이 필요한 경우 로트 번호나 배치 번호로 특정 인증서를 찾을 수 있습니다.

COA 검색

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문서 라이브러리에서 최근에 구매한 제품에 대한 문서를 찾아보세요.

문서 라이브러리 방문

A general procedure for mild and rapid reduction of aliphatic and aromatic nitro compounds using ammonium formate as a catalytic hydrogen transfer agent.
Ram, Siya, and Richard E. Ehrenkaufer.
Tetrahedron Letters, 25.32, 3415-3418 (1984)
François-Ludovic Sauvage et al.
Clinical chemistry, 52(9), 1735-1742 (2006-07-22)
In clinical and forensic toxicology, general unknown screening is used to detect and identify exogenous compounds. In this study, we aimed to develop a comprehensive general unknown screening method based on liquid chromatography coupled with a hybrid triple-quadrupole linear ion
Satu Hänninen et al.
Bio-protocol, 7(9), e2268-e2268 (2017-05-05)
Glycerophospholipids consist of a glycerophosphate backbone to which are esterified two acyl chains and a polar head group. The head group (e.g., choline, ethanolamine, serine or inositol) defines the glycerophospholipid class, while the acyl chains together with the head group
Yajing Lv et al.
PLoS biology, 18(11), e3000872-e3000872 (2020-11-14)
Metabolic reprogramming to fulfill the biosynthetic and bioenergetic demands of cancer cells has aroused great interest in recent years. However, metabolic reprogramming for cancer metastasis has not been well elucidated. Here, we screened a subpopulation of breast cancer cells with
Anne M Filppula et al.
Drug metabolism and disposition: the biological fate of chemicals, 42(7), 1202-1209 (2014-04-10)
Previous studies have shown that several protein kinase inhibitors are time-dependent inhibitors of cytochrome P450 (CYP) 3A. We screened 14 kinase inhibitors for time-dependent inhibition of CYP2C8 and CYP3A. Amodiaquine N-deethylation and midazolam 1'-hydroxylation were used as marker reactions for
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