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Merck
CN

V001100

Ammonium formate

96%

Synonym(s):

Formic acid ammonium salt

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About This Item

Linear Formula:
HCO2NH4
CAS Number:
Molecular Weight:
63.06
EC Number:
208-753-9
UNSPSC Code:
12352300
PubChem Substance ID:
Beilstein/REAXYS Number:
3625095
MDL number:
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InChI key

VZTDIZULWFCMLS-UHFFFAOYSA-N

InChI

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

SMILES string

N.OC=O

assay

96%

mp

119-121 °C (lit.)

density

1.26 g/mL at 25 °C (lit.)

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pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Eye Irrit. 2

Storage Class

11 - Combustible Solids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

Regulatory Information

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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
Todd A Lydic et al.
Methods (San Diego, Calif.), 87, 83-95 (2015-04-25)
There is an increasing recognition of the role that cancer cell derived exosomes play in intercellular signaling upon fusion or uptake with a target cell, including immune system evasion, tumor growth and metastasis. To date, however, although exosomal membrane and
Lucie Nováková et al.
Analytica chimica acta, 853, 647-659 (2014-12-04)
The potential and applicability of UHPSFC-MS/MS for anti-doping screening in urine samples were tested for the first time. For this purpose, a group of 110 doping agents with diverse physicochemical properties was analyzed using two separation techniques, namely UHPLC-MS/MS and
Jane Kilcoyne et al.
Journal of agricultural and food chemistry, 63(20), 5083-5091 (2015-04-25)
Azaspiracids (AZAs) are marine biotoxins produced by dinoflagellates that can accumulate in shellfish, which if consumed can lead to poisoning events. AZA7-10, 7-10, were isolated from shellfish and their structures, previously proposed on the basis of only LC-MS/MS data, were
Lucie Nováková et al.
Analytica chimica acta, 853, 637-646 (2014-12-04)
The conditions for the analysis of selected doping substances by UHPSFC-MS/MS were optimized to ensure suitable peak shapes and maximized MS responses. A representative mixture of 31 acidic and basic doping agents was analyzed, in both ESI+ and ESI- modes.

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