32301
乙酸铵
puriss. p.a., ACS reagent, reag. Ph. Eur., ≥98%
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关于此项目
线性分子式:
CH3CO2NH4
化学文摘社编号:
分子量:
77.08
NACRES:
NA.21
PubChem Substance ID:
eCl@ss:
39021908
UNSPSC Code:
12352300
EC Number:
211-162-9
MDL number:
Beilstein/REAXYS Number:
4186741
Assay:
≥98%
Form:
solid
产品名称
乙酸铵, puriss. p.a., ACS reagent, reag. Ph. Eur., ≥98%
InChI key
USFZMSVCRYTOJT-UHFFFAOYSA-N
InChI
1S/C2H4O2.H3N/c1-2(3)4;/h1H3,(H,3,4);1H3
SMILES string
N.CC(O)=O
grade
ACS reagent
puriss. p.a.
agency
reag. Ph. Eur.
vapor pressure
<0.001 hPa
assay
≥98%
form
solid
impurities
≤0.005% KMnO4 red. matter (as O)
≤2% water (Karl Fischer)
≤5 mg/kg heavy metals (as Pb)
ign. residue
≤0.01%
pH
6.7-7.3 (25 °C, 5% in water)
mp
110-112 °C (dec.) (lit.)
anion traces
chloride (Cl-): ≤5 mg/kg
nitrate (NO3-): ≤10 mg/kg
sulfate (SO42-): ≤10 mg/kg
cation traces
Ca: ≤10 ppm
Cd: ≤2 ppm
Co: ≤5 ppm
Cr: ≤5 ppm
Cu: ≤2 ppm
Fe: ≤5 ppm
K: ≤50 ppm
Mg: ≤2 ppm
Mn: ≤5 ppm
Na: ≤50 ppm
Ni: ≤5 ppm
Pb: ≤2 ppm
Zn: ≤2 ppm
Quality Level
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Application
在流动相中使用乙酸铵 HPLC 法测定 e zetimibe 及其代谢产物。它可用于制备苯并噻啶唑和维甲胺唑。
General description
乙酸铵为无色吸湿性固体。可由冰醋酸与氨水或碳酸铵反应制得。它是 Pd/C 催化苄基醚氢解反应的潜在抑制剂。
存储类别
11 - Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
Anima Ghosal et al.
Drug metabolism and disposition: the biological fate of chemicals, 32(3), 314-320 (2004-02-24)
Ezetimibe [1-(4-fluorophenyl)-3(R)-[3-(4-fluorophenyl)-3(S)-hydroxypropyl]-4(S)-(4-hydroxyphenyl)-2-azetidinone] (Zetia; Schering-Plough, Kenilworth, NJ) is the first in a new class of cholesterol-lowering agents known as cholesterol absorption inhibitors. The objective of this study was to identify the isoform(s) of human liver and intestinal UDP-glucuronosyltransferase (UGT) enzymes responsible
Selective inhibition of benzyl ether hydrogenolysis with Pd/C due to the presence of ammonia, pyridine or ammonium acetate.
Sajiki H.
Tetrahedron Letters, 36(20), 3465-3468 (1995)
Reactions of phenanthraquinone and retenequinone with aldehydes and ammonium acetate in acetic acid solution1.
Steck EA and Day AR.
Journal of the American Chemical Society, 65(3), 452-456 (1943)
M Athar Masood et al.
Basic & clinical pharmacology & toxicology, 127(6), 533-550 (2020-11-03)
Urine drug testing (UDT) is an important analytical/bio-analytical technique that has inevitably become an integral and vital part of a testing programme for diagnostic purposes. This manuscript presents a tailor-made LC-MS/MS quantitative assay method development and validation for a custom
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