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Merck

32301-M

Sigma-Aldrich

Ammoniumacetat

puriss. p.a., ACS reagent, reag. Ph. Eur., ≥98%

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About This Item

Lineare Formel:
CH3CO2NH4
CAS-Nummer:
Molekulargewicht:
77.08
Beilstein:
4186741
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352300
eCl@ss:
39021908
PubChem Substanz-ID:
NACRES:
NA.21

Qualität

ACS reagent
puriss. p.a.

Qualitätsniveau

Agentur

reag. Ph. Eur.

Dampfdruck

<0.001 hPa

Assay

≥98%

Form

solid

Verunreinigungen

≤0.0002% heavy metals (as Pb)
≤0.005% KMnO4 red. matter (as HCOOH)
≤2% water (Karl Fischer)

Glührückstand

≤0.01% (as SO4)

pH-Wert

6.5-7.5 (25 °C, 77.1 g/L)

mp (Schmelzpunkt)

110-112 °C (dec.) (lit.)

Anionenspuren

chloride (Cl-): ≤5 mg/kg
nitrate (NO3-): ≤10 mg/kg
sulfate (SO42-): ≤10 mg/kg

Kationenspuren

Ca: ≤10 ppm
Cd: ≤2 ppm
Co: ≤5 ppm
Cr: ≤5 ppm
Cu: ≤2 ppm
Fe: ≤2 ppm
K: ≤50 ppm
Mg: ≤2 ppm
Mn: ≤5 ppm
Na: ≤50 ppm
Ni: ≤5 ppm
Pb: ≤2 ppm
Zn: ≤2 ppm

SMILES String

N.CC(O)=O

InChI

1S/C2H4O2.H3N/c1-2(3)4;/h1H3,(H,3,4);1H3

InChIKey

USFZMSVCRYTOJT-UHFFFAOYSA-N

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Allgemeine Beschreibung

Ammonium acetate is a colorless hygroscopic solid. It can be prepared by reacting glacial acetic acid with ammonia or ammonium carbonate. It has been reported as potential inhibitor of Pd/C mediated hydrogenolysis of benzyl ether.

Anwendung

Ammonium acetate has been used in the mobile phase for the HPLC determination of ezetimibe and its metabolites. It may be used in preparation of phenanthrimidazoles and retinimidazoles.

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 1

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable


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Die Dokumentenbibliothek aufrufen

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
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)
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)

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