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Merck

32301-M

Sigma-Aldrich

乙酸铵

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

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About This Item

线性分子式:
CH3CO2NH4
CAS号:
分子量:
77.08
Beilstein:
4186741
EC號碼:
MDL號碼:
分類程式碼代碼:
12352300
eCl@ss:
39021908
PubChem物質ID:
NACRES:
NA.21
化驗:
≥98%
形狀:
solid

等級

ACS reagent
puriss. p.a.

品質等級

agency

reag. Ph. Eur.

蒸汽壓力

<0.001 hPa

化驗

≥98%

形狀

solid

雜質

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

燃燒殘留物

≤0.01% (as SO4)

pH值

6.5-7.5 (25 °C, 77.1 g/L)

mp

110-112 °C (dec.) (lit.)

負離子痕跡

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

正離子痕跡

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 字串

N.CC(O)=O

InChI

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

InChI 密鑰

USFZMSVCRYTOJT-UHFFFAOYSA-N

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一般說明

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.

應用

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.

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 1

閃點(°F)

Not applicable

閃點(°C)

Not applicable


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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访问文档库

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)

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