372331
Ammonium acetate
99.999% trace metals basis
동의어(들):
Ammonium ethanoate
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제품정보 (DICE 배송 시 비용 별도)
Linear Formula:
CH3CO2NH4
CAS 번호:
Molecular Weight:
77.08
NACRES:
NA.23
PubChem Substance ID:
eCl@ss:
39021908
UNSPSC Code:
12352302
EC Number:
211-162-9
MDL number:
Beilstein/REAXYS Number:
4186741
Assay:
99.999% trace metals basis
Form:
crystalline, solid
assay
99.999% trace metals basis
form
crystalline, solid
technique(s)
HPLC: suitable
impurities
≤20.0 ppm Trace Metal Analysis
mp
110-112 °C (dec.) (lit.)
SMILES string
N.CC(O)=O
InChI
1S/C2H4O2.H3N/c1-2(3)4;/h1H3,(H,3,4);1H3
InChI key
USFZMSVCRYTOJT-UHFFFAOYSA-N
General description
Ammonium acetate is a white crystalline water-soluble ammonium salt with unique properties that make it suitable for use in solar cells, batteries, and fuel cell catalysts.
Application
Ammonium acetate can be used:
- To passivate CsPbI3 perovskite nanocrystals for red LEDs. Ammonium acetate effectively eliminate undesired surface metallic lead cations and dangling bonds to enhance the stability and photoluminescence quantum yield (PLQY).
- As an additive to fabricate high quality perovskite solar cell with enhanced power conversion efficiency (PCE) of 13.9%. It promotes crystallization and improve performance without changing the perovskite composition.
- As a cost effective and green electrolyte for all-organic battery-supercapacitor hybrid device with maximum energy density.
- As an electrolyte additive for aqueous zinc batteries. It helps to improve cycling stability and capacity retention.
저장 등급
11 - Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
문서
Discover how elemental impurities affect API synthesis and how our ultra high purity salts and catalysts help overcome key contamination challenges.
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)