1.01115
Ammonium acetate
EMPLURA®
Sinônimo(s):
Ammonium acetate
About This Item
Produtos recomendados
Nível de qualidade
linha de produto
EMPLURA®
Ensaio
≥96.0% (alkalimetric)
forma
solid
resíduo de ignição
≤0.02% (as sulfate)
pH
6.7-7.3 (25 °C, 50 g/L in H2O)
pf
114 °C
solubilidade
1480 g/L
densidade
1.17 g/cm3 at 20 °C
densidade volumétrica
410 kg/m3
traços de ânion
chloride (Cl-): ≤0.002%
sulfate (SO42-): ≤0.01%
traços de cátion
Fe: ≤0.001%
heavy metals (as Pb): ≤0.0005%
temperatura de armazenamento
15-25°C
InChI
1S/C2H4O2.H3N/c1-2(3)4;/h1H3,(H,3,4);1H3
chave InChI
USFZMSVCRYTOJT-UHFFFAOYSA-N
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Categorias relacionadas
Aplicação
- One-Pot, Four-Component Reaction for the Design, Synthesis, and SAR Studies of Novel Pyridines for Insecticidal Bioefficacy Screening against Cowpea Aphid (Aphis craccivora): This study explores the application of ammonium acetate in facilitating the synthesis of novel pyridine derivatives, evaluated for their insecticidal properties against Aphis craccivora (Alkorbi et al., 2024).
- A green analytical method for the simultaneous determination of 17 perfluoroalkyl substances (PFAS) in human serum and semen by ultra-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS): This research demonstrates the use of ammonium acetate in UPLC-MS/MS for detecting PFAS in biological samples, highlighting its role in environmental and health-related analytical chemistry (Di Giorgi et al., 2024).
- Innovation of 6-sulfonamide-2H-chromene derivatives as antidiabetic agents targeting α-amylase, α-glycosidase, and PPAR-γ inhibitors with in silico molecular docking simulation: Ammonium acetate was utilized in the synthesis process of new chromene derivatives, showing potential as antidiabetic agents by inhibiting α-amylase and α-glycosidase activities (Thabet et al., 2024).
- Regulation of Tetramethylpyrazine Formation by the Phenolics-Fenton Coupled Redox Cycling System: This article presents a study on the role of ammonium acetate in the formation of tetramethylpyrazine via redox cycling, an important reaction in food chemistry and possibly in synthesizing complex organic molecules (Xu et al., 2024).
- Simultaneous determination of unecritinib (TQ-B3101) and its active metabolite crizotinib in rat plasma by LC-MS/MS: An application to pharmacokinetic studies: This paper details the use of ammonium acetate in enhancing LC-MS/MS methodologies for pharmacokinetic studies, exemplifying its critical role in the analysis of pharmaceutical compounds (Wang et al., 2024).
Nota de análise
Identity: passes test
pH-value (5 %; water): 6.0 - 7.5
Chloride (Cl): ≤ 0.002 %
Sulfate (SO₄): ≤ 0.01 %
Heavy metals (as Pb): ≤ 0.0005 %
Fe (Iron): ≤ 0.001 %
Residue on ignition (as sulfate): ≤ 0.02 %
Water: ≤ 2.5 %
Informações legais
Código de classe de armazenamento
11 - Combustible Solids
Classe de risco de água (WGK)
WGK 1
Ponto de fulgor (°F)
Not applicable
Ponto de fulgor (°C)
Not applicable
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