1.01115
Ammonium acetate
EMPLURA®
Synonyme(s) :
Ammonium acetate
About This Item
Produits recommandés
Niveau de qualité
Gamme de produits
EMPLURA®
Pureté
≥96.0% (alkalimetric)
Forme
solid
Résidus de calcination
≤0.02% (as sulfate)
pH
6.7-7.3 (25 °C, 50 g/L in H2O)
Pf
114 °C
Solubilité
1480 g/L
Densité
1.17 g/cm3 at 20 °C
Masse volumique apparente
410 kg/m3
Traces d'anions
chloride (Cl-): ≤0.002%
sulfate (SO42-): ≤0.01%
Traces de cations
Fe: ≤0.001%
heavy metals (as Pb): ≤0.0005%
Température de stockage
15-25°C
InChI
1S/C2H4O2.H3N/c1-2(3)4;/h1H3,(H,3,4);1H3
Clé InChI
USFZMSVCRYTOJT-UHFFFAOYSA-N
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Catégories apparentées
Application
- 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).
Remarque sur l'analyse
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 %
Informations légales
Code de la classe de stockage
11 - Combustible Solids
Classe de danger pour l'eau (WGK)
WGK 1
Point d'éclair (°F)
Not applicable
Point d'éclair (°C)
Not applicable
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