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Merck
모든 사진(1)

주요 문서

09689

Sigma-Aldrich

Ammonium acetate

BioUltra, for molecular biology, ≥99.0%

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About This Item

Linear Formula:
CH3CO2NH4
CAS Number:
Molecular Weight:
77.08
Beilstein:
4186741
EC Number:
MDL number:
UNSPSC 코드:
12352302
eCl@ss:
39021908
PubChem Substance ID:
NACRES:
NA.25

Grade

for molecular biology

Quality Level

제품 라인

BioUltra

분석

≥99.0% (calc. based on dry substance, T)
≥99.0%

형태

solid

불순물

insoluble matter, passes filter test
≤0.005% KMnO4-reducing substances
≤2% water

무기 잔류물

≤0.01% (as SO4)

pH

6.5-7.5 (25 °C, 1 M in H2O)

mp

110-112 °C (dec.) (lit.)

solubility

H2O: 1 M at 20 °C, clear, colorless

음이온 미량물

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

양이온 미량물

Al: ≤5 mg/kg
As: ≤0.1 mg/kg
Ba: ≤5 mg/kg
Bi: ≤5 mg/kg
Ca: ≤10 mg/kg
Cd: ≤5 mg/kg
Co: ≤5 mg/kg
Cr: ≤5 mg/kg
Cu: ≤5 mg/kg
Fe: ≤2 mg/kg
K: ≤50 mg/kg
Li: ≤5 mg/kg
Mg: ≤5 mg/kg
Mn: ≤5 mg/kg
Mo: ≤5 mg/kg
Na: ≤50 mg/kg
Ni: ≤5 mg/kg
Pb: ≤5 mg/kg
Sr: ≤5 mg/kg
Zn: ≤5 mg/kg

λ

1 M in H2O

UV 흡수

λ: 260 nm Amax: ≤0.015
λ: 280 nm Amax: ≤0.010

SMILES string

N.CC(O)=O

외래 활성

DNAse, none detected
Phosphatase, none detected
Protease, none detected
RNAse, none detected

InChI

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

InChI key

USFZMSVCRYTOJT-UHFFFAOYSA-N

유사한 제품을 찾으십니까? 방문 제품 비교 안내

애플리케이션


  • Modified QuEChERS method combined with ultra performance liquid chromatography-tandem mass spectrometry for detection of cyclopiazonic acid in feeds.: Ammonium acetate is utilized in a modified QuEChERS extraction method, improving the detection of mycotoxins in animal feed and contributing to agricultural safety and animal health (Peng et al., 2024).

  • Simultaneous determination of 31 banned veterinary drugs during egg-laying period in poultry eggs by ultra performance liquid chromatography-tandem mass spectrometry.: Highlights the role of ammonium acetate in a sensitive analytical method for monitoring drug residues in poultry eggs, crucial for food safety and consumer protection (Zhu et al., 2024).

  • Evaluation of diethyl 4-(5-bromo-1H-indol-3-yl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate: synthesis, anti-corrosion potential, and biomedical applications.: Discusses the use of ammonium acetate in the synthesis and evaluation of novel compounds with applications in materials science and medicine, showcasing its versatility in chemical synthesis (Ahamed et al., 2024).

  • Copper(II)/polyimide linked covalent organic framework as a powerful catalyst for the solvent-free microwave irradiation-based synthesis of 2,4,5-trisubstituted imidazoles.: Features the application of ammonium acetate in the development of advanced catalytic systems for green chemistry, promoting sustainable manufacturing processes (Sedaghat et al., 2023).

생화학적/생리학적 작용

Ammonium acetate can be used in x-ray crystallography, optimization reagents, protein structural analysis, and proteomics. It can also be used in a study to develop a novel and simple high-performance liquid chromatography (HPLC) method for the simultaneous determination of two selective serotonin reuptake inhibitors and two serotonin-norepinephrine reuptake inhibitors in alternative samples of toxicological interest such as hair, nail clippings, and cerebrospinal fluid.

기타 정보

Elution buffer in separation of proteins by gel filtration, ammonium acetate is volatile and can be removed during lyophilization.

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

Eyeshields, Gloves, type N95 (US)


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문서 라이브러리 방문

C.W. Hirs
Methods in Enzymology, 47, 105-105 (1977)
Jessica Z Bereszczak et al.
Protein science : a publication of the Protein Society, 23(7), 884-896 (2014-04-10)
Hepatitis B virus core-antigen (capsid protein) and e-antigen (an immune regulator) have almost complete sequence identity, yet the dimeric proteins (termed Cp149d and Cp(-10)149d , respectively) adopt quite distinct quaternary structures. Here we use hydrogen deuterium exchange-mass spectrometry (HDX-MS) to
Elena N Kitova et al.
Journal of the American Society for Mass Spectrometry, 25(11), 1908-1916 (2014-08-20)
A semiquantitative electrospray ionization mass spectrometry (ESI-MS) binding assay suitable for analyzing mixtures of oligosaccharides, at unknown concentrations, for interactions with target proteins is described. The assay relies on the differences in the ratio of the relative abundances of the
Hong Lin et al.
Journal of the American Society for Mass Spectrometry, 23(12), 2122-2131 (2012-09-21)
Electrospray ionization mass spectrometry (ESI-MS) measurements were performed under a variety of solution conditions on a highly acidic sub-fragment (B3C) of the C-terminal carbohydrate-binding repeat region of Clostridium difficile toxin B, and two mutants (B4A and B4B) containing fewer acidic
Xumin Zhang et al.
Analytical chemistry, 84(18), 7785-7792 (2012-08-15)
Untargeted liquid chromatography-mass spectrometry (LC-MS)-based metabolomics studies are usually carried out in both positive and negative ion modes; however, it is frequently ignored that the optimal conditions in positive ion mode and negative ion mode are often not the same.

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