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Sigma-Aldrich

Ammonium acetate

≥99.99% trace metals basis

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About This Item

Fórmula linear:
CH3CO2NH4
Número CAS:
Peso molecular:
77.08
Beilstein:
4186741
Número CE:
Número MDL:
Código UNSPSC:
12352300
eCl@ss:
39021908
ID de substância PubChem:

grau

for inorganic trace analysis

Nível de qualidade

Agency

suitable for ASTM® 7969
suitable for ASTM® 7979
suitable for DIN 38407-43
suitable for EPA 1634
suitable for EPA 534
suitable for EPA 538.1
suitable for EPA 8328
suitable for EPA ACB B21-03
suitable for EPA ACB B23-05b
suitable for GB 31604.35-2016
suitable for GB 5009.253-2016
suitable for ISO 21675 2019
suitable for ISO 25101
suitable for ISO/CEN 15968-2011

conformidade reg.

suitable for FDA C-010.02

pressão de vapor

<0.001 hPa

Ensaio

≥99.99% trace metals basis

forma

solid

Impurezas

≤0.005% insolubles
<100 ppm total metallic impurities

pH

6.7-7.3 (25 °C, 5% in water)
6.7-7.3

pf

110-112 °C (dec.) (lit.)

solubilidade

water: soluble 1,480 g/L at 4 °C

traços de ânion

chloride (Cl-): ≤5 ppm
nitrate (NO3-): ≤0.001%
sulfate (SO42-): ≤0.001%

traços de cátion

Fe: ≤5 ppm
heavy metals: ≤5 ppm

cadeia de caracteres SMILES

N.CC(O)=O

InChI

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

chave InChI

USFZMSVCRYTOJT-UHFFFAOYSA-N

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Descrição geral

Ammonium acetate (NH4C2H3O2) is water soluble, hygroscopic ammonium salt. It is ecofriendly and inexpensive, which can be prepared by reacting glacial acetic acid with ammonia or ammonium carbonate. It is commonly utilized in dye industry and as meat preservative. It participates in the generation of sol-gel formaldehyde sensors utilized for detecting formaldehyde in air samples. Neutron energy-gain spectrum of ammonium acetate has been recorded which gives data on the atomic motions. It has been reported to regenerate aldehydes from bisulfite addition products and diacetates in the absence of solvent and under microwave condition.
Meets ACS reagent specifications.

Aplicação

Ammonium acetate may be used as a component of mobile phase for HPLC analysis.
It may be used in the synthesis of the following:
  • Phenanthroline derivatives employed as corrosion inhibitors.
  • Highly substituted imidazoles.
  • 2,4-Diarylpolyhydroquinoline derivatives.

Informações legais

ASTM is a registered trademark of American Society for Testing and Materials

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


Certificados de análise (COA)

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Computational simulation and statistical analysis on the relationship between corrosion inhibition efficiency and molecular structure of some phenanthroline derivatives on mild steel surface.
Obi-Egbedi NO, et al.
International Journal of Electrochemical Science, 6, 5649-5675 (2011)
An eco-friendly regeneration of aldehydes exploiting ammonium acetate under microwave irradiation.
Mitra AK, et al.
J. Chem. Res. (M), 2004(3), 237-239 (2004)
DABCO as a mild and efficient catalytic system for the synthesis of highly substituted imidazoles via multi-component condensation strategy.
Murthy SN, et al.
Tetrahedron Letters, 51(40), 5252-5257 (2010)
Sol-gel based sensor for selective formaldehyde determination.
Bunkoed O, et al.
Analytica Chimica Acta, 659(1), 251-257 (2010)
Scattering of Cold Neutrons in Ammonium Carbonate, Ammonium Citrate, and Ammonium Acetate.
Myers VW.
J. Chem. Phys., 46(10), 4034-4035 (1967)

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