254134

Sigma-Aldrich

Ammonium chloride

99.998% trace metals basis

Synonym(s):
Salmiac
Linear Formula:
NH4Cl
CAS Number:
Molecular Weight:
53.49
Beilstein/REAXYS Number:
4371014
EC Number:
MDL number:
eCl@ss:
38050207
PubChem Substance ID:
NACRES:
NA.23

Quality Level

vapor density

1.9 (vs air)

vapor pressure

1 mmHg ( 160.4 °C)

assay

99.998% trace metals basis

form

powder

application(s)

HPLC: suitable

impurities

≤25.0  ppm Trace Metal Analysis

mp

340 °C (subl.) (lit.)

SMILES string

N.Cl

InChI

1S/ClH.H3N/h1H;1H3

InChI key

NLXLAEXVIDQMFP-UHFFFAOYSA-N

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Application

Ammonium chloride (NH4Cl) is an ammonium salt which can be used for a variety of applications such as:
  • a catalyst for the one-pot synthesis of 3,4-dihydropyrimidin-2-(1H)-ones
  • a promoter in the multicomponent synthesis of pyrrolo[3,4-b]pyridine-5-one
  • a reagent to improve the hydrolysis rate of magnesium hydride for the generation of hydrogen
  • a reductant, which facilitates the recovery of metals that are utilized in lithium-ion batteries

Packaging

5, 25, 100 g in poly bottle

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

hazcat

Acute Tox. 4 Oral - Eye Irrit. 2

storage_class_code

13 - Non Combustible Solids

WGK Germany

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US),Eyeshields,Gloves

Certificate of Analysis

Certificate of Origin

Ammonium chloride-promoted four-component synthesis of pyrrolo [3, 4-b] pyridin-5-one
Janvier P, et al.
Journal of the American Chemical Society, 124(11), 2560-2567 (2002)
A sustainable process for metal recycling from spent lithium-ion batteries using ammonium chloride
Lv W, et al.
Waste Management (New York, N.Y.), 79(18), 545-553 (2018)
Hydrogen generation by hydrolysis of MgH2 and enhanced kinetics performance of ammonium chloride introducing
Huang M, et al.
International Journal of Hydrogen Energy, 40(18), 6145-6150 (2015)
Ammonium chloride-catalyzed one-pot synthesis of 3,4-dihydropyrimidin-2-(1H)-ones under solvent-free conditions.
Shaabani A, et al.
Tetrahedron Letters, 44(4), 857-859 (2003)
Jackie Perrin et al.
Journal of cell science, 128(13), 2269-2277 (2015-05-23)
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