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Sigma-Aldrich

Ammonium carbamate

99%

Synonym(s):

Carbamic acid ammonium salt

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About This Item

Linear Formula:
H2NCO2NH4
CAS Number:
1111-78-0
Molecular Weight:
78.07
Beilstein/REAXYS Number:
3914091
EC Number:
214-185-2
MDL number:
MFCD00013010
UNSPSC Code:
12352302
eCl@ss:
39033203
PubChem Substance ID:
24857613
NACRES:
NA.23

vapor pressure

100 mmHg ( 26.7 °C)

assay

99%

form

powder or chunks

expl. lim.

2 %

storage temp.

2-8°C

SMILES string

[H]N([H])[H].NC(O)=O

InChI

1S/CH3NO2.H3N/c2-1(3)4;/h2H2,(H,3,4);1H3

InChI key

BVCZEBOGSOYJJT-UHFFFAOYSA-N

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application

  • Cooperative Carbon Dioxide Capture in Diamine-Appended Magnesium-Olsalazine Frameworks.: This article discusses a novel method for carbon dioxide capture using diamine-appended frameworks, where ammonium carbamate serves as a key chemical intermediate. This research underscores the environmental benefits of using ammonium carbamate in carbon capture technologies, contributing to efforts to mitigate climate change (Zhu et al., 2023).

pictograms

CorrosionExclamation mark
GHS05,GHS07

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Skin Irrit. 2

Storage Class

11 - Combustible Solids

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Environmental science & technology, 47(2), 1163-1169 (2012-11-30)
The present study reports (a) the determination of both the kinetic rate constants and equilibrium constants for the reaction of CO(2)(aq) with sterically hindered amines and (b) an attempt to elucidate a fundamental chemical understanding of the relationship between the
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The journal of physical chemistry. A, 113(9), 1858-1863 (2009-02-13)
A procedure is described for the theoretical study of chemical reactions in solution by means of molecular dynamics simulation, with solute-solvent interaction potentials derived from ab initio quantum calculations. We apply the procedure to the case of neutral hydrogen isocyanate
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