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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:
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

Signal Word

Danger

Hazard Statements

H302,H315,H318

Hazard Classifications

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

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Yoshiaki Miura et al.
Analytical chemistry, 82(24), 10021-10029 (2010-11-17)
Glycoblotting, high throughput method for N-glycan enrichment analysis based on the specific chemical ligation between aminooxy/hydrazide-polymers/solids and reducing N-glycans released from whole serum and cellular glycoproteins, was proved to be feasible for selective enrichment analysis of O-glycans of common (mucin)
Alexey P Ilyn et al.
The Journal of organic chemistry, 71(7), 2811-2819 (2006-03-25)
We present a convenient synthesis of novel heteroaryl-fused 3-oxo-1,4-thiazepine-5-carboxamides and 5-oxo-1,4-thiazepine-3-carboxamides using a modification of four-component Ugi condensation. We demonstrate the usefulness and versatility of the developed approach for the synthesis of variously substituted compounds and discuss the scope and
Akihiro Ohkubo et al.
Organic & biomolecular chemistry, 7(4), 687-694 (2009-02-06)
It was found that N-arylcarbamoyl and N-(phenylsulfonyl)carbamoyl (psc) groups could be effectively introduced onto the amino groups of deoxycytidine and deoxyadenosine derivatives and could be removed thermolytically. We succeeded in synthesizing DNA probes incorporating these thermo-removable protecting groups and developed
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