292834
Ammonium carbamate
99%
Synonym(s):
Carbamic acid ammonium salt
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About This Item
Linear Formula:
H2NCO2NH4
CAS Number:
Molecular Weight:
78.07
NACRES:
NA.23
PubChem Substance ID:
eCl@ss:
39033203
UNSPSC Code:
12352302
EC Number:
214-185-2
MDL number:
Beilstein/REAXYS Number:
3914091
Assay:
99%
Form:
powder or chunks
vapor pressure
100 mmHg ( 26.7 °C)
Quality Level
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
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).
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signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Skin Irrit. 2
Storage Class
11 - Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
危险化学品
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Takayuki Furukawa et al.
Chembiochem : a European journal of chemical biology, 18(19), 1903-1909 (2017-08-06)
Although widely occurring lipid oxidation, which is triggered by reactive oxygen species (ROS), produces a variety of oxidized lipids, practical methods to efficiently analyze oxidized lipids remain elusive. Herein, it is shown that the glycoblotting platform can be used to
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
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)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 292834-25G | 04061826594742 |
| 292834-100G | 04061826594735 |
| 292834-500G | 04061826594759 |