292834
Ammonium carbamate
99%
Sinónimos:
Carbamic acid ammonium salt
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Fórmula lineal:
H2NCO2NH4
Número CAS:
Peso molecular:
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
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Permítanos ayudarleInChI key
BVCZEBOGSOYJJT-UHFFFAOYSA-N
InChI
1S/CH3NO2.H3N/c2-1(3)4;/h2H2,(H,3,4);1H3
SMILES string
[H]N([H])[H].NC(O)=O
vapor pressure
100 mmHg ( 26.7 °C)
assay
99%
form
powder or chunks
expl. lim.
2 %
storage temp.
2-8°C
Quality Level
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Categorías relacionadas
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).
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Skin Irrit. 2
Clase de almacenamiento
11 - Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Jo Sing Julia Tang et al.
Molecules (Basel, Switzerland), 25(21) (2020-11-08)
Glycans carry a vast range of functions in nature. Utilizing their properties and functions in form of polymers, coatings or glycan derivatives for various applications makes the synthesis of modified glycans crucial. Since amines are easy to modify for subsequent
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
William H Schaefer
Current drug metabolism, 7(8), 873-881 (2006-12-16)
Glucuronidation is an important mechanism used by mammalian systems to clear and eliminate both endogenous and foreign chemicals. Many functional groups are susceptible to conjugation with glucuronic acid, including hydroxyls, phenols, carboxyls, activated carbons, thiols, amines, and selenium. Primary and
An-Hua Liu et al.
Angewandte Chemie (International ed. in English), 51(45), 11306-11310 (2012-10-09)
Steric bulk controls CO(2) absorption: N-substituted amino acid salts in poly(ethylene glycol) reversibly absorb CO(2) in nearly 1:1 stoichiometry. Carbamic acid is thought to be the absorbed form of CO(2); this was supported by NMR and in situ IR spectroscopy
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