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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)

Quality Level

100

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)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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
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
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
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
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