Skip to Content
Merck
All Photos(1)

Key Documents

292834

Sigma-Aldrich

Ammonium carbamate

99%

Synonym(s):

Carbamic acid ammonium salt

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
H2NCO2NH4
CAS Number:
Molecular Weight:
78.07
Beilstein:
3914091
EC Number:
MDL number:
UNSPSC Code:
12352302
eCl@ss:
39033203
PubChem Substance ID:
NACRES:
NA.23

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

Looking for similar products? Visit Product Comparison Guide

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

Signal Word

Danger

Hazard Statements

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’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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
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
William Conway et al.
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
S Tolosa Arroyo et al.
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
J J McGrath et al.
Animal : an international journal of animal bioscience, 7(3), 404-409 (2012-10-23)
The influence of feeds containing varying dietary cation-anion differences (DCADs) with and without supplements of 25-hydroxyvitamin D (25(OH)D) on urine pH and excretion of macro minerals was determined in fistulated crossbred steers (mean live weight 315 ± 45 kg). A

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service