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Merck
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Documenti

292834

Sigma-Aldrich

Ammonium carbamate

99%

Sinonimo/i:

Carbamic acid ammonium salt

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About This Item

Formula condensata:
H2NCO2NH4
Numero CAS:
1111-78-0
Peso molecolare:
78.07
Beilstein:
3914091
Numero CE:
214-185-2
Numero MDL:
MFCD00013010
Codice UNSPSC:
12352302
eCl@ss:
39033203
ID PubChem:
24857613
NACRES:
NA.23

Tensione di vapore

100 mmHg ( 26.7 °C)

Saggio

99%

Forma fisica

powder or chunks

Limite di esplosione

2 %

Temperatura di conservazione

2-8°C

Stringa SMILE

[H]N([H])[H].NC(O)=O

InChI

1S/CH3NO2.H3N/c2-1(3)4;/h2H2,(H,3,4);1H3
BVCZEBOGSOYJJT-UHFFFAOYSA-N

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Categorie correlate

Applicazioni

  • 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).

Pittogrammi

CorrosionExclamation mark
GHS05,GHS07

Avvertenze

Danger

Indicazioni di pericolo

H302,H315,H318

Classi di pericolo

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

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves

Certificati d'analisi (COA)

Cerca il Certificati d'analisi (COA) digitando il numero di lotto/batch corrispondente. I numeri di lotto o di batch sono stampati sull'etichetta dei prodotti dopo la parola ‘Lotto’ o ‘Batch’.

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Sigma-Aldrich

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Sulfur

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Sigma-Aldrich

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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
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
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