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Key Documents

187364

Sigma-Aldrich

Cyanamide

99%

Sinonimo/i:

Carbimide, Hydrogen cyanamide

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About This Item

Formula condensata:
NCNH2
Numero CAS:
Peso molecolare:
42.04
Beilstein:
1732569
Numero CE:
Numero MDL:
Codice UNSPSC:
12352100
eCl@ss:
38060506
ID PubChem:
NACRES:
NA.22

Livello qualitativo

Saggio

99%

Forma fisica

crystals

contiene

stabilizer

P. eboll.

83 °C/0.5 mmHg (lit.)

Punto di fusione

45-46 °C (lit.)

Solubilità

ethanol: soluble 10%, clear to hazy, colorless to faintly yellow
water: soluble

Temperatura di conservazione

2-8°C

Stringa SMILE

NC#N

InChI

1S/CH2N2/c2-1-3/h2H2
XZMCDFZZKTWFGF-UHFFFAOYSA-N

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Descrizione generale

Cyanamide is an effective agent to treat alcoholism. Cyanamide in aqueous solution or in the form of its calcium salt is used as a fertilizer in agriculture. It is a potent inhibitor of liver aldehyde dehydrogenases in vivo.

Applicazioni

Cyanamide was used as nitrogen source in thermal transformation of metal oxide nanoparticles into nanocrystalline metal nitrides. It was used in the synthesis of mesoporous graphitic C3N4.

Avvertenze

Danger

Classi di pericolo

Acute Tox. 3 Dermal - Aquatic Chronic 3 - Carc. 2 - Eye Dam. 1 - Repr. 2 - Skin Corr. 1B - Skin Sens. 1 - STOT RE 2

Organi bersaglio

Thyroid

Codice della classe di stoccaggio

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges


Certificati d'analisi (COA)

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U H Maier-Greiner et al.
Proceedings of the National Academy of Sciences of the United States of America, 88(10), 4260-4264 (1991-05-15)
A protein was purified from crude extracts of the soil fungus Myrothecium verrucaria by gel filtration and hydrophobic chromatography to homogeneity; this protein catalyzed the stoichiometric hydration of the fertilizer cyanamide to urea with high substrate specificity. This cyanamide hydratase
Inhibition of aldehyde dehydrogenase in brain and liver by cyanamide.
R A Deitrich et al.
Biochemical pharmacology, 25(24), 2733-2737 (1976-12-15)
Anand K Ganesan et al.
PLoS genetics, 4(12), e1000298-e1000298 (2008-12-06)
Melanin protects the skin and eyes from the harmful effects of UV irradiation, protects neural cells from toxic insults, and is required for sound conduction in the inner ear. Aberrant regulation of melanogenesis underlies skin disorders (melasma and vitiligo), neurologic
Thermal transformation of metal oxide nanoparticles into nanocrystalline metal nitrides using cyanamide and urea as nitrogen source.
Buha J, et al.
Chemistry of Materials, 19(14), 3499-3505 (2007)
Woong Kwon et al.
Polymers, 12(7) (2020-07-08)
This study investigates the detoxification properties of guanidinylated chitosan against chemical warfare agents and its application to the preparation of military protective clothing. Guanidinylated chitosan was synthesized by chitosan guanidinylation with cyanamide. The detoxification properties of the guanidinylated chitosan were

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