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C87908

Sigma-Aldrich

Cyanamide solution

50 wt. % in H2O

Sinonimo/i:

Alzogur, Amidocyanogen, Amino cyanide, Carbamonitrile, Carbimide

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About This Item

Formula condensata:
NCNH2
Numero CAS:
420-04-2
Peso molecolare:
42.04
Beilstein:
1732569
Numero MDL:
MFCD00007572
Codice UNSPSC:
12352100
ID PubChem:
24893106
NACRES:
NA.22
Prezzi e disponibilità al momento non sono disponibili

Stato

liquid

Concentrazione

50 wt. % in H2O

Indice di rifrazione

n20/D 1.405

Densità

1.082 g/mL at 25 °C

Temperatura di conservazione

2-8°C

Stringa SMILE

NC#N

InChI

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

Categorie correlate

Avvertenze

Danger

Classi di pericolo

Acute Tox. 3 Oral - Acute Tox. 4 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 ABEK (EN14387) respirator filter

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Certificati d'analisi (COA)

Lot/Batch Number
SDBB2949
STBL3536
STBL0340
STBK9350
STBK5369

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Yuan Liu et al.
Nanomaterials (Basel, Switzerland), 9(6) (2019-06-05)
To improve the power generation of a microbial fuel cell (MFC), a porous nitrogen-doped graphene/carbon black (NG/CB) composite as efficient oxygen reduction reaction (ORR) electrocatalyst was successfully synthesized by pyrolyzing graphene oxide (GO) encapsulated CB with cetyltrimethyl ammonium bromide as
Carmen Harb et al.
Inorganic chemistry, 52(3), 1621-1630 (2013-01-24)
Nine [Ru(Tp)(dppe)L] complexes, where Tp is hydrotris(pyrazol-1-yl)borate, dppe is ethylenebis(diphenylphosphine), and L is (4-nitrophenyl)cyanamide (NO(2)pcyd(-)), (2-chlorophenyl)cyanamide (2-Clpcyd(-)), (3-chlorophenyl)cyanamide (3-Clpcyd(-)), (2,4-dichlorophenyl)cyanamide (2,4-Cl(2)pcyd(-)), (2,3-dichlorophenyl)cyanamide (2,3-Cl(2)pcyd(-)), (2,5-dichlorophenyl)cyanamide (2,5-Cl(2)pcyd(-)), (2,4,5-trichlorophenyl)cyanamide (2,4,5-Cl(3)pcyd(-)), (2,3,5,6-tetrachlorophenyl)cyanamide (2,3,5,6-Cl(4)pcyd(-)), and (pentachlorophenyl)cyanamide (Cl(5)pcyd(-)), and the dinuclear complex [{Ru(Tp)(dppe)}(2)(μ-adpc)], where adpc(2-) is
Ricardo Vergara et al.
Plant molecular biology, 79(1-2), 171-178 (2012-04-03)
It has been reported that dormancy-breaking compound hydrogen cyanamide (HC) stimulates the fermentative pathway and inhibits respiration in grapevine-buds, suggesting in this way, that a respiratory stress must be involved in the release of buds from dormancy. Here, we tested
Cedric Maton et al.
Chemphyschem : a European journal of chemical physics and physical chemistry, 13(13), 3146-3157 (2012-06-26)
A versatile and efficient method to synthesize tetrasubstituted imidazoles via a one-pot modified Debus-Radziszewski reaction and their subsequent transformation into the corresponding imidazolium ionic liquids is reported. The tetrasubstituted imidazoles were also synthesized by means of a continuous flow process.
Dorota Soltys et al.
Planta, 234(3), 609-621 (2011-05-17)
Cyanamide is an allelochemical produced by hairy vetch (Vicia villosa Roth.). Its phyotoxic effect on plant growth was examined on roots of onion (Allium cepa L.) bulbs. Water solution of cyanamide (2-10 mM) restricted growth of onion roots in a
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