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C87908

Sigma-Aldrich

Cyanamide solution

50 wt. % in H2O

Synonym(s):

Alzogur, Amidocyanogen, Amino cyanide, Carbamonitrile, Carbimide

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About This Item

Linear Formula:
NCNH2
CAS Number:
420-04-2
Molecular Weight:
42.04
Beilstein:
1732569
MDL number:
MFCD00007572
UNSPSC Code:
12352100
PubChem Substance ID:
24893106
NACRES:
NA.22

form

liquid

concentration

50 wt. % in H2O

refractive index

n20/D 1.405

density

1.082 g/mL at 25 °C

storage temp.

2-8°C

SMILES string

NC#N

InChI

1S/CH2N2/c2-1-3/h2H2

InChI key

XZMCDFZZKTWFGF-UHFFFAOYSA-N

Signal Word

Danger

Hazard Classifications

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

Target Organs

Thyroid

Storage Class Code

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

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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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
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
Santiago Signorelli et al.
Journal of experimental botany, 71(2), 719-729 (2019-05-01)
The physiological constraints on bud burst in woody perennials, including vascular development and oxygenation, remain unresolved. Both light and tissue oxygen status have emerged as important cues for vascular development in other systems; however, grapevine buds have only a facultative
Hisayo Yamane et al.
Journal of experimental botany, 62(10), 3481-3488 (2011-03-08)
The present study investigated the expressional regulation of PpDAM5 and PpDAM6, two of the six peach (Prunus persica) dormancy-associated MADS-box genes, in relation to lateral bud endodormancy. PpDAM5 and PpDAM6 were originally identified as homologues of Arabidopsis SHORT VEGETATIVE PHASE/AGAMOUS-LIKE
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