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Merck

C87908

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:
Molecular Weight:
42.04
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
1732569
eCl@ss:
38060506
Form:
liquid
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InChI

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

SMILES string

NC#N

InChI key

XZMCDFZZKTWFGF-UHFFFAOYSA-N

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

Quality Level

signalword

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

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

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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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.
Yuewei Zhang et al.
Nanoscale, 4(17), 5300-5303 (2012-07-11)
Energy captured directly from sunlight provides an attractive approach towards fulfilling the need for green energy resources on the terawatt scale with minimal environmental impact. Collecting and storing solar energy into fuel through photocatalyzed water splitting to generate hydrogen in

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