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About This Item
Linear Formula:
NH2C(=NH)NHCN
CAS Number:
Molecular Weight:
84.08
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
207-312-8
Beilstein/REAXYS Number:
605637
MDL number:
Product Name
Dicyandiamide, 99%
InChI key
QGBSISYHAICWAH-UHFFFAOYSA-N
InChI
1S/C2H4N4/c3-1-6-2(4)5/h(H4,4,5,6)
SMILES string
NC(=N)NC#N
assay
99%
form
powder
mp
208-211 °C (lit.)
Quality Level
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Application
Dicyandiamide can be used as an organic precursor for synthesizing carbon nitride nanosheets.
General description
Dicyandiamide is commonly used for the curing of epoxy resins. It is a nitrification inhibitor that is said to be capable of reducing nitrate (NO3-) leaching and nitrous oxide (N2O) emissions from grazed pasture soils.
Storage Class
11 - Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Rafał Olchowski et al.
Materials (Basel, Switzerland), 13(7) (2020-04-05)
Ordered mesoporous carbon (CMK-3), obtained from an abundant natural source, sugar, was thermochemically modified with dicyandiamide and thiourea as well as by classical oxidization with hydrogen peroxide to introduce specific surface groups. Thermochemical modifications resulted in carbon with almost unchanged
Ian Levett et al.
Journal of agricultural and food chemistry, 67(9), 2449-2458 (2019-02-07)
Dicyandiamide (DCD) has been studied as a stabilizer for nitrogen fertilizers for over 50 years. Its efficacy is limited at elevated temperatures, but this could be addressed by encapsulation to delay exposure. Here, poly(3-hydroxybutyrate- co-3-hydroxyvalerate) (PHBV) was investigated as a
The use of a nitrification inhibitor, dicyandiamide (DCD), to decrease nitrate leaching and nitrous oxide emissions in a simulated grazed and irrigated grassland.
Di HJ
Soil use and management, 18(4), 395-403 (2002)
Mette K Christensen et al.
Journal of medicinal chemistry, 56(22), 9071-9088 (2013-10-30)
Existing pharmacological inhibitors for nicotinamide phosphoribosyltransferase (NAMPT) are promising therapeutics for treating cancer. By using medicinal and computational chemistry methods, the structure-activity relationship for novel classes of NAMPT inhibitors is described, and the compounds are optimized. Compounds are designed inspired
Ming Hu et al.
Chemical communications (Cambridge, England), 47(28), 8124-8126 (2011-06-22)
We report a new synthetic route for preparation of nanoporous carbon nitride fibers with graphitic carbon nitride polymers, by calcination of Al-based porous coordination polymers (Al-PCPs) with dicyandiamide (DCDA) under a nitrogen atmosphere.
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