D76609
Dicyandiamide
99%
Synonym(s):
DCD, Cyanoguanidine, Dicyanodiamide
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All Photos(3)
About This Item
Linear Formula:
NH2C(=NH)NHCN
CAS Number:
Molecular Weight:
84.08
Beilstein:
605637
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Assay
99%
form
powder
mp
208-211 °C (lit.)
SMILES string
NC(=N)NC#N
InChI
1S/C2H4N4/c3-1-6-2(4)5/h(H4,4,5,6)
InChI key
QGBSISYHAICWAH-UHFFFAOYSA-N
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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.
Application
Dicyandiamide can be used as an organic precursor for synthesizing carbon nitride nanosheets.
Storage Class Code
11 - Combustible Solids
WGK
WGK 1
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
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Customers Also Viewed
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
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.
Carbon nitride nanosheets for photocatalytic hydrogen evolution: remarkably enhanced activity by dye sensitization.
Wang Y
Catalysis Science & Technology, 3(7), 1703-1711 (2013)
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