Dicyandiamide（DCD） - ≥99% , CAS No.461-58-5

CAS: 461-58-5 Cat. No.: D100426 Formula: C₂H₄N₄ Molecular Weight: 84.08 Beilstein Registry Number: 605637 EC Number: 207-312-8

GRADE & PURITY ≥99%

Synonyms

3-cyanoguanidine | AKOS000118777 | ACR-H 3636 | EN300-21430 | Araldite XB 2979B | Dicyanadiamide | DTXSID1020354 | Z203045078 | Metformin impurity A, European Pharmacopoeia (EP) Reference Standard | Pyroset DO | CCRIS 3478 | Guanidine-1-carbonitrile | AKO

Storage

Store at 2-8°C,Protected from light

Shipped In

Wet ice

Overview

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.

Product Application：

Dicyandiamide is used in the synthesis of barbiturates. It is used as a stabilizer of ammonium dinitramide melt. It is used as hardener.
Dicyandiamide can be used as an organic precursor for synthesizing carbon nitride nanosheets. 

Specifications

Synonyms

3-cyanoguanidine | AKOS000118777 | ACR-H 3636 | EN300-21430 | Araldite XB 2979B | Dicyanadiamide | DTXSID1020354 | Z203045078 | Metformin impurity A, European Pharmacopoeia (EP) Reference Standard | Pyroset DO | CCRIS 3478 | Guanidine-1-carbonitrile | AKO

Specifications & Purity

≥99%

Storage

Store at 2-8°C,Protected from light

Shipped In

Wet ice

This product requires cold chain shipping. Ground and other economy services are not available.

Purity

≥99%

Names and Identifiers

Pubchem Sid

508812180

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/508812180

Canonical Smiles

C(#N)N=C(N)N

IUPAC Name

2-cyanoguanidine

InChIKey

QGBSISYHAICWAH-UHFFFAOYSA-N

INCHI

1S/C2H4N4/c3-1-6-2(4)5/h(H4,4,5,6)

Isomeric SMILES

C(#N)N=C(N)N

WGK Germany

1

RTECS

ME9950000

Molecular Weight

84.08

Beilstein

605637

Reaxy-Rn

1700035

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1700035&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic nitrogen compounds
    • Class Organonitrogen compounds
      • Subclass Guanidines

• Kingdom: Organic compounds
• Superclass: Organic nitrogen compounds
• Class: Organonitrogen compounds
• Subclass: Guanidines
• Intermediate Tree Nodes: Not available
• Direct Parent: Guanidines
• Alternative Parents: Propargyl-type 1,3-dipolar organic compounds Carboximidamides Organopnictogen compounds Imines Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Guanidine - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Carboximidamide - Organopnictogen compound - Hydrocarbon derivative - Imine - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as guanidines. These are compounds containing a guanidine moiety, with the general structure (R1R2N)(R3R4N)C=N-R5.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Mechanisms of Action

Chemical and Physical Properties

• Solubility: Soluble in Water: 0.1 g/mL
• Sensitivity: Moisture sensitive.
• Melt Point(°C): 208-211°C
• Molecular Weight: 84.080 g/mol
• XLogP3: -1.200
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 0
• Exact Mass: 84.0436 Da
• Monoisotopic Mass: 84.0436 Da
• Topological Polar Surface Area: 88.200 Ų
• Heavy Atom Count: 6
• Formal Charge: 0
• Complexity: 100.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1