Record Information
Version1.0
Creation Date2014-08-29 06:51:41 UTC
Update Date2026-08-23 04:15:17 UTC
Accession NumberCHEM003453
Identification
Common NameCyromazine
ClassSmall Molecule
Description
Ectoparasiticide. Insect growth regulator. Specific activity against dipterous larvae. Cyromazine is a fda approved for use in livestock. Cyromazine belongs to the family of Aminotriazines. These are organic compounds containing an amino group attached to a triazine ring.
Contaminant Sources
  • FooDB Chemicals
  • HPV EPA Chemicals
  • My Exposome Chemicals
  • STOFF IDENT Compounds
  • T3DB toxins
  • ToxCast & Tox21 Chemicals
Contaminant Type
  • Amine
  • Food Toxin
  • Metabolite
  • Organic Compound
  • Pesticide
  • Synthetic Compound
Chemical Structure
Synonyms
ValueSource
2,4-Diamino-6-(cyclopropylamino)-S-triazineChEBI
2-Cyclopropylamino-4,6-diamino-S-triazineChEBI
CyclopropylmelamineChEBI
LarvadexChEBI
N-Cyclopropyl-1,3,5-triazine-2,4,6-triamineChEBI
N-CyclopropylmelamineChEBI
TrigardChEBI
VetrazinChEBI
NeporexKegg
2,4-Diamino-6-(cyclopropylamino)-S-triazine (8ci)HMDB
ArmorHMDB
AzimethiphosHMDB
CGA 72662HMDB
CiromazinaHMDB
CitationHMDB
Cyclopropyl-1,3,5-triazine-2,4,6-triamineHMDB
CypromazineHMDB
CyromazinHMDB
CyromazinumHMDB
Diamino-6-(cyclopropylamino)-S-triazineHMDB
Larvadex premixHMDB
N(2)-Cyclopropyl-1,3,5-triazine-2,4,6-triamineHMDB
N-Cyclopropyl-1,3,5-triazin-2,4,6-triamineHMDB
N-Cyclopropyl-1,3,5-triazine-2,4,6-triamine, 9ciHMDB
N-Cyclopropyl-2,4,6-triamino-1,3,5-triazineHMDB
N-Cyclopropyltriazine-2,4,6-triamineHMDB
N2-Cyclopropyl-1,3,5-triazine-2,4,6-triamineHMDB
NeoprexHMDB
Vetrazin (pesticide)HMDB
VetrazineHMDB
Cyromazine dihydrochlorideHMDB
Chemical FormulaC6H10N6
Average Molecular Mass166.184 g/mol
Monoisotopic Mass166.097 g/mol
CAS Registry Number66215-27-8
IUPAC NameN2-cyclopropyl-1,3,5-triazine-2,4,6-triamine
Traditional Namecyromazine
SMILESNC1=NC(NC2CC2)=NC(N)=N1
InChI IdentifierInChI=1S/C6H10N6/c7-4-10-5(8)12-6(11-4)9-3-1-2-3/h3H,1-2H2,(H5,7,8,9,10,11,12)
InChI KeyLVQDKIWDGQRHTE-UHFFFAOYSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as n-aliphatic s-triazines. These are n-aliphatic amine derivatives of 1,3,5-triazines. 1,3,5-Triazines are aromatic compounds having three nitrogen ring atoms at the 1-, 3-, and 5- positions.
KingdomOrganic compounds
Super ClassOrganoheterocyclic compounds
ClassTriazines
Sub ClassAminotriazines
Direct ParentN-aliphatic s-triazines
Alternative Parents
Substituents
  • N-aliphatic s-triazine
  • Secondary aliphatic/aromatic amine
  • 1,3,5-triazine
  • Heteroaromatic compound
  • Azacycle
  • Secondary amine
  • Organic nitrogen compound
  • Organopnictogen compound
  • Hydrocarbon derivative
  • Primary amine
  • Organonitrogen compound
  • Amine
  • Aromatic heteromonocyclic compound
Molecular FrameworkAromatic heteromonocyclic compounds
External Descriptors
Biological Properties
StatusDetected and Not Quantified
OriginExogenous
Cellular Locations
  • Cytoplasm
  • Extracellular
Biofluid LocationsNot Available
Tissue LocationsNot Available
PathwaysNot Available
Applications
Biological RolesNot Available
Chemical RolesNot Available
Physical Properties
StateSolid
AppearanceWhite powder.
Experimental Properties
PropertyValue
Melting Point219 - 222°C
Boiling PointNot Available
SolubilityNot Available
Predicted Properties
PropertyValueSource
Water Solubility2.71 g/LALOGPS
logP0.04ALOGPS
logP0.17ChemAxon
logS-1.8ALOGPS
pKa (Strongest Acidic)14.86ChemAxon
pKa (Strongest Basic)8.36ChemAxon
Physiological Charge1ChemAxon
Hydrogen Acceptor Count6ChemAxon
Hydrogen Donor Count3ChemAxon
Polar Surface Area102.74 ŲChemAxon
Rotatable Bond Count2ChemAxon
Refractivity49.17 m³·mol⁻¹ChemAxon
Polarizability16.83 ųChemAxon
Number of Rings2ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterYesChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Spectra
Spectra
Toxicity Profile
Route of ExposureNot Available
Mechanism of ToxicityNot Available
MetabolismNot Available
Toxicity ValuesNot Available
Lethal DoseNot Available
Carcinogenicity (IARC Classification)No indication of carcinogenicity to humans (not listed by IARC).
Uses/SourcesThis is a man-made compound that is used as a pesticide.
Minimum Risk LevelNot Available
Health EffectsNot Available
SymptomsNot Available
TreatmentNot Available
Concentrations
Not Available
External Links
DrugBank IDNot Available
HMDB IDHMDB0029862
FooDB IDFDB001091
Phenol Explorer IDNot Available
KNApSAcK IDNot Available
BiGG IDNot Available
BioCyc IDNot Available
METLIN IDNot Available
PDB IDAX3
Wikipedia LinkCyromazine
Chemspider ID43550
ChEBI ID30260
PubChem Compound ID47866
Kegg Compound IDC14147
YMDB IDNot Available
ECMDB IDM2MDB004909
References
Synthesis ReferenceNot Available
MSDSNot Available
General References
1. Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.