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Chemical substance record

Dicyclanil

112636-83-6C8H10N6190.21 g/mol

A member of the class of aminopyrimidines that is pyrimidine-4,6-diamine substituted by cyclopropylamino and cyano groups at positions 2 and 5, respectively. It is an insect growth regulator that prevents blowfly strike in sheep. — ChEBI

Safety references

Safety documents & references

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Identity & molecular properties

Source-linked values
CAS number112636-83-6ChEBI ↗
Molecular formulaC8H10N6ChEBI ↗
Molar mass190.21 g/molChEBI ↗
Monoisotopic mass190.09669 DaChEBI ↗
Formal charge0ChEBI ↗
ChEBI identifierCHEBI:232105ChEBI ↗

Cross-source molecular data

PubChem
Molar mass190.21 g/molPubChem ↗
Exact mass190.09669434 DaPubChem ↗
Computed XLogP0.6PubChem ↗
Topological polar surface area (Ų)114PubChem ↗
H-bond donors3PubChem ↗
H-bond acceptors6PubChem ↗
Rotatable bonds2PubChem ↗

PubChem computed values are shown separately from the ChEBI record. An exact InChIKey match was used to connect the records. Molecular descriptors do not describe a supplied product’s purity, particle size or performance.

Names & structural identifiers

Copy any identifier
dicyclanil
4,6-diamino-2-(cyclopropylamino)pyrimidine-5-carbonitrile
PKTIFYGCWCQRSX-UHFFFAOYSA-N
N#Cc1c(N)nc(NC2CC2)nc1N
InChI=1S/C8H10N6/c9-3-5-6(10)13-8(14-7(5)11)12-4-1-2-4/h4H,1-2H2,(H5,10,11,12,13,14)

Names & synonyms

4,6-diamino-2-(cyclopropylamino)pyrimidine-5-carbonitrileCLiKZiN

Names are supplied by ChEBI. Trade names and related synonyms may describe a broader product context.

Classification & relationships

ChEBI ontology

Roles recorded in ChEBI

insect growth regulatorinsecticideantiparasitic agentcarcinogenic agent

Database role annotations describe reported biological or chemical roles; they are not product approvals or recommendations for use.

Mass ↔ amount of substance

Calculated from sourced mass
Equivalent amount
0.00525735 mol

Uses 190.21 g/mol from ChEBI. Assumes the substance described by this record; no purity or concentration correction is applied.

Elemental composition

Theoretical mass fractions
C
Carbon · 8 atoms
50.52%
N
Nitrogen · 6 atoms
44.18%
H
Hydrogen · 10 atoms
5.30%

Calculated theoretical mass fractions from the reported formula and PubChem periodic-table atomic masses. These are not assay or purity results.

Research & patent references

Selected source associations
Absence of in vivo genotoxicity and liver initiation activity of dicyclanil. ↗The Journal of toxicological sciences · 2003 Aug · PMID 12974609
WO2009118312 · Patent reference ↗Patent cross-reference supplied by ChEBI. Association alone does not establish claim scope.

Sources & record history

Checked 27 Sep 2026
EMBL-EBI ChEBI · CHEBI:232105

Release 255, 9 September 2026. ChEBI three-star (manually annotated) source entry. View original record ↗ · CC BY 4.0

NCBI PubChem · CID 3081364 · retrieved 2026-09-27

PubCAS formats source data, connects references and computes explicitly labelled conversions. CAS cross-references are supplied by ChEBI; they do not constitute CAS verification or endorsement.