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Chemical substance record

Cyprodinil

121552-61-2C14H15N3225.295 g/mol

A member of the class of aminopyrimidine that is N-phenylpyrimidin-2-amine carrying additional cyclopropyl and methyl substituents at positions 4 and 6 respectively. A broad spectrum fungicide used to control a range of pathogens including Tapesia yallundae, Botrytis spp., Alternaria spp. and Rhynchospium secalis. Whilst it is a recognised irritant no serious human health concerns have been identified. It is moderately toxic to birds as well as most aquatic organisms and earthworms, but it is not considered toxic to honeybees. — ChEBI

Safety references

Safety documents & references

1 indexed references
JP · NITE

Government GHS classification

R03-C-120A-MOE · FY2021

View classification

Find a product-specific SDS

Safety guides and government classification records are not a manufacturer’s SDS. Match supplier, product number, concentration, physical form, region and revision before using a document.

Identity & molecular properties

Source-linked values
CAS number121552-61-2ChEBI ↗
Molecular formulaC14H15N3ChEBI ↗
Molar mass225.295 g/molChEBI ↗
Monoisotopic mass225.1266 DaChEBI ↗
Formal charge0ChEBI ↗
ChEBI identifierCHEBI:4045ChEBI ↗

Cross-source molecular data

PubChem
Molar mass225.29 g/molPubChem ↗
Exact mass225.126597491 DaPubChem ↗
Computed XLogP3.1PubChem ↗
Topological polar surface area (Ų)37.8PubChem ↗
H-bond donors1PubChem ↗
H-bond acceptors3PubChem ↗
Rotatable bonds3PubChem ↗

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
cyprodinil
4-cyclopropyl-6-methyl-N-phenylpyrimidin-2-amine
HAORKNGNJCEJBX-UHFFFAOYSA-N
Cc1cc(C2CC2)nc(Nc2ccccc2)n1
InChI=1S/C14H15N3/c1-10-9-13(11-7-8-11)17-14(15-10)16-12-5-3-2-4-6-12/h2-6,9,11H,7-8H2,1H3,(H,15,16,17)

Names & synonyms

4-cyclopropyl-6-methyl-N-phenylpyrimidin-2-amine

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

Classification & relationships

ChEBI ontology

Roles recorded in ChEBI

xenobioticaryl hydrocarbon receptor agonistenvironmental contaminantantifungal agrochemical

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

Safety classification · Japan

NITE / Japanese government
Japan · FY2021 source classification
4-Cyclopropyl-6-methyl-N-phenylpyrimidin-2-amine (synonym: Cyprodinil) · R03-C-120A-MOE
EndpointReported classification
Hazardous to the aquatic environment (Acute)Category 1
Hazardous to the aquatic environment (Long-term)Category 1

Selected source-reported endpoints. Other endpoints, rationales and conditions remain in the original classification. Missing or unlisted information does not mean non-hazardous. This is not a global classification or transport decision.

Read the original NITE classification

Mass ↔ amount of substance

Calculated from sourced mass
Equivalent amount
0.00443862 mol

Uses 225.295 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 · 14 atoms
74.64%
N
Nitrogen · 3 atoms
18.65%
H
Hydrogen · 15 atoms
6.71%

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
Cyprodinil as an activator of aryl hydrocarbon receptor. ↗Toxicology · 2013 Feb 8 · PMID 23228475
EP1023838 · Patent reference ↗Patent cross-reference supplied by ChEBI. Association alone does not establish claim scope.
US2011021580 · 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:4045

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

NCBI PubChem · CID 86367 · 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.