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Chemical substance record

Amitraz

33089-61-1C19H23N3293.414 g/mol

A tertiary amino compound that is 1,3,5-triazapenta-1,4-diene substituted by a methyl group at position 3 and 2,4-dimethylphenyl groups at positions 1 and 5. — ChEBI

Safety references

Safety documents & references

1 indexed references
JP · NITE

Government GHS classification

R02-B-103-MHLW, MOE · FY2020

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 number33089-61-1ChEBI ↗
Molecular formulaC19H23N3ChEBI ↗
Molar mass293.414 g/molChEBI ↗
Monoisotopic mass293.1892 DaChEBI ↗
Formal charge0ChEBI ↗
ChEBI identifierCHEBI:2665ChEBI ↗

Cross-source molecular data

PubChem
Molar mass293.4 g/molPubChem ↗
Exact mass293.189197746 DaPubChem ↗
Computed XLogP5.5PubChem ↗
Topological polar surface area (Ų)28PubChem ↗
H-bond donors0PubChem ↗
H-bond acceptors2PubChem ↗
Rotatable bonds4PubChem ↗

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

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amitraz
N'-(2,4-dimethylphenyl)-N-{[(2,4-dimethylphenyl)imino]methyl}-N-methylmethanimidamide
QXAITBQSYVNQDR-UHFFFAOYSA-N
[H]C(=Nc1ccc(C)cc1C)N(C)C([H])=Nc1ccc(C)cc1C
InChI=1S/C19H23N3/c1-14-6-8-18(16(3)10-14)20-12-22(5)13-21-19-9-7-15(2)11-17(19)4/h6-13H,1-5H3

Names & synonyms

amitrazumN'-(2,4-dimethylphenyl)-N-{[(2,4-dimethylphenyl)imino]methyl}-N-methylmethanimidamide

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

Classification & relationships

ChEBI ontology

Roles recorded in ChEBI

acaricideinsecticidexenobioticenvironmental contaminant

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 · FY2020 source classification
3-methyl-1,5-di(2,4-xylyl)-1,3,5-triazapenta-1,4-diene; Amitraz · R02-B-103-MHLW, MOE
EndpointReported classification
Acute toxicity (Oral)Category 4
Skin sensitizationCategory 1
CarcinogenicityCategory 2
Reproductive toxicityCategory 2, Additional category for effects on or via lactation
Specific target organ toxicity - Single exposureCategory 1 (nervous system), Category 3 (narcotic effects)
Specific target organ toxicity - Repeated exposureCategory 1 (central nervous system, liver)

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
0.00340815 mol

Uses 293.414 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 · 19 atoms
77.78%
N
Nitrogen · 3 atoms
14.32%
H
Hydrogen · 23 atoms
7.90%

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
Residues of amitraz, a new acaricide, on tea. ↗Bulletin of environmental contamination and toxicology · 2000 Aug · PMID 10885999
Intravenous amitraz poisoning. ↗Clinical toxicology (Philadelphia, Pa.) · 2005 · PMID 15822764

Sources & record history

Checked 27 Sep 2026
EMBL-EBI ChEBI · CHEBI:2665

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

NCBI PubChem · CID 36324 · 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.