Skip to content
[P]pubcas
Independent chemical reference Compare
Chemical substance record

Diphenylamine

122-39-4C12H11N169.227 g/mol

An aromatic amine containing two phenyl substituents. It has been used as a fungicide for the treatment of superficial scald in apples and pears, but is no longer approved for this purpose within the European Union. — ChEBI

Safety references

Safety documents & references

2 indexed references
US · NIOSH

Occupational chemical safety guide

Diphenylamine

Read official guide
JP · NITE

Government GHS classification

H30-C-010-MHLW · FY2018

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 number122-39-4ChEBI ↗
Molecular formulaC12H11NChEBI ↗
Molar mass169.227 g/molChEBI ↗
Monoisotopic mass169.08915 DaChEBI ↗
Formal charge0ChEBI ↗
ChEBI identifierCHEBI:4640ChEBI ↗

Cross-source molecular data

PubChem
Molar mass169.22 g/molPubChem ↗
Exact mass169.089149355 DaPubChem ↗
Computed XLogP3.5PubChem ↗
Topological polar surface area (Ų)12PubChem ↗
H-bond donors1PubChem ↗
H-bond acceptors1PubChem ↗
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
diphenylamine
N-phenylaniline
DMBHHRLKUKUOEG-UHFFFAOYSA-N
c1ccc(Nc2ccccc2)cc1
InChI=1S/C12H11N/c1-3-7-11(8-4-1)13-12-9-5-2-6-10-12/h1-10,13H

Names & synonyms

N-phenylaniline

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

Classification & relationships

ChEBI ontology

Roles recorded in ChEBI

ferroptosis inhibitorantioxidantradical scavengercarotogenesis inhibitorEC 1.3.99.29 [phytoene desaturase (zeta-carotene-forming)] inhibitorantifungal 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 · FY2018 source classification
Diphenylamine · H30-C-010-MHLW
EndpointReported classification
CarcinogenicityCategory 2

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
0.00590922 mol

Uses 169.227 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 · 12 atoms
85.17%
N
Nitrogen · 1 atom
8.28%
H
Hydrogen · 11 atoms
6.55%

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

Sources & record history

Checked 27 Sep 2026
EMBL-EBI ChEBI · CHEBI:4640

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

NCBI PubChem · CID 11487 · 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.