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Chemical substance record

Cisplatin

15663-27-1H6Cl2N2Pt300.046 g/mol
Coordination CompoundChEBI source record

A diamminedichloroplatinum compound in which the two ammine ligands and two chloro ligands are oriented in a cis planar configuration around the central platinum ion. An anticancer drug that interacts with, and forms cross-links between, DNA and proteins, it is used as a neoplasm inhibitor to treat solid tumours, primarily of the testis and ovary. Commonly but incorrectly described as an alkylating agent due to its mechanism of action (but it lacks alkyl groups). — ChEBI

Safety references

Safety documents & references

1 indexed references
JP · NITE

Government GHS classification

H30-C-023-MHLW · FY2018

View classification

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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 number15663-27-1ChEBI ↗
Molecular formulaH6Cl2N2PtChEBI ↗
Molar mass300.046 g/molChEBI ↗
Monoisotopic mass298.95559 DaChEBI ↗
Formal charge0ChEBI ↗
ChEBI identifierCHEBI:27899ChEBI ↗

Cross-source molecular data

PubChem
Molar mass300.05 g/molPubChem ↗
Exact mass298.955598 DaPubChem ↗

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
cisplatin
(SP-4-2)-diamminedichloridoplatinum
LXZZYRPGZAFOLE-UHFFFAOYSA-L
[H][N]([H])([H])[Pt]([Cl])([Cl])[N]([H])([H])[H]
InChI=1S/2ClH.2H3N.Pt/h2*1H;2*1H3;/q;;;;+2/p-2

Names & synonyms

(SP-4-2)-diamminedichloridoplatinum(SP-4-2)-diamminedichloroplatinumBriplatincis-diamminedichloridoplatinum(II)cis-diamminedichloroplatinum(II)CismaplatcisplatinecisplatinocisplatinumLederplatinNeoplatinPlatinex

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 inducerrenoprotective agentantifibrotic agentmutagenantineoplastic agentantimalarialphotosensitizing agentcross-linking reagentgenotoxinnephrotoxic agent

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
(SP-4-2)-Diamminedichloroplatinum (Cisplatin) · H30-C-023-MHLW
EndpointReported classification
CarcinogenicityCategory 1B

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
0.00333282 mol

Uses 300.046 g/mol from ChEBI. Assumes the substance described by this record; no purity or concentration correction is applied.

Elemental composition

Theoretical mass fractions
Pt
Platinum · 1 atom
65.02%
Cl
Chlorine · 2 atoms
23.63%
N
Nitrogen · 2 atoms
9.34%
H
Hydrogen · 6 atoms
2.02%

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
Use of cultured cells of kidney origin to assess specific cytotoxic effects of nephrotoxins. ↗Toxicology in vitro : an international journal published in association with BIBRA · 2003 Feb · PMID 12537968
DE2318020 · Patent reference ↗Patent cross-reference supplied by ChEBI. Association alone does not establish claim scope.
DE2329485 · 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:27899

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

NCBI PubChem · CID 84691 · 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.