Transplatin
A diamminedichloroplatinum compound in which the two ammine ligands and two chloro ligands are oriented in a trans planar configuration around the central platinum ion. Unlike its cis-isomer, cisplatin, it does not exhibit any useful pharmacological effect and is toxic. — ChEBI
Safety documents & references
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Identity & molecular properties
Source-linked values| CAS number | 14913-33-8 | ChEBI ↗ |
| Molecular formula | H6Cl2N2Pt | ChEBI ↗ |
| Molar mass | 300.046 g/mol | ChEBI ↗ |
| Monoisotopic mass | 298.95559 Da | ChEBI ↗ |
| Formal charge | 0 | ChEBI ↗ |
| ChEBI identifier | CHEBI:35852 | ChEBI ↗ |
Names & structural identifiers
Copy any identifiertransplatin(SP-4-1)-diamminedichloridoplatinumLXZZYRPGZAFOLE-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-2Names & synonyms
Names are supplied by ChEBI. Trade names and related synonyms may describe a broader product context.
Classification & relationships
ChEBI ontologyRoles recorded in ChEBI
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 massUses 300.046 g/mol from ChEBI. Assumes the substance described by this record; no purity or concentration correction is applied.
Elemental composition
Theoretical mass fractionsPtClNHCalculated 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 associationsSources & record history
Checked 27 Sep 2026Release 255, 9 September 2026. ChEBI three-star (manually annotated) source entry. View original record ↗ · CC BY 4.0
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.