Dirhodium(II) Octanoate

GTC-343

Rhodium Compounds

Dirhodium(II) Octanoate

CAS No.
73482-96-9
Catalogue ID
GTC-343

Dirhodium(II) Octanoate, CAS 73482-96-9. Source-derived identification, physical data and applications are provided for catalogue reference; request the current specification, COA and SDS for the required grade.

Catalogue aliases / related identifiers

Rhodium(II) octanoate dimer; Tetrakis(octanoato)dirhodium(II); Dirhodium tetraoctanoate; Rhodium octanoate dimer; Tetrakis(octanoate)dirhodium; Rhodium(2+) octanoate dimer; Rhodium(II) octanoate; Dirhodium(II) tetrakisoctanoate

Supplied catalogue source: GTC-343 · Page 72

Reference data — confirm before ordering or use

The information below is a structured migration from the supplied catalogue snapshot. It is not a current product specification, COA or SDS. Confirm the actual supplier, grade, batch documents, classification, packing and destination requirements for your enquiry.


Basic Information of Dirhodium(II) Octanoate

CAS No.73482-96-9
EC No.277-477-2
Chemical FormulaRh₂(O₂CC₇H₁₅)₄
Molecular Weightapprox. 1076 g/mol
AppearanceDark green to bluish-green powder or waxy solid
OdorSlight carboxylic
Melting pointapprox. 40–60 °C (softens)
Boiling pointDecomposes before boiling
Densityapprox. 1.1–1.3 g/cm³
SolubilityHighly soluble in hydrocarbons, toluene, hexane, dichloromethane; insoluble in water
Nature (hazards)May cause skin and eye irritation, harmful if swallowed or inhaled, toxic to aquatic life with long lasting effects
RIDADRUN 3077, Environmentally hazardous substance, solid/liquid, n.o.s. (Dirhodium(II) octanoate), Class 9, Packing Group III
Chemical StructureMolecular Structure of Dirhodium(II) Octanoate

Primary Applications of Dirhodium(II) Octanoate

Dirhodium(II) Octanoate is the gold-standard Rh(II) catalyst for carbene and nitrene transfer reactions, delivering exceptional selectivity in complex molecule synthesis.

  1. C–H Insertion & Functionalization
    Catalyzes highly selective intramolecular and intermolecular C–H insertion of diazo compounds, enabling efficient construction of C–C bonds in natural products and pharmaceutical intermediates.

  2. Cyclopropanation of Alkenes
    Provides excellent diastereocontrol and enantioselectivity in cyclopropanation of olefins with diazoesters, delivering cyclopropane building blocks for drug discovery and agrochemicals.

  3. Nitrene Transfer & Aziridination
    Enables stereoselective aziridination of alkenes and amidation of C–H bonds using nitrene sources, offering powerful strategies for nitrogen-containing heterocycles.

  4. O–H & N–H Insertion
    Facilitates insertion into alcohols and amines to form ethers and amines, providing mild, selective routes to oxygenated and nitrogenated compounds.

  5. Pharmaceutical & Natural Product Synthesis
    Widely applied in late-stage functionalization and key bond-forming steps of complex APIs and natural products, leveraging its high reactivity and functional group tolerance.

  6. Catalyst Development & Asymmetric Catalysis
    Serves as a standard Rh(II) source for chiral ligand screening and development of enantioselective dirhodium catalysts in academic and industrial R&D.


  • Superior Purity & Solubility
    Advanced quality controls ensure high Rh content, minimal impurities, and excellent solubility in non-polar solvents for maximum catalytic activity.

  • Secure Precious Metal Sourcing
    Transparent, responsible rhodium procurement with inventory buffering to provide supply stability and competitive pricing.

  • Technical Catalysis Support
    Dedicated specialists offer guidance on diazo/nitrene precursor selection, reaction optimization, enantioselectivity tuning, and scale-up for maximum efficiency.

  • Comprehensive Regulatory Compliance
    Full COA, REACH, RoHS, and detailed SDS documentation to facilitate seamless integration into pharmaceutical and fine chemical operations.

  • Sustainability & Recycling Programs
    Ethical sourcing practices and rhodium recovery/recycling programs aligned with ESG objectives and sustainable chemistry principles.


Hazards Classification

  • GHS Classification: Skin Irritation (Category 2); Eye Irritation (Category 2A); Specific Target Organ Toxicity, Single Exposure (respiratory) (Category 3); Aquatic Chronic (Category 3)

  • Hazard Statements: H315: Causes skin irritation; H319: Causes serious eye irritation; H335: May cause respiratory irritation; H413: May cause long lasting harmful effects to aquatic life

  • UN Number: UN 3077

  • Hazard Class: 9 (Miscellaneous dangerous substances and articles)

  • Packing Group: III

GHS07
GHS07: Exclamation mark (irritant, respiratory)
GHS09
GHS09: Environment (aquatic hazard)
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  • 01Current specification
  • 02Batch or sample COA
  • 03Product- and supplier-specific SDS
  • 04Packing and shipping review
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