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Phorbol 98%: Reliable Diterpene Standard for Pharmacology and Toxicology Research

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Phorbol 98%: Reliable Diterpene Standard for Pharmacology and Toxicology Research

Phorbol 98%: Reliable Diterpene Standard for Pharmacology and Toxicology Research

Phorbol 98% (CAS:17673-25-5) is a high-purity diterpenoid isolated from Croton tiglium seeds, serving as the foundational compound for tumor-promoting phorbol esters like PMA. With ≥98% HPLC-verified purity and characteristic needle crystals, it enables critical research in PKC-mediated carcinogenesis, apoptosis resistance, and multi-drug resistance reversal.

  • Product Name :

    Phorbol
  • CAS No. :

    17673-25-5
  • Appearance :

    White to off-white crystalline powder
  • Specification :

    98%

? Phorbol (Croton Resin) 98%

CAS: 17673-25-5
Molecular Formula: C??H??O?
Molecular Weight: 364.43 g/mol
Appearance: White to off-white crystalline powder


?? Core Value Proposition

High-Purity Tumor Promoter & PKC Pathway Activator
≥98% Purity (HPLC-UV validated, λmax 234 nm)
Mechanistic Research Tool: Serves as the core structure for bioactive esters (e.g., PMA) in PKC-dependent carcinogenesis and immunology studies.
Natural Source Integrity: Sourced from Croton tiglium seeds, preserving native diterpenoid activity.


? Biologically Validated Functions

1. Tumor Promotion Research

  • Acts as a progenitor of tumor-promoting esters (e.g., PMA) in two-stage carcinogenesis models, enabling mechanistic studies of PKC-mediated cell proliferation.

  • Metabolic Activation: Liver microsomes convert phorbol to active esters in vivo, mimicking endogenous tumor promotion pathways.

2. Pharmacological Synergy

  • Enhances cytotoxicity of chemotherapeutics (e.g., doxorubicin) in multidrug-resistant cancer lines via PKCα modulation.


?? Technical Specifications

Parameter Detail
Purity ≥98% (HPLC-DAD, C18 column)
Source Croton tiglium seeds (Xinjiang origin, pesticide-free)
Melting Point 249–251°C (decomposition)
Solubility DMSO (30 mg/mL), ethanol (soluble); water-soluble (1 mg/mL)
Storage -20°C in desiccated amber vials (24-month stability)
Key Impurities Jaceosidin ≤0.2% (HPLC-controlled)
Hazard Classification T+ (Toxic) - R26/27/28

? Research Applications

Oncology & Toxicology

  • Tumor initiation studies: Metabolic precursor for synthesizing PMA (CAS 16561-29-8), used in DMBA-initiated skin carcinogenesis models.

  • Apoptosis resistance research: Modulates PKCε to inhibit anoikis in metastatic cell lines.

Natural Product Chemistry

  • Reference standard for quantifying phorbol esters in Croton extracts via alkaline hydrolysis (HPLC conditions: Diamonsil C18 column, acetonitrile/water gradient).


? Competitive Advantages

1. Sustainable Purification Technology

  • D101 macroporous resin chromatography: Ethanol/water gradient elution achieves 91.08% purity with 62.16% recovery, reducing organic solvent use by 40% vs. silica gel methods.

2. Batch-Specific Bioactivity Data

  • Free alkaline hydrolysis protocol with yield validation reports (included with ≥25 mg orders).

3. Global Compliance Ready

  • Full analytical dossiers support FDA ICH Q3C and EU GMP registration (residual solvent limits: methanol <3000 ppm).


? Packaging & Stability

Quantity Packaging Storage Stability
1 mg Argon-sealed glass vial -20°C 24 months
5 mg Desiccated amber vial -20°C 24 months
25 mg Pharma-grade aluminum can -20°C (dry) 36 months*
100 mg Nitrogen-flushed drum -20°C (dry) 36 months*

*With desiccant; reconstituted solutions stable 3 months at -20°C in DMSO.


?? Safety & Handling

  • Toxicity: LD?? (oral, rat) = 1 mg/kg; use fume hood + nitrile gloves17.

  • Waste Disposal: Inactivate with 10% sodium hypochlorite → neutralize to pH 7 → incinerate.

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