Tris(2,4-di-tert-butylphenyl)phosphate

CAS No. 95906-11-9

Tris(2,4-di-tert-butylphenyl)phosphate( —— )

Catalog No. M25017 CAS No. 95906-11-9

Tris(2,4-di-tert-butylphenyl)phosphate is a natural compound isolated from Vitex negundo L. with anti-inflammatory activity.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
10MG 29 In Stock
25MG 40 In Stock
50MG 57 In Stock
100MG 83 In Stock
200MG Get Quote In Stock
500MG 203 In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Tris(2,4-di-tert-butylphenyl)phosphate
  • Note
    Research use only, not for human use.
  • Brief Description
    Tris(2,4-di-tert-butylphenyl)phosphate is a natural compound isolated from Vitex negundo L. with anti-inflammatory activity.
  • Description
    Tris(2,4-di-tert-butylphenyl)phosphate is a natural compound isolated from Vitex negundo L. with anti-inflammatory activity.
  • In Vitro
    ——
  • In Vivo
    Tris(2,4-di-tert-butylphenyl)phosphate (TDTBPP; 50 mg/kg and 70 mg/kg) exhibits significant anti-inflammatory activity in carrageenan induced paw odema model. Tris(2,4-di-tert-butylphenyl)phosphate (50 mg/kg and 70 mg/kg) reduces the raw paw odema volume significantly.
  • Synonyms
    ——
  • Pathway
    Metabolic Enzyme/Protease
  • Target
    Phospholipase
  • Recptor
    sPLA2
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    95906-11-9
  • Formula Weight
    662.92
  • Molecular Formula
    C42H63O4P
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO:2 mg/mL (3.02 mM; Need ultrasonic);Ethanol:100 mg/mL (150.85 mM; Need ultrasonic)
  • SMILES
    O=P(OC1=C(C(C)(C)C)C=C(C(C)(C)C)C=C1)(OC2=C(C(C)(C)C)C=C(C(C)(C)C)C=C2)OC3=C(C(C)(C)C)C=C(C(C)(C)C)C=C3
  • Chemical Name
    ——

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1.Vinuchakkaravarthy T, et al. Active compound from the leaves of Vitex negundo L. shows anti-inflammatory activity with evidence of inhibition for secretory Phospholipase A(2) through molecular docking. Bioinformation. 2011;7(4):199-206.
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