Isopropyl myristate

CAS No. 110-27-0

Isopropyl myristate( Stepan D-50 | FEMA No. 3556 | HSDB 626 | IPM | Isomyst | NSC 406280 )

Catalog No. M23303 CAS No. 110-27-0

Isopropyl myristate is the isopropyl alcohol and myristic acid ester.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
500MG 35 In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Isopropyl myristate
  • Note
    Research use only, not for human use.
  • Brief Description
    Isopropyl myristate is the isopropyl alcohol and myristic acid ester.
  • Description
    Isopropyl myristate is the isopropyl alcohol and myristic acid ester.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    Stepan D-50 | FEMA No. 3556 | HSDB 626 | IPM | Isomyst | NSC 406280
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    Others
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    110-27-0
  • Formula Weight
    270.45
  • Molecular Formula
    C17H34O2
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO:Soluble
  • SMILES
    CCCCCCCCCCCCCC(OC(C)C)=O
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Burgess IF, Silverston P. Head lice. BMJ Clin Evid. 2015 Jan 14;2015. pii: 1703. Review. PubMed PMID: 25587918; PubMed Central PMCID: PMC4294162.
molnova catalog
related products
  • α-Glucosidase-IN-22

    α-Glucosidase-IN-22 is a selective inhibitor of α-glucosidase (IC50=0.64 μM). α-Glucosidase-IN-22 has antidiabetic activity and has potential in type 2 diabetes (T2DM) studies.

  • Arecoline

    Arecoline is an agonist at both muscarinic and nicotinic acetylcholine receptors. It is used in the form of various salts as a ganglionic stimulant, a parasympathomimetic, and a vermifuge, especially in veterinary practice.

  • FTIDC

    FTIDC is a highly potent and selective allosteric antagonist of mGluR1 receptors and shows very weak potency against human and rat mGluR5 receptors.