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  • 33057-39-5 Structure
  • Basic information

    1. Product Name: OLEYL STEARATE
    2. Synonyms:
    3. CAS NO:33057-39-5
    4. Molecular Formula:
    5. Molecular Weight: 0
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 33057-39-5.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: OLEYL STEARATE(CAS DataBase Reference)
    10. NIST Chemistry Reference: OLEYL STEARATE(33057-39-5)
    11. EPA Substance Registry System: OLEYL STEARATE(33057-39-5)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 33057-39-5(Hazardous Substances Data)

33057-39-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 33057-39-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,0,5 and 7 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 33057-39:
(7*3)+(6*3)+(5*0)+(4*5)+(3*7)+(2*3)+(1*9)=95
95 % 10 = 5
So 33057-39-5 is a valid CAS Registry Number.

33057-39-5Downstream Products

33057-39-5Relevant articles and documents

Enzymatic esterification of fatty acid esters by tetraethylammonium amino acid ionic liquids-coated Candida rugosa lipase

Abdul Rahman, Mohd Basyaruddin,Jumbri, Khairulazhar,Mohd Ali Hanafiah, Nurul Ain,Abdulmalek, Emilia,Tejo, Bimo Ario,Basri, Mahiran,Salleh, Abu Bakar

experimental part, p. 61 - 65 (2012/07/13)

Enzymatic production of fatty acid esters from the esterification of oleyl alcohol with various fatty acids was investigated by using two new tetraethylammonium amino acid ionic liquids-coated Candida rugosa lipase (ILs-CRL) as biocatalysts in hexane. Both enzyme derivatives were prepared by mixing Candida rugosa lipase with tetraethylammonium l-histidinate (IL1) and tetraethylammonium l-asparaginate (IL2). The ILs-CRL system containing the equivalent protein concentration as in CRL showed higher esterification activity especially on medium chain fatty acids (C12-C16) as compared to non-coated CRL. Hydrophilicity of ILs may play an important role in hydrogen bonding with enzyme surface and consequently stabilize the ILs-CRL.

Engkabang fat esters for cosmeceutical formulation

Gani, Siti Salwa Abd,Basri, Mahiran,Rahman, Mohd Basyaruddin Abdul,Kassim, Anuar,Rahman, Raja Noor Zaliha Raja Abd,Salleh, Abu Bakar,Ismail, Zahariah

experimental part, p. 227 - 233 (2012/05/05)

Engkabang fat esters were synthesized from engkabang fat using an enzyme as catalyst. The main composition of the fat esters were oleyl palmitate, oleyl stearate and oleyl oleate. The percentage yield was 93.67%. Ternary phase diagrams systems containing fat esters/surfactant/water were constructed. Several regions appeared in the ternary phase diagrams such as isotropic, homogenous, liquid crystal, two-phase and three-phase regions. Increasing the hydrophilic-lipophilic balance value of the used surfactants gave a larger homogenous and isotropic region in ternary phase diagrams of engkabang fat esters/nonionic surfactant/deionized water. Isotropic and homogenous regions in the ternary phase diagram of engkabang fat esters: PEG-40 hydrogenated castor oil (2:1)/polyoxyethylene(20) sorbitan tri-oleate/deionized water, was the largest when compared to the other ternary phase diagrams. The isotropic and homogenous region can be used as a medium in formulation of cosmetics and pharmaceutical products such as creams, lotions, balms and lipsticks. AOCS 2010.

Synthesis of Fatty Acid Ester by Corynebacterium sp. S-401

Seo, Chull Won,Yamada, Yasuhiro,Okada, Hirosuke

, p. 405 - 410 (2007/10/02)

Resting cells and acetone-dried cells of Corynebacterium sp.S-401 catalyzed the fatty acid ester synthesis of various alcohols and fatty acids.These reactions were carried out in phosphate buffer and/or organic solvents.In some cases synthetic reactions of esters in nonpolar solvents, such as n-hexane and benzene, gave better results compared with those obtained in phosphate buffer.

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