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METHYL 12-OXOOCTADECANOATE, also known as a long chain keto fatty acid, is a light brown solid that has been studied for its reaction with hydrazoic acid. It is characterized by its unique chemical properties and potential applications in various industries.

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  • 2380-27-0 Structure
  • Basic information

    1. Product Name: METHYL 12-OXOOCTADECANOATE
    2. Synonyms: 12-ketostearic acid methyl ester;Methyl 12-oxooctadecanoate 98%;METHYL 12-OXOOCTADECANOATE;12-OXOOCTADECANOIC ACID METHYL ESTER;12-Oxostearic acid, methyl ester;Methyl 12-ketostearate;Methyl 12-oxostearate
    3. CAS NO:2380-27-0
    4. Molecular Formula: C19H36O3
    5. Molecular Weight: 312.49
    6. EINECS: N/A
    7. Product Categories: Fatty Acid Derivatives & Lipids;Glycerols;C12 to C63;Carbonyl Compounds;Esters;Mixed Fatty Acids
    8. Mol File: 2380-27-0.mol
  • Chemical Properties

    1. Melting Point: 46-48 °C(lit.)
    2. Boiling Point: 178-180 °C/0.8 mmHg(lit.)
    3. Flash Point: 113 °C
    4. Appearance: /
    5. Density: 1.0345 (rough estimate)
    6. Vapor Pressure: 1.96E-06mmHg at 25°C
    7. Refractive Index: 1.4200 (estimate)
    8. Storage Temp.: -20°C Freezer
    9. Solubility: Chloroform (Slightly), Methanol (Slightly)
    10. CAS DataBase Reference: METHYL 12-OXOOCTADECANOATE(CAS DataBase Reference)
    11. NIST Chemistry Reference: METHYL 12-OXOOCTADECANOATE(2380-27-0)
    12. EPA Substance Registry System: METHYL 12-OXOOCTADECANOATE(2380-27-0)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany: 3
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 2380-27-0(Hazardous Substances Data)

2380-27-0 Usage

Uses

1. Used in Pharmaceutical Industry:
METHYL 12-OXOOCTADECANOATE is used as a chemical intermediate for the preparation of various pharmaceutical compounds. Its application is due to its ability to react with other chemicals, such as thiocarbohydrazide, to form derivatives with potential therapeutic properties.
2. Used in Chemical Synthesis:
METHYL 12-OXOOCTADECANOATE serves as a key component in the synthesis of complex organic molecules. Its application is attributed to its reactivity and the formation of valuable products, such as methyl hexahydro-3-hexyl-6-thioxo-1,2,4,5-tetrazine-3-undecanoate, which is a hexahydrothioxotetrazine fatty derivative.

Check Digit Verification of cas no

The CAS Registry Mumber 2380-27-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,8 and 0 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2380-27:
(6*2)+(5*3)+(4*8)+(3*0)+(2*2)+(1*7)=70
70 % 10 = 0
So 2380-27-0 is a valid CAS Registry Number.
InChI:InChI=1/C19H36O3/c1-3-4-5-12-15-18(20)16-13-10-8-6-7-9-11-14-17-19(21)22-2/h3-17H2,1-2H3

2380-27-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name METHYL 12-OXOOCTADECANOATE

1.2 Other means of identification

Product number -
Other names Methyl 12-ketostearate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:2380-27-0 SDS

2380-27-0Relevant articles and documents

Synthesis, Characterisation, and Transformations of a Lipid Cyclic Peroxide

Bascetta, Emanuele,Gunstone, Frank D.,Scrimgeour, Charles M. S.

, p. 2199 - 2206 (2007/10/02)

Photosensitised oxidation of (9E,11E)-methyl octadeca-9,11-dienoate gave an unsaturated cyclic peroxide (epidioxide) in high yield.This was characterised spectroscopically.The peroxide underwent facile rearrangement to a furanoid ester under a variety of reaction conditions.Catalytic reduction of the unsaturated peroxide cleaved the O-O bond.Bromination and epoxidation gave dibromo and epoxy esters respectively with the peroxide group still intact.

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