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PETROSELINIC ACID METHYL ESTER is a versatile chemical compound derived from petroselinic acid, a type of fatty acid found in certain plant oils. It is known for its emollient and moisturizing properties, making it a popular ingredient in cosmetic products, as well as in the production of various industrial products such as lubricants and plasticizers. PETROSELINIC ACID METHYL ESTER is also utilized in the manufacture of specialty chemicals and as a solvent in some industrial processes.

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  • 2777-58-4 Structure
  • Basic information

    1. Product Name: PETROSELINIC ACID METHYL ESTER
    2. Synonyms: DELTA 6 TRANS OCTADECENOIC ACID METHYL ESTER;PETROSELAIDIC ACID METHYL ESTER;PETROSELINIC ACID METHYL ESTER;methyl (Z)-octadec-6-enoate;CIS-6-PETROSELINIC METHYL ESTER,1X1ML, H EPTANE 10MG/ML;METHYL PETROSELATE STANDARD FOR GC;6-Octadecenoic acid, methyl ester, (Z)-;cis-6-octadecenoic methyl ester
    3. CAS NO:2777-58-4
    4. Molecular Formula: C19H36O2
    5. Molecular Weight: 296.49
    6. EINECS: 220-470-2
    7. Product Categories: N/A
    8. Mol File: 2777-58-4.mol
  • Chemical Properties

    1. Melting Point: -1°C(lit.)
    2. Boiling Point: 208-210℃ (10 Torr)
    3. Flash Point: -1 °C
    4. Appearance: /Liquid
    5. Density: 0.873g/cm3
    6. Vapor Pressure: 1.07E-05mmHg at 25°C
    7. Refractive Index: 1.4501 (589.3 nm 20℃)
    8. Storage Temp.: −20°C
    9. Solubility: N/A
    10. CAS DataBase Reference: PETROSELINIC ACID METHYL ESTER(CAS DataBase Reference)
    11. NIST Chemistry Reference: PETROSELINIC ACID METHYL ESTER(2777-58-4)
    12. EPA Substance Registry System: PETROSELINIC ACID METHYL ESTER(2777-58-4)
  • Safety Data

    1. Hazard Codes: F,Xn,N
    2. Statements: 11-38-50/53-65-67
    3. Safety Statements: 16-60-61-62-33-29-9-24/25
    4. RIDADR: UN 1206 3/PG 2
    5. WGK Germany: 2
    6. RTECS:
    7. HazardClass: N/A
    8. PackingGroup: N/A
    9. Hazardous Substances Data: 2777-58-4(Hazardous Substances Data)

2777-58-4 Usage

Uses

Used in Cosmetic Industry:
PETROSELINIC ACID METHYL ESTER is used as an emollient and moisturizing agent in skincare and haircare formulations for its ability to provide a smooth and soft texture to the skin and hair, enhancing their overall appearance and feel.
Used in Industrial Production:
PETROSELINIC ACID METHYL ESTER is used as a key ingredient in the production of lubricants and plasticizers, where its emollient properties contribute to the performance and efficiency of these products.
Used in Specialty Chemicals Manufacturing:
PETROSELINIC ACID METHYL ESTER is utilized in the manufacture of specialty chemicals, where its unique properties allow for the creation of innovative and high-quality chemical products.
Used as a Solvent in Industrial Processes:
PETROSELINIC ACID METHYL ESTER serves as a solvent in certain industrial processes, where its ability to dissolve other substances aids in the efficiency and effectiveness of these processes.

Check Digit Verification of cas no

The CAS Registry Mumber 2777-58-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,7 and 7 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2777-58:
(6*2)+(5*7)+(4*7)+(3*7)+(2*5)+(1*8)=114
114 % 10 = 4
So 2777-58-4 is a valid CAS Registry Number.
InChI:InChI=1/C19H36O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19(20)21-2/h13-14H,3-12,15-18H2,1-2H3/b14-13-

2777-58-4 Well-known Company Product Price

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  • Supelco

  • (47198)  cis-6-Octadecenoicacidmethylester  certified reference material, 10 mg/mL in heptane

  • 2777-58-4

  • 000000000000047198

  • 453.96CNY

  • Detail

2777-58-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name PETROSELINIC ACID METHYL ESTER

1.2 Other means of identification

Product number -
Other names PETROSELAIDIC ACID METHYL ESTER

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:2777-58-4 SDS

2777-58-4Relevant articles and documents

Oxygenation of monoenoic fatty acids by CYP175A1, an orphan cytochrome P450 from thermus thermophilus HB27

Goyal, Sandeep,Banerjee, Shibdas,Mazumdar, Shyamalava

, p. 7880 - 7890 (2013/01/15)

The catalytic activity of CYP175A1 toward monooxygenation of saturated and monounsaturated fatty acids of various chain lengths (C16-C24) has been investigated to assess the enzymatic properties of this orphan thermostable cytochrome P450 enzyme. The resu

Polymers and surfactants on the basis of renewable resources

Warwel, Siegfried,Bruese, Falk,Demes, Christoph,Kunz, Michael,Klaas, Mark Ruesch gen

, p. 39 - 48 (2007/10/03)

A new strategy for the preparation of different polymers and special surfactants was developed. First, unsaturated fatty acid methyl esters obtained from plant oils were converted to terminally unsaturated esters and α-olefins by metathesis with ethylene using heterogeneous rhenium or homogeneous ruthenium catalysts. These esters were directly copolymerized with ethylene by an insertion-type palladium-catalyzed polymerization to functionalized polyolefins. Polyesters were synthesized by metathetical dimerization of ω-unsaturated esters and subsequent polycondensation of the produced internally unsaturated dicarboxylic esters or by acidic transesterification with petrochemical diols and additional acyclic diene metathesis polymerization, ω-epoxy fatty acid methyl esters, achieved by a new method of chemo-enzymatic epoxidation, were converted into polyethers with comb-structure catalyzed by aluminoxanes on the one hand and into sugar surfactants by nucleophilic ring-opening with amino carbohydrates on the other hand.

Potentional-controlled catalytic hydrogenation. Effect of palladium catalyst potential on the selectivity of hydrogenation of polyunsaturated fatty acid esters

Froeling, A.,Hornung, F.,Jongh, R. O. de

, p. 123 - 128 (2007/10/02)

Hydrogenation of methyl linoleate on palladium catalysts in solution with tetraalkylammonium perchlorate as electrolyte, leads mainly to the saturated product methyl stearate.At negative potentials of the catalyst electrode controlled at about -1 Volt versus a saturated calomel electrode (SCE) with negligible current passage, the monoenic intermediate is the end product, with the double bond found mainly in the Z configuration at the starting 9- and 12-positions.As expected it was found that methyl oleate was not hydrogenated by the catalyst held at -1.1 Volt, while smooth hydrogenation occurs under identical conditions when the catalyst potential is not controlled.Methyl linoleate leads mainly to dienoic esters at -1.8 V catalyst potential.The effect was applied on a synthetic scale in the hydrogenation of soya bean oil with palladium catalysts, resulting in a considerable increase of selectivity at negative catalyst potentials.

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