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8-Octadecenoic acid methyl ester, also known as methyl oleate, is a chemical compound derived from the esterification of oleic acid with methanol. It is a colorless to pale yellow liquid with a slight characteristic odor. This unsaturated fatty acid ester has the molecular formula C19H36O2 and a molecular weight of 296.49 g/mol. Methyl oleate is widely used in various industries, including the production of biodiesel, as a lubricant, and in the manufacturing of cosmetics and pharmaceuticals. It is also a key component in the synthesis of various chemicals and polymers. The compound is derived from renewable sources, such as vegetable oils, making it an environmentally friendly alternative to petrochemical-based products.

2345-29-1

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2345-29-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2345-29-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,4 and 5 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2345-29:
(6*2)+(5*3)+(4*4)+(3*5)+(2*2)+(1*9)=71
71 % 10 = 1
So 2345-29-1 is a valid CAS Registry Number.

2345-29-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 8-octadecenoic acid methyl ester

1.2 Other means of identification

Product number -
Other names Δ8-Octadecensaeure-methylester

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:2345-29-1 SDS

2345-29-1Downstream Products

2345-29-1Relevant academic research and scientific papers

Mild method for the selective esterification of carboxylic acids based on the Garegg-samuelsson reaction

Morcillo, Sara P.,Alvarez De Cienfuegos, Luis,Mota, Antonio J.,Justicia, Jose,Robles, Rafael

experimental part, p. 2277 - 2281 (2011/05/19)

A mild method for the selective esterification of primary alcohols is described. The use of different phosphines, I2, and imidazole allows the selective esterification of a wide variety of acids with excellent results. The generation of a bulky phosphonium-carboxylate salt as intermediate could justify the selectivity observed in this process. Additionally, amides also can be synthesized with use of this method.

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