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Methyl 10-methylundecanoate is an organic compound with the chemical formula C13H26O2. It is a colorless liquid with a fruity, apple-like odor. This ester is formed by the reaction of methyl alcohol (methanol) and 10-methylundecanoic acid, which is a derivative of undecanoic acid with an additional methyl group. Methyl 10-methylundecanoate is commonly used in the fragrance and flavor industry due to its pleasant scent and taste, and it can be found in various applications such as perfumes, cosmetics, and food products. It is also known for its potential use as a biofuel additive and a precursor in the synthesis of other chemicals.

5129-56-6

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5129-56-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5129-56-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,2 and 9 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5129-56:
(6*5)+(5*1)+(4*2)+(3*9)+(2*5)+(1*6)=86
86 % 10 = 6
So 5129-56-6 is a valid CAS Registry Number.
InChI:InChI=1/C13H26O2/c1-12(2)10-8-6-4-5-7-9-11-13(14)15-3/h12H,4-11H2,1-3H3

5129-56-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name METHYL 10-METHYLUNDECANOATE

1.2 Other means of identification

Product number -
Other names Methyl isolaurate

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 -
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More Details:5129-56-6 SDS

5129-56-6Relevant academic research and scientific papers

Isolation of the β-galactosphingolipid coniferoside using a tumor cell proteome reverse affinity protocol

La Clair, James J.,Rodriguez, Abimael D.

experimental part, p. 6645 - 6653 (2011/12/21)

New approaches are vital to the development of marine natural products (MNP) as therapeutic leads. One of the more time consuming aspects of MNP research arises in the connection between structure and function. Here, we describe an isolation protocol that adapts tumor cell proteomes as a vehicle for MNP isolation therein uniting structural and functional analysis. Application of this method to extracts of the sponge Agelas conifera led to the isolation of a unique poly-hydroxybutyrated β-galactosphingolipid, coniferoside.

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