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Methyl-6-methylheptanoate, also known as 6-methyl-2-heptanone, is an organic compound with the chemical formula C9H18O. It is a colorless liquid with a fruity, apple-like odor and is commonly used as a flavoring agent in the food and beverage industry. This ester is formed by the reaction of 6-methyl-2-heptanol and methyl acetate, and it is characterized by its molecular weight of 142.24 g/mol and a density of approximately 0.84 g/cm3. Methyl-6-methylheptanoate is insoluble in water but soluble in most organic solvents, making it a versatile compound for various applications.

2519-37-1

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2519-37-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2519-37-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,1 and 9 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2519-37:
(6*2)+(5*5)+(4*1)+(3*9)+(2*3)+(1*7)=81
81 % 10 = 1
So 2519-37-1 is a valid CAS Registry Number.

2519-37-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-methyloctanoate

1.2 Other means of identification

Product number -
Other names 6-Methyl-heptansaeure-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:2519-37-1 SDS

2519-37-1Relevant 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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