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CAS

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5129-53-3

Methyl 7-methyloctanoate, also known as methyl nonyl ketone, is an organic compound with the chemical formula C10H20O. It is a colorless liquid with a fruity, apple-like odor and is derived from the esterification of 7-methyloctanoic acid and methanol. This chemical is commonly used in the fragrance industry as a scent component in various products, such as perfumes, soaps, and cosmetics. Additionally, it can be found in some natural essential oils, like those from the orange tree. Methyl 7-methyloctanoate is also used as a flavoring agent in food and beverages, contributing to the characteristic taste of certain fruits and confectionery items.

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  • 5129-53-3 Structure

  • Basic information

    1. Product Name: METHYL 7-METHYLOCTANOATE
    2. Synonyms: METHYL 7-METHYLOCTANOATE
    3. CAS NO:5129-53-3
    4. Molecular Formula: C10H20O2
    5. Molecular Weight: 172.26
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 5129-53-3.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: METHYL 7-METHYLOCTANOATE(CAS DataBase Reference)
    10. NIST Chemistry Reference: METHYL 7-METHYLOCTANOATE(5129-53-3)
    11. EPA Substance Registry System: METHYL 7-METHYLOCTANOATE(5129-53-3)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 5129-53-3(Hazardous Substances Data)

5129-53-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5129-53-3 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 3 respectively.
Calculate Digit Verification of CAS Registry Number 5129-53:
(6*5)+(5*1)+(4*2)+(3*9)+(2*5)+(1*3)=83
83 % 10 = 3
So 5129-53-3 is a valid CAS Registry Number.

5129-53-3SDS

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 7-METHYLOCTANOATE

1.2 Other means of identification

Product number -
Other names 7-methyloctanoic 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:5129-53-3 SDS

5129-53-3Relevant articles and documents

PROCESS FOR PREPARING AN ALCOHOL FROM HYDROCARBONS

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Paragraph 0056-0065; 0073-0074, (2020/12/25)

The invention provides a process for preparing an alcohol by hydrogenating an ester which is obtained by alkoxycarbonylating a C2 to C20 hydrocarbon having at least one multiple bond, preferably having at least one olefinic double bond, in which the homogeneous catalyst system used is separated from the product mixture by means of membrane separation. In a development of the present invention, the ester thus formed is converted to another ester by transesterification and then hydrogenated.

Isolation of new aliphatic sulfates and sulfamate as the Daphnia kairomones inducing morphological change of a phytoplankton Scenedesmus gutwinskii

Yasumoto, Ko,Nishigami, Akinori,Aoi, Hiroaki,Tsuchihashi, Chise,Kasai, Fumie,Kusumi, Takenori,Ooi, Takashi

, p. 133 - 136 (2008/09/20)

New aliphatic sulfates and sulfamates were isolated from Daphnia pulex as the Daphnia kairomones that induced morphological defense of a freshwater phytoplankton Scenedesmus gutwinskii var. heterospina (NIES-802). Their structures were determined by spectroscopic and synthetic studies.

Group of anti-cancer compounds with specific structure and their production method

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Page/Page column 26, (2010/11/23)

Compounds containing a specific branched chain end terminal group, which is isopropyl, sec.-butyl, or tert.-butyl; a polar leading group; and long-chain aliphatic, non-cyclic, saturated or unsaturated, hydrocarbon group linking them; and having anti-cancer and immune boosting activity.

Topically applied circulation enhancing agent and skin and hair cosmetic and bath agent containing the same

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Page/Page column 8, (2008/06/13)

A topically applied circulation enhancing agent suited for application over the entire body which has good transdermal absorptivity and causes little irritation is provided. A topically applied circulation enhancing agent is provided which contains a fatty acid ester denoted by general formula (1):

Oils with heterogenous chain lengths

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Page/Page column 7, (2008/06/13)

Oils containing a triacylglycerol polyol ester and a non-glycerol polyol ester are described, as well as methods of making such oils. Methods for improving lubrication properties of a vegetable oil also are described.

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