4-methyloctanoic acid

Available forms:COA

pd_proNo:474400-2222db6a-f9c3-45f2-9411-f9e69e1076cb

pd_productuse:

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Detailed introduction

Reputable manufacturer supply 4-methyloctanoic acid 54947-74-9 in stock with high standard

  • Molecular Formula:C9H18O2
  • Molecular Weight:158.241
  • Appearance/Colour:COA 
  • Vapor Pressure:0.0057mmHg at 25°C 
  • Melting Point:-29.5°C (estimate) 
  • Refractive Index:n20/D 1.433(lit.)  
  • Boiling Point:253.4 °C at 760 mmHg 
  • PKA:4.78±0.10(Predicted) 
  • Flash Point:129.7 °C 
  • PSA:37.30000 
  • Density:0.919 g/cm3 
  • LogP:2.67750 

4-Methyloctanoic acid(Cas 54947-74-9) Usage

Biochem/physiol Actions

Taste at 10 ppm

Physical properties

4-Methyloctanoic acid is one of the acids mainly responsible for the so-called "soo" odour of mutton. The analogue 4-Ethyloctanoic acid (found in Virginia tobacco and Costus root oil) also has a related goaty odor; this analog has the lowest threshold of all the fatty acids at 1.8 ppb. 4-Methyloctanoic acid is used in flavours for cheese, meat, tobacco and (possibly) fish. Normal use levels in finished consumer product: up to 3 ppm.

Aroma threshold values

Aroma characteristics at 1.0% in PG: waxy, fatty, meaty, reheated beef-like with a slightly lactonic cheesy nuance

Taste threshold values

Taste characteristics at 10 ppm: fatty, waxy, creamy and lactonic with a satiating fatty mouthfeel and metallic nuances.

General Description

4-Methyloctanoic acid is a branched fatty acid commonly used in the flavor and fragrance industries. 4-Methyloctanoic acid gives sweaty and goaty flavors to the mutton meat and goat′s milk cheese, respectively.

InChI:InChI=1/C9H18O2/c1-3-4-5-8(2)6-7-9(10)11/h8H,3-7H2,1-2H3,(H,10,11)/p-1/t8-/m0/s1

54947-74-9 Relevant articles

One-Step Synthesis of Racemic 4-Methyloctanoic Acid, a Component of the Aggregation Pheromone of Oryctes rhinoceros

Sultanov,Ismagilov,Dzhemilev

, p. 1122 - 1123 (2013)

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Pheromone synthesis. Part 258. Synthesis of the enantiomers of the beetle pheromones ethyl 4-methylheptanoate, 4-methyloctanoic acid and 4-methyl-1-nonanol, and HPLC analysis of their derivatives to determine their enantiomeric purities

Mori, Kenji,Akasaka, Kazuaki

, p. 182 - 187 (2018/10/16)

The enantiomers of citronellal have been...

New synthesis of vanillin by degradation of lignin in presence of functional basic ionic liquid

Yi, Fengping,Jiang, Xiaoyan,Niu, Jihua,Zhang, Lirong,Wang, Zhen

, p. 885 - 888 (2015/02/05)

The degradation of lignin catalyzed by f...

Method for Producing Isononanoic Acid Esters, Starting from 2-Ethyl Hexanol

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Paragraph 0081-0087, (2015/06/17)

A Process for preparing carboxylic ester...

Method for Producing Isononanoic Acids from 2-Ethyl Hexanol

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Paragraph 0062-0071, (2015/07/15)

Process for preparing isononanoic acid p...

54947-74-9 Process route

lignin
9005-53-2

lignin

N-butylformamide
871-71-6

N-butylformamide

rac-4-methyloctanoic acid
54947-74-9

rac-4-methyloctanoic acid

2-methoxy-4-n-propylphenol
2785-87-7

2-methoxy-4-n-propylphenol

3-methoxy-4-hydroxybenzoic acid
121-34-6

3-methoxy-4-hydroxybenzoic acid

Homovanillic acid
306-08-1

Homovanillic acid

vanillin
121-33-5,8014-42-4

vanillin

2-methoxy-phenol
90-05-1

2-methoxy-phenol

syringic aldehyde
134-96-3

syringic aldehyde

Conditions
Conditions Yield
With iron(III) chloride; In water; at 130 ℃; for 2h; Ionic liquid;
2-Ethylhexyl alcohol
104-76-7

2-Ethylhexyl alcohol

carbon monoxide
201230-82-2

carbon monoxide

2,5-dimethylheptanoic acid
15313-67-4

2,5-dimethylheptanoic acid

methyl ethyl caproic acid
504-99-4

methyl ethyl caproic acid

3-ethylheptanoic acid
14272-47-0,42330-40-5,57403-75-5

3-ethylheptanoic acid

2-ethylheptanoic acid
3274-29-1

2-ethylheptanoic acid

acide 2,3-dimethylheptanoique
67061-25-0

acide 2,3-dimethylheptanoique

rac-4-methyloctanoic acid
54947-74-9

rac-4-methyloctanoic acid

2-ethyl-4-methylhexanoic acid
1192592-61-2

2-ethyl-4-methylhexanoic acid

Conditions
Conditions Yield
2-Ethylhexyl alcohol; at 350 ℃; for 1h; Inert atmosphere; Gas phase;
carbon monoxide; With hydrogen; at 140 ℃; for 2h; under 142514 Torr;
With oxygen; potassium hydroxide; In water; at 50 ℃; for 6h; under 760.051 Torr;
9.3 %Chromat.
25.7 %Chromat.
8.4 %Chromat.
20.9 %Chromat.
12.3 %Chromat.
2-Ethylhexyl alcohol; at 350 ℃; Inert atmosphere;
carbon monoxide; With hydrogen; rhodium (III) 2-ethylhexanoate; at 140 ℃; for 2h; under 142514 Torr; pH=10;
With oxygen; potassium hydroxide; at 50 ℃; for 6h;

54947-74-9 Upstream products

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54947-74-9 Downstream products

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    (R)-4-methyloctanoic acid ethyl ester

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    (3S,5R)-5-Methyl-3-((4R,5S)-4-methyl-2-oxo-5-phenyl-oxazolidine-3-carbonyl)-nonanoic Acid Tert-butyl Ester

  • 56196-53-3
    56196-53-3

    (+/-)-Ethyl 4-methyloctanoate

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