1730-89-8

Basic information

• Product Name: (S)-(+)-4-METHYLHEXANOIC ACID
• Synonyms: (S)-(+)-4-METHYLHEXANOIC ACID
• CAS NO: 1730-89-8
• Molecular Formula: C₇H₁₄O₂
• Molecular Weight: 130.179992675781
• Mol File: 1730-89-8.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 215.253 °C at 760 mmHg
• Flash Point: 102.782 °C
• Appearance: /
• Density: 0.936 g/cm³
• Vapor Pressure: 0.058mmHg at 25°C
• Refractive Index: 1.431
• CAS DataBase Reference: (S)-(+)-4-METHYLHEXANOIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-(+)-4-METHYLHEXANOIC ACID(1730-89-8)
• EPA Substance Registry System: (S)-(+)-4-METHYLHEXANOIC ACID(1730-89-8)

Safety Data

• Hazardous Substances Data: 1730-89-8(Hazardous Substances Data)

Usage

Description

(S)-(+)-4-METHYLHEXANOIC ACID, with the molecular formula C7H14O2, is a chiral compound that possesses a non-superimposable mirror image. The (S)-(+)-enantiomer is the specific form being described here. This colorless liquid exhibits a pungent odor and is widely recognized for its applications across various industries.

Uses

Used in Pharmaceutical Industry:
(S)-(+)-4-METHYLHEXANOIC ACID is used as an active pharmaceutical ingredient for its potential therapeutic properties, contributing to the development of new medications.
Used in Fragrance Industry:
(S)-(+)-4-METHYLHEXANOIC ACID is used as a scent component for its distinctive aroma, enhancing the olfactory profiles of various fragrances.
Used in Flavoring Industry:
(S)-(+)-4-METHYLHEXANOIC ACID is used as a flavor enhancer for its ability to impart unique taste characteristics to food and beverages.
Used in Polymer Production:
(S)-(+)-4-METHYLHEXANOIC ACID is used as a monomer or a building block in the synthesis of polymers, contributing to the creation of materials with specific properties for various applications.
Used in Organic Synthesis:
(S)-(+)-4-METHYLHEXANOIC ACID is used as a precursor in organic synthesis, enabling the production of a range of chemical compounds for industrial and commercial use.
Overall, (S)-(+)-4-METHYLHEXANOIC ACID is a versatile chemical compound that plays a significant role in the development and manufacturing processes across different sectors, making it an indispensable asset in the chemical industry.

InChI:InChI=1/C7H14O2/c1-3-6(2)4-5-7(8)9/h6H,3-5H2,1-2H3,(H,8,9)/t6-/m0/s1

Upstream product

• 53353-03-0 (R)-(-)-2,6-dimethyl-2-octene 

Downstream Products

• 3350-10-5 N-[(R)-4-benzyloxycarbonylamino-2-((S)-6-methyl-octanoylamino)-butyryl]-L_s-threonine methyl ester 
• 120581-48-8 N-[(R)-4-benzyloxycarbonylamino-2-((S)-6-methyl-octanoylamino)-butyryl]-L_s-threonine 
• 504-99-4 (6S)-6-methyloctanoic acid 
• 5746-59-8 (S)-(+)-14-methylhexadecanoic acid 
• 78976-07-5 trans-(S,S)-(-)-2,2'-Bis(4-methylhexyl)azobenzol 
• 78976-06-4 cis-(S,S)-(-)-2,2'-Bis(4-methylhexyl)azobenzol 
• 78976-09-7 trans-(S,S)-(+)-4,4'-Bis(4-methylhexyl)azobenzol 
• 78976-08-6 cis-(S,S)-(+)-4,4'-Bis(4-methylhexyl)azobenzol 
• 78976-18-8 (S)-(+)-1-(4-Methylhexyl)-2-nitrobenzol 
• 78976-20-2 (S)-(+)-1-(4-Methylhexyl)-4-nitrobenzol 
• 6839-54-9 (S)-(+)-4-Methyl-1-phenyl-1-hexanon 

Relevant articles and documents

Synthese von optisch aktiven Trogoderma-Pheromonen durch Kolbe-Elektrolyse

The (R)-(-)-enantiomers of (Z)- (1) and (E)-14-methyl-8-hexadecen-1-ol (2) have been synthesized by coelectrolysis of (R)-(-)-4-methylhexanoic acid (7) with 12-(tetrahydro-2-pyranyloxy)-4-dodecynoic acid (8) and its subsequent hydrogenation.The acid 7 was prepared in high optical purity from (S)-(-)-citronellol (3) by conversion of the hydroxyl group to a methyl substituent and subsequent cleavage of (R)-(-)-2,6-dimethyl-2-octene (4) with ozone.By alkylation of 4-pentynoic acid (5) with 1-bromo-7-(tetrahydro-2-pyranyloxy)heptane (6) the alkynoic acid 8 was synthesized.