68778-93-8

Basic information

• Product Name: (2E,6E,10E,14E,18E)-3,7,11,15,19,23-hexamethyltetracosa-2,6,10,14,18,22-hexaen-1-ol
• Synonyms: (2E,6E,10E,14E,18E)-3,7,11,15,19,23-hexamethyltetracosa-2,6,10,14,18,22-hexaen-1-ol
• CAS NO: 68778-93-8
• Molecular Weight: 426.726
• Mol File: 68778-93-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (2E,6E,10E,14E,18E)-3,7,11,15,19,23-hexamethyltetracosa-2,6,10,14,18,22-hexaen-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (2E,6E,10E,14E,18E)-3,7,11,15,19,23-hexamethyltetracosa-2,6,10,14,18,22-hexaen-1-ol(68778-93-8)
• EPA Substance Registry System: (2E,6E,10E,14E,18E)-3,7,11,15,19,23-hexamethyltetracosa-2,6,10,14,18,22-hexaen-1-ol(68778-93-8)

Safety Data

• Hazardous Substances Data: 68778-93-8(Hazardous Substances Data)

Usage

Description

(2E,6E,10E,14E,18E)-3,7,11,15,19,23-hexamethyltetracosa-2,6,10,14,18,22-hexaen-1-ol is a long-chain polyunsaturated alcohol with 24 carbon atoms and multiple double bonds. It is classified as a long-chain alcohol due to the presence of the hydroxyl functional group. This chemical compound has a hydrophobic nature and potential uses in various industries.

Uses

Used in Cosmetics Industry:
(2E,6E,10E,14E,18E)-3,7,11,15,19,23-hexamethyltetracosa-2,6,10,14,18,22-hexaen-1-ol is used as an ingredient in cosmetics for its hydrophobic properties, which can help improve the texture and stability of cosmetic products.
Used in Pharmaceutical Industry:
(2E,6E,10E,14E,18E)-3,7,11,15,19,23-hexamethyltetracosa-2,6,10,14,18,22-hexaen-1-ol is used as a precursor in the synthesis of pharmaceutical compounds, owing to its unique chemical structure and long-chain alcohol properties.
Used in Organic Synthesis:
(2E,6E,10E,14E,18E)-3,7,11,15,19,23-hexamethyltetracosa-2,6,10,14,18,22-hexaen-1-ol is used as a starting material in organic synthesis for the production of various chemical compounds, taking advantage of its long-chain and polyunsaturated nature.

Upstream product

• 68690-47-1 1-methyl-4-{[(2E,6E,10E)-3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraen-1-yl]sulfonyl}benzene 
• 68690-51-7 all-trans-1-benzyloxy-3,7,11,15-tetramethyl-9-p-tolylsulfonyl-2,6,10,14-hexadecatetraene 
• 24034-73-9 Geranylgeraniol 
• 50848-64-1 2E,6E,10E-geranylgeranyl bromide 
• 68690-53-9 all-trans-1-benzyloxy-3,7,11,15,19,23-hexamethyl-9-(p-tolylsulfonyl)-2,6,10,14,18,22-tetracosahexaene 
• 358-71-4 isopentyl pyrophosphate 
• 6699-20-3 (E,E,E)-geranylgeranyl diphosphate 
• 372-97-4 farnesyl pyrophosphate 
• 358-72-5 dimethylallyl diphosphate 

Downstream Products

• 1597486-91-3 C₅₆H₇₈O₄S 
• 2124-57-4 menaquinone-7 
• 68731-63-5 1-methyl-4-{[(2E,6E,10E,14E,18E,22E,26E)-3,7,11,15,19,23,27,31-octamethyldotriaconta-2,6,10,14,18,22,26,30-octaen-1-yl]sulfonyl}benzene 
• 15575-04-9 decaprenol 
• 13190-97-1 solanesol 
• 68690-55-1 1-((2E,6E,10E,14Z,18E,22E,26E)-1-Benzyloxy-3,7,11,15,19,23,27,31-octamethyl-dotriaconta-2,6,10,14,18,22,26,30-octaene-9-sulfonyl)-4-methyl-benzene 
• 5905-42-0 all-trans-3,7,11,15,19,23,27,31-octamethyl-2,6,10,14,18,22,26,30-triacontaoctaen-1-ol 
• 68690-49-3 1-((2E,6E,10E,14Z,18E)-3,7,11,15,19,23-Hexamethyl-tetracosa-2,6,10,14,18,22-hexaene-1-sulfonyl)-4-methyl-benzene 
• 314739-90-7 Se-phenyl (E,E,E,E,E)-5,9,13,17,21-pentamethyl-23-[(tetrahydro-2H-pyran-2-yl)oxy]tricosa-5,9,13,17,21-pentaeneselenoate 
• 314739-83-8 Se-phenyl (E,E,E,E,E)-23-hydroxy-5,9,13,17,21-pentamethyltricosa-5,9,13,17,21-pentaeneselenoate 
• 229305-81-1 (E,E,E,E,E,E,E)-1-(benzyloxy)-3,7,11,15,19,23,27,31-octamethyl-9-(phenylthio)dotriaconta-2,6,10,14,18,22,26,30-octaene 
• 229305-89-9 Se-phenyl (E,E,E,E,E,E,E)-5,9,13,17,21,25,29-heptamethyl-31-[(tetrahydro-2H-pyran-2-yl)oxy]hentriaconta-5,9,13,17,21,25,29-heptaeneselenoate 
• 229305-90-2 Se-phenyl (E,E,E,E,E,E,E)-31-hydroxy-5,9,13,17,21,25,29-heptmethylhentriaconta-5,9,13,17,21,25,29-heptaeneselenoate 
• 229305-79-7 (E,E,E,E,E)-3,7,11,15,19,23-hexamethyl-1-(phenylthio)tetracosa-2,6,10,14,18,22-hexaene 

Relevant articles and documents

Biosynthesis of sesterterpenes, head-to-tail triterpenes, and sesquarterpenes in Bacillus clausii: Identification of multifunctional enzymes and analysis of isoprenoid metabolites

We performed functional analysis of recombinant enzymes and analysis of isoprenoid metabolites in Bacillus clausii to gain insights into the biosynthesis of rare terpenoid groups of sesterterpenes, head-to-tail triterpenes, and sesquarterpenes. We have identified an (all-E)-isoprenyl diphosphate synthase (E-IDS) homologue as a trifunctional geranylfarnesyl diphosphate (GFPP)/hexaprenyl diphosphate (HexPP)/heptaprenyl diphosphate (HepPP) synthase. In addition, we have redefined the function of a tetraprenyl-β-curcumene synthase homologue as that of a trifunctional sesterterpene/triterpene/sesquarterpene synthase. This study has revealed that GFPP, HexPP, and HepPP, intermediates of two isoprenoid pathways (acyclic terpenes and menaquinones), are biosynthesized by one trifunctional E-IDS. In addition, GFPP/HexPP and HepPP are the primary substrates for the biosynthesis of acyclic terpenes and menaquinone-7, respectively. Multifunctional terpene biosynthetic enzymes: Geranylfarnesyl diphosphate (GFPP), hexaprenyl diphosphate (HexPP), and heptaprenyl diphosphate (HepPP) are intermediates in two isoprenoid pathways and are biosynthesized by one trifunctional (all-E)-isoprenyl diphosphate synthase. GFPP/HexPP and HepPP are mainly utilized for the biosynthesis of acyclic terpenes and menaquinone-7, respectively.