59640-02-7

Basic information

• Product Name: (6E,10E,14E,18E,22E,26E,30E,34E)-3,7,11,15,19,23,27,31,35,39-decamethyltetraconta-1,6,10,14,18,22,26,30,34,38-decaen-3-ol
• CAS NO: 59640-02-7
• Molecular Formula: C₅₀H₈₂O
• Molecular Weight: 699.1855
• Mol File: 59640-02-7.mol

Chemical Properties

• Boiling Point: 726.3°C at 760 mmHg
• Flash Point: 120.6°C
• Density: 0.888g/cm³
• Vapor Pressure: 2.34E-24mmHg at 25°C
• Refractive Index: 1.506
• CAS DataBase Reference: (6E,10E,14E,18E,22E,26E,30E,34E)-3,7,11,15,19,23,27,31,35,39-decamethyltetraconta-1,6,10,14,18,22,26,30,34,38-decaen-3-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (6E,10E,14E,18E,22E,26E,30E,34E)-3,7,11,15,19,23,27,31,35,39-decamethyltetraconta-1,6,10,14,18,22,26,30,34,38-decaen-3-ol(59640-02-7)
• EPA Substance Registry System: (6E,10E,14E,18E,22E,26E,30E,34E)-3,7,11,15,19,23,27,31,35,39-decamethyltetraconta-1,6,10,14,18,22,26,30,34,38-decaen-3-ol(59640-02-7)

Safety Data

• Hazardous Substances Data: 59640-02-7(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
(6E,10E,14E,18E,22E,26E,30E,34E)-3,7,11,15,19,23,27,31,35,39-decamethyltetraconta-1,6,10,14,18,22,26,30,34,38-decaen-3-ol is used as an active pharmaceutical ingredient for its potential therapeutic properties, leveraging its complex structure and unique chemical properties to target specific biological pathways.
Used in Perfumery Industry:
In the perfumery industry, (6E,10E,14E,18E,22E,26E,30E,34E)-3,7,11,15,19,23,27,31,35,39-decamethyltetraconta-1,6,10,14,18,22,26,30,34,38-decaen-3-ol is used as a fixative or scent component for its unique and long-lasting olfactory characteristics, adding depth and complexity to fragrances.
Used in Organic Chemistry Research:
(6E,10E,14E,18E,22E,26E,30E,34E)-3,7,11,15,19,23,27,31,35,39-decamethyltetraconta-1,6,10,14,18,22,26,30,34,38-decaen-3-ol is used as a subject of study in organic chemistry for understanding its synthesis, reactivity, and potential applications in creating new compounds with novel properties.

Upstream product

• 1826-67-1 vinyl magnesium bromide 

Downstream Products

• 20801-95-0 2-Hydroxy-3-methoxy-5-methyl-6-decaprenyl-1,4-benzochinon 
• 14599-49-6 2-Hydroxy-3-methoxy-6-methyl-5-decaprenyl-1,4-benzochinon 
• 15575-04-9 decaprenol 
• 303-98-0 ubidecarenone 
• 65085-29-2 2-((2Z,6E,10E,14E,18E,22E,26E,30E,34E)-3,7,11,15,19,23,27,31,35,39-decamethyl-tetraconta-2,6,10,14,18,22,26,30,34,38-decaenyl)-5,6-dimethoxy-3-methyl-[1,4]benzoquinone 
• 7200-27-3 5-demethoxyubiquinone-10 
• 21110-52-1 2-Methoxy-6-methyl-5-decaprenyl-1,4-benzochinon 
• 20801-87-0 2-Methoxy-6-methyl-3-decaprenyl-1,4-benzochinon 

Relevant articles and documents

Synthesis of coenzyme Q10, ubiquinone

Processes for the stereospecific synthesis of coenzyme Q10, ubiquinone, are disclosed; a semi synthetic procedure using solanesol derived from tobacco waste as the starting material. The process of the invention results in high yields of isometrically use

SYNTHESIS OF all-(E)-DECAPRENOL AND ITS 2Z ISOMER

C5-chain growth in the structure of natural solanesol, isolated from tobacco, was realized by a C3 + C2 scheme.Decaprenol was separated into isomers with respect to the newly formed double bond by column chromatography on silica gel.The isomeric compositi

Hypertension treating agent containing polyprenyl alcohol

This invention relates to a hypertension treating agent comprising a polyprenyl alcohol or an ester thereof of the general formula: STR1 wherein n represents an integer of 7-10 and A represents a group of the general formula: STR2 in which a and b each represent hydrogen or they may form a bond, or STR3 in which R represents hydrogen or --COR', R' being a saturated or unsaturated aliphatic hydrocarbon group of 1-17 carbon atoms; cyclohexyl group; unsubstituted phenyl group or phenyl group substituted with a halogen atom or a lower alkoxy group; (halogen atom-substituted phenoxy)-lower alkyl group; or pyridyl group.