6750-34-1

Basic information

• Product Name: 3,7,11-TRIMETHYL-1-DODECANOL
• Synonyms: 3,7,11-TRIMETHYL-1-DODECANOL;Hexa-hydro-farnesol;NISTC6750341;1-DODECANOL,3,7,11-TRIMETHYL-;3,7,11-trimethyldodecan-1-ol
• CAS NO: 6750-34-1
• Molecular Formula: C₁₅H₃₂O
• Molecular Weight: 228.41
• Mol File: 6750-34-1.mol
• Article Data: 21

Chemical Properties

• Boiling Point: 279.2°C at 760 mmHg
• Flash Point: 122.7°C
• Appearance: /
• Density: 0.831g/cm³
• Vapor Pressure: 0.000495mmHg at 25°C
• Refractive Index: 1.443
• Storage Temp.: Refrigerator, under inert atmosphere
• Solubility: Chloroform (Sparingly), Methanol (Slightly)
• PKA: 15.13±0.10(Predicted)
• CAS DataBase Reference: 3,7,11-TRIMETHYL-1-DODECANOL(CAS DataBase Reference)
• NIST Chemistry Reference: 3,7,11-TRIMETHYL-1-DODECANOL(6750-34-1)
• EPA Substance Registry System: 3,7,11-TRIMETHYL-1-DODECANOL(6750-34-1)

Safety Data

• Hazardous Substances Data: 6750-34-1(Hazardous Substances Data)

Usage

Description

3,7,11-TRIMETHYL-1-DODECANOL is a fatty alcohol that is 1-dodecanol substituted by methyl groups at positions 3, 7, and 11. It is a metabolite observed in cancer metabolism.

Uses

Used in Pharmaceutical Industry:
3,7,11-TRIMETHYL-1-DODECANOL is used as a pharmaceutical candidate for cancer treatment due to its presence in cancer metabolism. It may have potential applications in developing targeted therapies or diagnostic tools for cancer detection and monitoring.
Used in Research and Development:
3,7,11-TRIMETHYL-1-DODECANOL is used as a research compound for studying the role of fatty alcohols in cancer metabolism and their potential as therapeutic targets or biomarkers for various types of cancer.
Used in Cosmetic Industry:
3,7,11-TRIMETHYL-1-DODECANOL may be used as an ingredient in cosmetic products for its emollient and moisturizing properties, helping to improve skin hydration and texture.
Used in Perfumery:
3,7,11-TRIMETHYL-1-DODECANOL can be used as a fragrance ingredient in perfumery due to its unique scent profile, contributing to the creation of various olfactory compositions.
Used in Flavor Industry:
3,7,11-TRIMETHYL-1-DODECANOL may be used as a flavoring agent in the food and beverage industry, providing a unique taste and enhancing the overall flavor profile of products.

InChI:InChI=1/C15H32O/c1-13(2)7-5-8-14(3)9-6-10-15(4)11-12-16/h13-16H,5-12H2,1-4H3

Upstream product

• 4602-84-0 farnesol 
• 61252-24-2 3,7,11-trimethyl-2E-dodecen-1-yl alcohol 
• 29548-30-9 farnesyl acetate 
• 37519-97-4 1-hydroxy-3,7,11-trimethyl-6,10-dodecadiene 
• 141-78-6 ethyl acetate 
• 105470-79-9 (3R,7R,5E)-3,7,11-trimethyldodecan-1-al 
• 73408-00-1 ((4R,8R)-4,8,12-trimethyl-tridec-1-en-t-yl)-benzene 
• 59983-90-3 (3R,7R)-3,7,11-trimethyl-dodecanoic acid ethyl ester 
• 59965-19-4 dihydro-(R)-(+)-β-citronellyl tosylate 
• 65527-98-2 (Ξ)-2-((S)-4-bromo-3-methyl-butoxy)-tetrahydro-pyran 
• 66261-43-6 (3R,7R)-1-chloro-3,7,11-trimethyl-dodecane 
• 66261-54-9 (3S,7S)-3,7,11-trimethyl-dodeca-4c,8c-dien-1-ol 
• 13955-73-2 (3R,7R)-3,7,11-trimethyldodecanoic acid 
• 99265-64-2 (R)-3,7,11-trimethyl-2E-dodecen-1-ol 

Downstream Products

• 1190-55-2 3R(+),7RS-3,7,11-trimethyldodecanoic acid 
• 59100-81-1 4-(3,7,11-Trimethyldodecyloxy)-benzoesaeure 
• 68985-16-0 tosylated farnesanol 
• 128075-80-9 fluorescein 3,7,11-trimethyldodecyl ester 
• 3891-98-3 2,6,10-trimethyldodecane 
• 649551-83-7 3-benzyloxy-2-(3,4,5-trimethoxy-phenyl)-7-(3,7,11-trimethyl-dodecyl)-chromen-4-one 
• 94828-15-6 hexahydrofarnesyl p-tolylsulfone 
• 94827-97-1 2-(5'-p-tosyl-phytyl)-3-methyl-1,4-dimethoxynaphthalene 
• 1189-36-2 3,7,11-trimethyldodec-1-ene 
• 502-69-2 6,10,14-Trimethyl-2-pentadecanon 
• 505-32-8 isophytol 
• 253686-88-3 (E)-3,7,11,15-tetramethylhexadec-2-en-1-ol 
• 105172-88-1 all-rac-5-hydroxy-2-(4',8',12'-trimethyltridecyl)-2,4,6,7-tetramethyl-2,3-dihydrobenzofuran 
• 118017-27-9 all-rac-5-(benzyloxy)-2-(4',8',12'-trimethyltridecenyl)-2,4,6,7-tetramethyl-2,3-dihydrobenzofuran 

Relevant articles and documents

Enantioselective Total Synthesis of the Archaeal Lipid Parallel GDGT-0 (Isocaldarchaeol)**

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Tocopherol side chain synthesis via asymmetric organocatalytic transfer hydrogenation and convenient measurement of stereoselectivity

An asymmetric synthetic route for 1-iodofarnesane, a key intermediate for tocopherol side chain synthesis, starting from (+)-(R)-citronellal was developed. 1-Iodofarnesane was prepared through eight steps in about 50% overall yield, and asymmetric transfe

ASYMMETRIC HYDROGENATION OF ALKENNES USING CHIRAL IRIDIUM COMPLEXES

The invention relates to the (stereoselective) hydrogenation of carbon-carbon double bonds in compounds having at least one such bond, e.g., isoprenoids, non-cyclic sesquiterpenes, tocomonoenols, tocodienols, tocotrienols or derivatives thereof, as well as to the (stereoselective) hydrogenation of parts/extracts of plant oils containing such tocotrienols or derivatives thereof, in the presence of a chiral Ir complex as the catalyst, whereby preferably one stereoisomer is manufactured in an excess.