85655-98-7

Usage

Uses

Used in Fragrance Industry:
3-HEXYN-1,6-DIOL is used as a fragrance ingredient in perfumes and cosmetics for its pleasant, floral scent, enhancing the overall aroma of these products.
Used in Food and Beverage Industry:
In the food and beverage industry, 3-HEXYN-1,6-DIOL is used as a flavoring agent to impart a distinct taste and aroma to various products, contributing to their sensory appeal.
Used in Personal Care Industry:
3-HEXYN-1,6-DIOL is utilized in personal care products due to its antibacterial properties, which help maintain hygiene and prevent the growth of harmful microorganisms on the skin and hair.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 3-HEXYN-1,6-DIOL is employed for its antibacterial properties, which can be beneficial in the development of medications and treatments that require antimicrobial action.

InChI:InChI=1/C6H10O2/c7-5-3-1-2-4-6-8/h7-8H,3-6H2

Upstream product

• 104178-62-3 6-<(tetrahydro-2H-pyran-2-yl)oxy>-3-hexyn-1-ol 
• 10229-11-5 4-phenyl-but-3-yn-1-ol 
• 75-21-8 oxirane 
• 927-74-2 3-Butyn-1-ol 
• 40365-61-5 2-(but-3-yn-1-yloxy)tetrahydropyran 

Downstream Products

• 629-11-8 1,6-hexanediol 
• 71655-17-9 (E)-3-hexen-1,6-diol 
• 5557-87-9 3,4-pentadiene-1-ol 
• 106-99-0 buta-1,3-diene 
• 1079308-79-4 (E)-N,N'-bis(tert-butyloxycarbonyl)-N,N'-bis[(4-methylphenyl)sulfonyl]-3-hexene-1,6-diamine 
• 244252-53-7 C₄₂H₃₈P₂ 
• 1001412-50-5 C₂₄H₂₈ClN₃O₄ 

Relevant academic research and scientific papers

NOVEL SYNTHETIC BINDING PAIRS AND USES THEREOF

Cucurbituril assemblies, polyamine structures capable of binding thereto, affinity pairs of cucurbituril assemblies and such polyamine structures and methods utilizing same are disclosed.

Silanol-molybdenum hexacarbonyl as a new efficient catalyst for metathesis of functionalised alkynes under microwave irradiation

The catalytic mixture based on Mo(CO)6 was re-examined in the metathesis of 4-methoxytolan. Silanols (4) or (5) were found to be very active as co-catalysts. The metathesis of functional alkynes was convenient and rapidly achieved in octane as solvent under microwave irradiation in a resonance cavity.

Elimination Instead of Rearrangement in Sulfur-Containing C12 Rings

Syntheses of dithiacyclotetradecadiyne 13 and -diene 26 as well as thiacyclotridecatriene 36 are reported.Stevens rearrangement and elimination of sulfur from the methyl sulfonium salts 20 and 37 in order to obtain 1,4,7,10-cyclododecatetraene (1) or dienediyne 2 have not been successful; instead, only the ring-opened methyl thioethers 23 and 39 have been isolated.

HOMOGENEOUS METATHESIS OF FUNCTIONALISED ACETYLENES

The first examples of functionalised acetylenes metathesis are described: (1) using molybdenum carbonyl-phenol complexes gave the expected tolane (2) and disubstituted acetylene (3).