85655-98-7

Basic information

• Product Name: 3-HEXYN-1,6-DIOL
• Synonyms: TIMTEC-BB SBB009092;3-HEXYN-1,6-DIOL;3-HEXYNE-1,6-DIOL;3-HEXYN-1,6-DIOL, 97%,
• CAS NO: 85655-98-7
• Molecular Formula: C₆H₁₀O₂
• Molecular Weight: 114.14
• Mol File: 85655-98-7.mol
• Article Data: 5

Chemical Properties

• Melting Point: 80-80.5 °C(Solv: benzene (71-43-2))
• Boiling Point: 264.9 °C at 760 mmHg
• Flash Point: 131.8 °C
• Appearance: /
• Density: 1.077 g/cm³
• Vapor Pressure: 0.00131mmHg at 25°C
• Refractive Index: 1.495
• PKA: 14.02±0.10(Predicted)
• CAS DataBase Reference: 3-HEXYN-1,6-DIOL(CAS DataBase Reference)
• NIST Chemistry Reference: 3-HEXYN-1,6-DIOL(85655-98-7)
• EPA Substance Registry System: 3-HEXYN-1,6-DIOL(85655-98-7)

Safety Data

• Hazardous Substances Data: 85655-98-7(Hazardous Substances Data)

Usage

General Description

3-HEXYN-1,6-DIOL is a chemical compound with the formula C6H10O2. It is also known as 3-hexyn-1,6-diol and is classified as an alkyne alcohol. 3-HEXYN-1,6-DIOL is a colorless liquid with a mild, floral odor and is used in various applications, including as a fragrance ingredient in perfumes and cosmetics. It is also used as a flavoring agent in food and beverages. Additionally, 3-HEXYN-1,6-DIOL has antibacterial properties and is used in personal care products and pharmaceuticals. Overall, this chemical compound has diverse applications in the fragrance, food, and personal care industries.

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 
• 75-21-8 oxirane 
• 927-74-2 3-Butyn-1-ol 
• 10229-11-5 4-phenyl-but-3-yn-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 
• 1079308-79-4 (E)-N,N'-bis(tert-butyloxycarbonyl)-N,N'-bis[(4-methylphenyl)sulfonyl]-3-hexene-1,6-diamine 
• 1001412-50-5 C₂₄H₂₈ClN₃O₄ 
• 244252-53-7 C₄₂H₃₈P₂ 
• 5557-87-9 3,4-pentadiene-1-ol 
• 106-99-0 buta-1,3-diene 

Relevant articles and documents

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.

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).