55073-86-4

Usage

Uses

Used in Fragrance Industry:
2,2,5,5-tetramethylhexan-1-ol is used as a fragrance ingredient for its pleasant scent, contributing to the production of perfumes, soaps, and other personal care products.
Used in Flavor and Food Additive Industry:
This chemical compound is utilized in the manufacturing of flavors and food additives, enhancing the taste and aroma of various food products.
Used in Industrial Processes:
2,2,5,5-tetramethylhexan-1-ol serves as a solvent in a range of industrial applications, facilitating various chemical reactions and processes.
Safety Note:
It is crucial to handle 2,2,5,5-tetramethylhexan-1-ol with care, as it can cause irritation to the skin, eyes, and respiratory system if not properly managed.

Upstream product

• 60-29-7 diethyl ether 
• 7065-46-5 3,3-dimethylbutanoic acid chloride 
• 67-56-1 methanol 
• 692-48-8 (E)-2,2,5,5-tetramethylhex-3-ene 

Downstream Products

• 33175-59-6 2,3,5,5,-tetramethyl-2-hexene 
• 115858-18-9 2,3,5,5,-tetramethyl-1-hexene 
• 692-48-8 (E)-2,2,5,5-tetramethylhex-3-ene 
• 16747-42-5 2,2,4,5-tetramethyl-hexane 
• 25966-58-9 2.2.5.5.-Tetramethyl-3-hexyl-tosylat 

Relevant academic research and scientific papers

Photochemistry of Alkenes. 8. Sterically Congested Alkenes

A study of photobehavior of the sterically congested tri- and di-tert-butylethenes 9, 21, and 25 has afforded additional insights into the excited singlet state behavior of alkenes.In pentane solution the carbene-derived products 11, 12, 24, and 32 were formed, respectively.In methanol tri-tert-butylethene (9) afforded additionally ether 14 and the rearranged alkenes 15 and 16 derived from protonation of carbene intermediate 10. 1,1-Di-tert-butyl analogue 21 afforded no detectable ether or rearranged alkene products.However, irradiation in methanol-O-d resulted in incorporation of deuterium at the vinyl positions of 21 recovered after partial conversion, apparently from deuteration-deprotonation of carbene intermediate 22.By contrast, 1,2-di-tert-butyl isomer 25 afforded no products attributable to protonation of the corresponding carbene intermediate 23 but gave ether 35b via 1,2 addition of methanol across the double bond of 25, perhaps involving protonation of the highly polarizable orthogonal 1(?,?*) intermediate.