1786-08-9

Usage

Uses

Used in Food and Beverage Industry:
FEMA 3661 is used as a humectant, solvent, and甜味剂 to enhance the taste, texture, and shelf life of various food and beverage products.
Used in Pharmaceutical Industry:
FEMA 3661 is used as a solvent and carrier for various pharmaceutical formulations, including liquid medications, tablets, and capsules, to improve their solubility, stability, and bioavailability.
Used in Cosmetics and Personal Care Industry:
FEMA 3661 is used as a humectant and emollient in various cosmetics and personal care products, such as lotions, creams, and shampoos, to provide moisture retention and improve skin hydration.
Used in Oral Care Industry:
FEMA 3661 is used as a humectant and甜味剂 in oral care products, such as toothpaste and mouthwash, to enhance their taste and provide moisture retention for oral health.
Used in Tobacco Industry:
FEMA 3661 is used as a humectant and甜味剂 in various tobacco products, such as e-liquids and moist snuff, to improve their taste and provide moisture retention for a better smoking experience.

InChI:InChI=1/C10H16O/c1-8(2)6-10-7-9(3)4-5-11-10/h4,6,10H,5,7H2,1-3H3

Upstream product

• 53834-70-1 (5E)-3-hydroxy-3,7-dimethyl-3-hydroxy-1,5,7-octatriene 
• 894806-15-6 (2Z,5E)-3,7-dimethyl-7-methoxyocta-2,5-dien-1-ol 
• 141-79-7 4-methyl-pent-3-en-2-one 
• 763-32-6 2-methyl-1-buten-4-ol 
• 107-86-8 3,3-dimethyl acrylaldehyde 
• 106-25-2 Nerol 
• 64661-54-7 6-hydroxy-2,6-dimethyl-octa-2,7-dien-4-one 
• 894806-14-5 (2Z)-6-bromo-3,7-dimethyl-7-methoxyoct-2-en-1-ol 
• 75654-19-2 3,7-Dimethyl-1,6-octadien-3,5-diol 

Downstream Products

• 36043-53-5 3,7,7-Trimethyl-cyclohepta-2,5-diene-1,4-dione 

Relevant academic research and scientific papers

Organic compounds

The use as fragrance ingredient of 4—methylene—2—(2—methylprop—1—enyl)—tetrahydropyran.

Functionalization of the naturally occurring linalool and nerol by the palladium catalyzed oxidation of their trisubstituted olefinic bonds

Linalool and nerol, bio-renewable terpenic alkenyl alcohols found in many essential oils, were selectively oxidized by molecular oxygen in the presence of the chloride-free Pd(OAc)2/p-benzoquinone catalytic system. An efficient dioxygen-coupled

PROCESS FOR THE PREPARATION OF CIS-ROSE OXIDE

The present invention relates to a process for the preparation of a composition enriched in cis-2-(2-methylprop-1-enyl)-4-methyltetrahydropyran, comprising the catalytic hydrogenation of 2-(2-methylprop-1-enyl)-4-methylenetetrahydropyran in the presence of hydrogen and a heterogeneous catalyst comprising ruthenium.

Process for preparation of nerol oxide

The present invention relates to a process for the synthesis of racemic nerol oxide i.e. 3,6-dihydro-4-methyl-2-[2-methyl-1-propenyl)-2H-pyran from monoterpene alcohol nerol i.e. cis-3,7-dimethylocta-2,6-diene-1-ol.

Odoriferous cyclic ethers via co-halogenation reaction: Facile preparation of nerol oxide, Florol, Florol methyl ether, and Pityol methyl ether

A series of odoriferous cyclic ethers, including nerol oxide (1), Floral (2), Floral methyl ether (3), and Pityol methyl ether (4b), were prepared by a versatile synthetic protocol based on co-halogenation with 1,3-dibromo-5,5-dimethylhydantoin (= 1,3-dibromo-5,5-dimethylimidazolidine-2,4- dione; DDH) as the key step. The methodology provides a facile access to important perfumery molecules from abundantly available monoterpene alcohols.

PROCESS FOR THE PREPARATION OF NEROL OXIDE

The present invention relates to a process for the synthesis of racemic nerol oxide i.e. 3,6-dihydro-4-methyl-2-[2-methyl-1-propenyl)-2H-pyran from monoterpene alcohol nerol i.e. cis-3,7-dimethylocta-2,6-diene-1-ol.

Structure and the Synthesis of Novel Constituents of Yudzu Peel Oil and Their Conversion to Related Monoterpenes

Two novel minor components isolated from yudzu peel oil were characterized as monoterpene β-ketols, 1 and 3, by their synthesis, and they were converted to related monoterpenes, dihydroneroloxide (9) neroloxide (10) and ho-trienol (11).