5421-27-2

Usage

Uses

Used in Fragrance Industry:
Isobutyl undec-10-enoate is used as a fragrance ingredient for its ability to impart a pleasant, fresh, and uplifting scent to perfumes, colognes, and other scented products.
Used in Cosmetics:
Isobutyl undec-10-enoate is used as a scent enhancer in cosmetics to provide a light, sweet, and slightly citrusy aroma, enhancing the sensory experience of the products.
Used in Personal Care Products:
Isobutyl undec-10-enoate is used as a fragrance component in personal care products to add a refreshing and pleasant scent, making the products more appealing to users.
Used in Household Goods:
Isobutyl undec-10-enoate is used as a scent additive in household goods to impart a pleasant and fresh aroma, improving the overall sensory experience of the products.

InChI:InChI=1/C15H28O2/c1-4-5-6-7-8-9-10-11-12-15(16)17-13-14(2)3/h4,14H,1,5-13H2,2-3H3

Upstream product

• 78-83-1 2-methyl-propan-1-ol 
• 112-38-9 10-undecenoic acid 

Downstream Products

• 112-43-6 10-Undecen-1-ol 
• 259270-28-5 10-(fluoroethoxyphosphinyl)-N-(biotinamidopentyl)decanamide 

Relevant academic research and scientific papers

Synthesis, characterization, and evaluation of 10-undecenoic acid-based epithio derivatives as multifunctional additives

Novel epithio compounds from alkyl epoxy undecanoates (n-alkyl, C1, C4, and C6; isoalkyl, C3, C4, and C8) were synthesized using an ammonium thiocyanate in ionic liquid 1-methylimidazolium tetrafluoroborate/H2O (2:1) solvent system in 85-90% yields by gas chromatographic (GC) analysis. The synthesized products were characterized by 1H and 13C nuclear magnetic resonance spectroscopy, Fourier transform infrared spectroscopy (FTIR), gas chromatography, and GC mass spectral (GC-MS) analyses and evaluated for their antioxidant, extreme pressure (EP), and antiwear (AW) properties in three different base oils, namely, epoxy jatropha fatty acid n-butyl esters (EJB), di-2-ethylhexyl sebacate (DOS), and mineral oil (S-105). Among the synthesized products, n-butyl epithio undecanoate exhibited superior antioxidant property (229.2 °C) compared to butylated hydroxytoluene (BHT, 193.8 °C) in base oil DOS and comparable performance in EJB and S-105 base oils. All of the epithio derivatives exhibited significantly enhanced weld point for the base oils EJB and DOS at 2 wt % level and displayed moderate enhancement in S-105 base oil. Methyl epithio undecanoate at 0.6% concentration exhibited considerable improvement in the wear scar of DOS base oil. The synthesized epithio derivatives have potential as multifunctional additives in lubricant formulations.

HALOGEN PHOSPHONATE MONOESTERS

The present invention relates to detection, immobilization, and production of proteolytic antibodies using halogen phosphonate monoester probes, immobilizing reagents, and antigen conjugates.