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Usage

Uses

Used in Fragrance Industry:
Isobornyl isobutyrate is used as a fragrance ingredient for its fresh, fruity, and floral scent, enhancing the olfactory experience of consumer products.
Used in Cosmetics and Personal Care Products:
Isobornyl isobutyrate is used as a scent enhancer in cosmetics, soaps, and shampoos, providing a pleasant aroma and ensuring the fragrance remains consistent over time due to its stability.
Used in Air Fresheners and Cleaning Agents:
Isobornyl isobutyrate is used as an odor neutralizer in air fresheners and cleaning agents, effectively covering up undesirable smells while imparting a pleasant scent to the environment.
Used in Household Products:
Isobornyl isobutyrate is utilized in various household products to add a fresh and appealing scent, improving the overall sensory experience for users.

InChI:InChI=1/C14H24O2/c1-9(2)12(15)16-11-8-10-6-7-14(11,5)13(10,3)4/h9-11H,6-8H2,1-5H3/t10-,11-,14+/m0/s1

Upstream product

• 464-45-9 endo-borneol 
• 79-31-2 isobutyric Acid 
• 464-41-5 bornyl chloride 
• 565-00-4 dl-camphene 
• 464-43-7 borneol 
• 97-72-3 2-Methylpropionic anhydride 
• 464-43-7 d-borneol 
• 24393-70-2 isoborneol 
• 79-30-1 isobutyryl chloride 
• 285128-02-1 (-)-[bis-(1S)-(-)-bornyl] 1,3-acetonedicarboxylate 
• 285128-05-4 di-(-)-bornyl 1,1,3,3-tetramethyl-1,3-acetonedicarboxylate 

Relevant academic research and scientific papers

Insight into the Mechanism of the Acylation of Alcohols with Acid Anhydrides Catalyzed by Phosphoric Acid Derivatives

Insight into the mechanism of a safe, simple, and inexpensive phosphoric acid (H3PO4)-catalyzed acylation of alcohols with acid anhydrides is described. The corresponding in situ-generated diacylated mixed anhydrides, unlike traditionally proposed monoacylated mixed anhydrides, are proposed as the active species. In particular, the diacylated mixed anhydrides act as efficient catalytic acyl transfer reagents rather than as Br?nsted acid catalysts simply activating acid anhydrides. Remarkably, highly efficient phosphoric acid (1-3 mol %)-catalyzed acylation of alcohols with acid anhydrides was achieved and a 23 g scale synthesis of an ester was demonstrated. Also, phosphoric acid catalyst was effective for synthetically useful esterification from carboxylic acids, alcohols, and acid anhydride. Moreover, with regard to recent developments in chiral 1,1′-bi-2-naphthol (BINOL)-derived phosphoric acid diester catalysts toward asymmetric kinetic resolution of alcohols by acylation, some phosphate diesters were examined. As a result, a 31P NMR study and a kinetics study strongly supported not only the acid-base cooperative mechanism as previously proposed by other researchers but also the mixed anhydride mechanism as presently proposed by us.

Preparation method of bornyl fatty acid

The invention relates to a preparation method of bornyl fatty acid. Natural borneol is used as a raw material and condenses with fatty acid under the condition of a condensing agent to obtain the bornyl fatty acid. According to the preparation method of the bornyl fatty acid, the used raw materials are cheap and easy to obtain, the reaction conditions are relatively mild, and the reaction yield ishigh.

Engineering reactions in crystalline solids: Radical pairs in crystals of dialkyl 1,3-acetonedicarboxylates

(Equation presented) Crystalline dialkyl 1,3-acetonedicarboxylates give dialkyl succinates in high chemical yields by combination of α-carbonyl radical pairs produced by photochemical decarbonylation. It is proposed that the solid-state reaction depends on the exothermicity of two consecutive bond cleavage processes. It is also suggested that the efficiency of radical formation in the solid state is determined by the effect of substituents on bond dissociation energies and radical-stabilization abilities.