18189-05-4

Usage

Uses

Used in Fragrance Industry:
Hexyl anthranilate is used as a fragrance ingredient for its sweet, floral scent, serving as a synthetic substitute for jasmine and orange blossom. It is valued for its long-lasting scent, making it ideal for use in various applications.
Used in Cosmetic Products:
In the cosmetic industry, hexyl anthranilate is used as a scent component to impart a pleasant aroma to products. Its enduring fragrance quality enhances the sensory experience of these products, contributing to their appeal.
Used in Perfumes:
Hexyl anthranilate is utilized as a fixative in perfumes, helping to extend the longevity of the fragrance and providing a sweet, floral note to the scent profile.
Used in Air Fresheners:
In air freshener products, hexyl anthranilate is used to deliver a long-lasting, pleasant aroma, improving the scent experience in various environments.
Used in Sunscreen and Tanning Lotions:
Hexyl anthranilate is used in sunscreen and tanning lotions to provide a tropical, pleasant aroma, enhancing the overall user experience and making the application of these products more enjoyable.
Due to its low toxicity and safety for use in consumer products, hexyl anthranilate is a popular choice for fragrance applications across various industries, ensuring a delightful scent experience while maintaining product safety.

InChI:InChI=1/C13H19NO2/c1-2-3-4-7-10-16-13(15)11-8-5-6-9-12(11)14/h5-6,8-9H,2-4,7,10,14H2,1H3

Upstream product

• 117375-30-1 2-nitrobenzoic acid 1-hexyl ester 
• 118-92-3 anthranilic acid 
• 111-27-3 hexan-1-ol 
• 552-16-9 ortho-nitrobenzoic acid 

Downstream Products

• 180132-98-3 2-(2-nitro-4-methoxycarbonylbenzoylamino)benzoic acid 1-hexyl ester 
• 196311-84-9 2-(2-nitrobenzoylamino)benzoic acid 1-hexyl ester 
• 180133-00-0 2-{2-[2-(2-hexanoylamino-4-methoxycarbonylbenzoylamino)benzoylamino]-4-methoxycarbonylbenzoylamino}benzoic acid 1-hexyl ester 
• 180133-01-1 2-{2-[2-(2-hexanoylamino-4-hydroxycarbonylbenzoylamino)benzoylamino]-4-hydroxycarbonylbenzoylamino}benzoic acid 1-hexyl ester 
• 180133-10-2 2-{2-[2-(2-nitro-4-methoxycarbonylbenzoylamino)benzoylamino]-4-methoxycarbonylbenzoylamino}benzoic acid 1-hexyl ester 
• 180133-11-3 2-{2-[2-(2-amino-4-methoxycarbonylbenzoylamino)benzoylamino]-4-methoxycarbonylbenzoylamino}benzoic acid 1-hexyl ester 
• 182301-30-0 2-[2-(2-nitrobenzoylamino)-4-methoxycarbonylbenzoylamino]benzoic acid 1-hexyl ester 
• 180133-09-9 2-[2-(2-aminobenzoylamino)-4-methoxycarbonylbenzoylamino]benzoic acid 1-hexyl ester 
• 180132-99-4 2-(2-amino-4-methoxycarbonylbenzoylamino)benzoic acid 1-hexyl ester 
• 180335-21-1 C₁₉H₂₃N₃O₂ 
• 657412-92-5 2,5-Bis-hexyloxy-N-(2-hexyloxycarbonyl-phenyl)-terephthalamic acid benzyl ester 
• 67836-75-3 2-(3,4-Dimethoxy-benzoylamino)-benzoic acid hexyl ester 

Relevant academic research and scientific papers

Synthesis, antimicrobial evaluation, ot-QSAR and mt-QSAR studies of 2-amino benzoic acid derivatives

A series of 2-amino benzoic acid derivatives (1-28) were synthesized and evaluated for their in vitro antimicrobial activity against the panel of Gram positive, Gram negative bacterial and fungal strains. The results of antimicrobial studies indicated that, in general, the synthesized compounds were found to be bacteriostatic and fungistatic in action. QSAR studies performed by the development of one target and multi target models indicated that multi-target model was effective in describing the antimicrobial activity as well demonstrated the effect of structural parameters viz. LUMO, 3χv and W on antimicrobial activity of 2-amino benzoic acid derivatives. Springer Science+Business Media, LLC 2010.

Oligoanthranilamides. Non-peptide subunits that show formation of specific secondary structure

A family of novel oligomers based on the anthranilamide nucleus has been prepared and shown to form well-defined secondary structural features. 1H NMR and X-ray crystallographic techniques have demonstrated that intramolecular hydrogen bonds play a key role in stabilizing both linear sheet and helical conformational forms.

Steric effects in acid-catalyzed decomposition and base-catalyzed cyclization of 1-(2-alkoxycarbonyl-phenyl)-3-phenyltriazenes

Eight derivatives of 1-(2-alkoxycarbonylphenyl)-3-phenyltriazene (R = methyl, ethyl, propyl, isopropyl, butyl, isobutyl, hexyl, and allyl) have been synthesized and their UV-VIS, IR, 1H and 13C NMR spectra measured. The NMR spectra have been interpreted in detail. The kinetics of acid-catalyzed decomposition and base-catalyzed cyclization of the title compounds have been measured in 52.1% w/w methanol at 25.0 °C. The unit reaction order has been verified and the cyclization product has been identified. The pH-profiles obtained have been used to calculate the catalytic rate constants kA (acid-catalyzed decomposition) and kB (base-catalyzed cyclization) of all the derivatives; the constants have been interpreted with regard to inductive and steric effects. The catalytic rate constant kA has been found to be independent of the substituents. The catalytic rate constant kB depends statistically significantly upon both inductive and steric effects, the sensitivity to the former being more significant. The experimental results and their interpretation confirm the base-catalyzed cyclization mechanism with formation of tetrahedral intermediate as the rate-limiting step.