40228-93-1

Usage

Uses

Used in Pharmaceutical Applications:
15-PPDA is used as a potential therapeutic agent for its anti-inflammatory and antioxidant properties, which may contribute to the treatment or management of various inflammatory and oxidative stress-related conditions.
Used in Cosmetic Applications:
In the cosmetic industry, 15-PPDA is utilized as an ingredient in skincare and beauty products due to its potential benefits for skin health, possibly including anti-aging and moisturizing effects, attributed to its fatty acid and phenyl group composition.
Used in Diagnostic and Biomarker Research:
15-PPDA is being investigated for its potential use as a biomarker or diagnostic tool for certain medical conditions, leveraging its unique structure and the possibility of its involvement in specific physiological or pathological processes.
Further research is essential to fully explore and understand the potential uses and benefits of 15-PPDA across different industries and applications.

InChI:InChI=1/C21H34O2/c22-21(23)19-15-10-8-6-4-2-1-3-5-7-9-12-16-20-17-13-11-14-18-20/h11,13-14,17-18H,1-10,12,15-16,19H2,(H,22,23)

Upstream product

• 104827-29-4 15-Phenyl-pentadecanenitrile 
• 156632-09-6 14-keto-15-phenyl-tetradecacarboxylic acid 
• 931-88-4 cis-Cyclooctene 
• 50889-29-7 (5-carboxypentyl)triphenylphosphonium bromide 
• 645-45-4 hydrocinnamic acid chloride 
• 536-74-3 phenylacetylene 
• 3344-70-5 1,12-dibromododecane 
• 156632-08-5 14-keto-15-phenyl-tetradecacarboxylic acid ethyl ester 
• 109318-79-8 (Z)-9-Phenyl-non-8-enal 
• 167990-16-1 9-phenylnon-8-en-1-ol 
• 184900-11-6 13-oxo-15-phenyl-pentadecanoic acid 
• 104827-28-3 (14-Bromo-tetradecyl)-benzene 
• 104827-27-2 14-bromo-1-phenyl-tetradec-1-yne 
• 3884-92-2 methyl 8-oxooctanoate 

Downstream Products

• 88336-99-6 ω-phenyl pentadecanoic acid methyl ester 
• 117240-14-9 15-phenyl-pentadecanoyl-chloride 
• 88337-00-2 methyl 15-(p-iodophenyl)pentadecanoate 
• 80479-93-2 15-(p-iodophenyl)pentadecanoic acid 

Relevant academic research and scientific papers

Synthesis and nematocidal activity of aralkyl- and aralkenylamides related to piperamide on second-stage larvae of Toxocara canis

Seventy-nine aralkyl- and aralkenylamides related to piperamides were synthesized and their nematocidal activity against second-stage larvae of dog roundworm, Toxocara canis, was examined. The activity was greatly dependent on the alkyl chain length and the nature of the amine moiety, but was scarcely affected by the presence or absence of double bond(s) in the chain. The alkyl chain lengths which showed the strongest activity in a series of homologues were m=11 for the pyrrolidine amides and m=13 for the N- methylpiperazine amides. Although piperamides (3,4-methylenedioxyphenyl homologues) showed the strongest activity among the homologues tested, methoxy substituent(s) on the aromatic ring did not have much effect on the activity. However, conversion of the methoxy group to a hydroxy group greatly decreased the activity and shortened the chain length giving the strongest activity. Calculated log P values of non-phenolic aryl-piperamides fell in the range from 3.5 to 4.5, whereas those of hydroxyphenyl-piperamides were smaller, suggesting that different mechanisms are involved in the nematocidal activity of phenolic and non-phenolic compounds.

Synthesis, lipophilicity studies and antibacterial properties of some novel quaternary ammonium salts

The synthesis of some novel quaternary ammonium salts, derivatives of 15- phenyl-decapentanoic acid, is described. Their lipophilicity was estimated applying the Hansch-Leo fragmental procedure and measured by means of reversed phase thin layer chromatography. All compounds were tested for their antibacterial activity against Gram positive and gram negative microorganisms. The less lipophilic compounds showed weak activity, mainly against gram positive microorganisms.

Methode de synthese d'acides gras marques substitues ou non en α et en β

2-Propyn-1-ol and the dibromides Br(CH2)nBr (n = 10-12) have been used as starting materials for the synthesis of α- and β-methyl-branched fatty acids (C16) labeled with 123I at the ω-position.The methyl groups are introduced through the use of the lithium salt of either propanoic or isobutyric acid.The synthesis of *IC6H5(CH2)14COOH and *IC6H5(CH2)12CH(CH3)CH2COOH have been achieved in the same way starting from phenylacetylene.In each case, the radioactive iodine atom is introduced by an I/*I exchange reaction.