1653-35-6

Basic information

• Product Name: pentadecan-8-ol
• Synonyms: pentadecan-8-ol;8-Pentadecanol
• CAS NO: 1653-35-6
• Molecular Formula: C₁₅H₃₂O
• Molecular Weight: 228.41398
• EINECS: 216-726-8
• Mol File: 1653-35-6.mol
• Article Data: 13

Chemical Properties

• Melting Point: 53.5-54.3 °C(Solv: ethyl acetate (141-78-6))
• Boiling Point: 300.24°C (estimate)
• Flash Point: 114.7°C
• Appearance: /
• Density: 0.8221 (estimate)
• Vapor Pressure: 0.000229mmHg at 25°C
• Refractive Index: 1.4249 (estimate)
• PKA: 15.36±0.20(Predicted)
• CAS DataBase Reference: pentadecan-8-ol(CAS DataBase Reference)
• NIST Chemistry Reference: pentadecan-8-ol(1653-35-6)
• EPA Substance Registry System: pentadecan-8-ol(1653-35-6)

Safety Data

• Hazardous Substances Data: 1653-35-6(Hazardous Substances Data)

Usage

General Description

Pentadecan-8-ol is a chemical compound that belongs to the class of alcohols, specifically the pentadecanol isomers. It is also known by the IUPAC name 8-Pentadecanol. With a molecular formula of C15H32O, pentadecan-8-ol is a white solid with a molecular weight of 220.41 g/mol. It is primarily used as a raw material in the production of various products such as surfactants, lubricants, and fragrances. Pentadecan-8-ol has also been studied for its potential antimicrobial and anti-inflammatory properties, making it of interest in the development of pharmaceutical and cosmetic products. Additionally, it is used in the synthesis of various organic compounds in the chemical industry. Overall, pentadecan-8-ol is a versatile chemical with diverse applications in different sectors.

InChI:InChI=1/C15H32O/c1-3-5-7-9-11-13-15(16)14-12-10-8-6-4-2/h15-16H,3-14H2,1-2H3

Upstream product

• 124-13-0 Octanal 
• 13125-66-1 n-heptylmagnesium bromide 
• 109-94-4 formic acid ethyl ester 
• 818-23-5 8-Pentadecanon 
• 107-31-3 Methyl formate 
• 200886-71-1 N-methoxy-N-methyloctanamide 
• 111-64-8 n-octanoic acid chloride 
• 111-25-1 1-bromo-hexane 
• 124-07-2 Octanoic acid 
• 629-04-9 1-Bromoheptane 
• 190249-59-3 8-Pentadecanol acetic acid ester 
• 555-31-7 aluminum isopropoxide 
• 64-17-5 ethanol 
• 111-87-5 octanol 

Downstream Products

• 15430-98-5 7-pentadecene 
• 818-23-5 8-Pentadecanon 
• 619-38-5 2-heptyl-nonanoic acid 
• 1093649-42-3 1-heptyl-1-(4-methoxyphenyl)octane 
• 796870-68-3 8-Pentadecanyl diphenyl phosphate 
• 55668-09-2 8-methylenepentadecane 
• 629-62-9 pentadecane 
• 18618-64-9 pentadecan-8-amine 

Relevant articles and documents

Synthesis and antimicrobial activity of symmetrical two-tailed dendritic tricarboxylato amphiphiles

Two series of water-soluble, symmetrical two-tailed homologous dendritic amphiphiles-R2NCONHC((CH2)2COOH)3, 2(n,n), and R2CHNHCONHC((CH2)2COOH)3, 3(n,n), where R = n-CnH2n+1-were synthesized and compared to R″NHCONHC((CH2)2COOH)3, 1(n), R″ = n-CnH2n+1, to determine whether antimicrobial activity was influenced by total or individual alkyl chain lengths, and whether antimicrobial activity depends on hydrophobicity or tail topology (one or two). In a broad screen of 11 microorganisms, 2(n,n) and 3(n,n) generally displayed higher minimal inhibitory concentrations (MICs) than 1(n) against growth as measured by broth microdilution assays. Chain-length specificity was observed against Candida albicans as 1(16), 2(8,8), and 3(8,8) showed the lowest MIC in their respective series. The one case where two-tailed compounds displayed the lowest MICs-3(10,10), 15 μM; 3(11,11), 7.2 μM; and 3(12,12), 6.9 μM-was against Cryptococcus neoformans.

COMPOUNDS USEFUL IN HIV THERAPY

The invention relates to compounds of Formula (I), salts thereof, pharmaceutical compositions thereof, as well as methods of treating or preventing HIV in subjects.

IONIZABLE CATIONIC LIPID FOR RNA DELIVERY

What is described is a compound of formula I consisting of a compound in which R1 is a branched chain alkyl consisting of 10 to 31 carbons; R2 is a linear alkyl, alkenyl, or alkynyl consisting of 2 to 20 carbons; L1 and L2 are the same or different, each a linear alkylene of 1 to 20 carbons or a linear alkenylene of 2 to 20 carbons; X1 is S or O; R3 is a linear or branched alkylene consisting of 1 to 6 carbons; and R4 and R5 are the same or different, each a hydrogen or a linear or branched alkyl consisting of 1 to 6 carbons; or a pharmaceutically acceptable salt thereof.

Synthesis and characterization of mesogenic triphenylene-perylene dyads with phenoxy-alkoxy linkers

Three novel triphenylene-perylene dyads with phenoxy-alkoxy linkers (PDI-OPhO-Cn-O- TP6, n = 6, 8, 10) have been synthesized and characterized by FT-IR, MS, 13C, and 1H NMR. The mesomorphic properties of these compounds were investigated by polarizing optical microscopy (POM) and differential scanning calorimetry (DSC). It was found that the dyads (PDI-OPhO-Cn-O-TP6, n = 6, 8) only showed thermotropic columnar mesophase in the heating process, while the dyad (PDI-OPhO-C10-O-TP6) showed enantiotropic columnar mesophase in both heating and cooling processes.