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2-n-Heptyl-4-quinolinol

* Please be kindly noted products are not for therapeutic use. We do not sell to patients.

Category Bioactive by-products
Catalog number BBF-01341
CAS
Molecular Weight 245.36
Molecular Formula C16H21NO

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Capabilities & Facilities

Fermentation Lab

4 R&D and scale-up labs

2 Preparative purification labs

Fermentation Plant

Semi pilot, pilot and industrial plant 4 Manufacturing sites 7 Production lines at pilot scale 100+ Reactors of 30-4000 L; 170+ reactors of 20 KL-30 KL; 24+ reactors of >100 KL 2 Hydrogenation reactors (200 L, 4Mpa and 1000L, 4Mpa)

Product Description

It is produced by the strain of Pseudomonas. It has activity against Candida albicans, Staphylococcus aureus, Vibrio anguillarum and V. Harveyi.

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IUPAC Name 2-heptyl-1,4-dihydroquinolin-4-ol
Canonical SMILES CCCCCCCC1=CC(C2=CC=CC=C2N1)O
InChI InChI=1S/C16H23NO/c1-2-3-4-5-6-9-13-12-16(18)14-10-7-8-11-15(14)17-13/h7-8,10-12,16-18H,2-6,9H2,1H3
InChI Key POWHEIUYDWIFET-UHFFFAOYSA-N
Antibiotic Activity Spectrum Gram-positive bacteria; Gram-negative bacteria; Yeast
1. Antibiotic metabolites from a marine pseudomonad
S J Wratten, M S Wolfe, R J Andersen, D J Faulkner Antimicrob Agents Chemother. 1977 Mar;11(3):411-4. doi: 10.1128/AAC.11.3.411.
An antibiotic-producing pseudomonad was isolated from a seawater sample from a La Jolla, Calif., tidepool. The pseudomonad produces two novel antibacterial compounds, 2-n-pentyl-4-quinolinol and 2-n-heptyl-4-quinolinol. It also synthesizes indole-3-carboxaldehyde, 6-bromoindole-3-carboxaldehyde, and the known antibiotic p-hydroxybenzaldehyde. Each of these compounds was identified by analysis of spectral data, and the structures were confirmed by synthesis or comparison with authentic samples.

Bio Calculators

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L

* Our calculator is based on the following equation:
Concentration (start) x Volume (start) = Concentration (final) x Volume (final)
It is commonly abbreviated as: C1V1 = C2V2

* Total Molecular Weight:
g/mol
Tip: Chemical formula is case sensitive. C22H30N4O c22h30n40
g/mol
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