(Z)-7-Hexadecenoic acid

Base Information

• Chemical Name: (Z)-7-Hexadecenoic acid
• CAS No.: 2416-19-5
• Molecular Formula: C16H30 O2
• Molecular Weight: 254.413
• Hs Code.: 2916190090
• DSSTox Substance ID: DTXSID00920496
• Nikkaji Number: J658.909J
• Wikidata: Q27116491
• Metabolomics Workbench ID: 1106
• Mol file: 2416-19-5.mol

Synonyms:(Z)-7-Hexadecenoic acid;2416-19-5;cis-7-Hexadecenoic Acid;(Z)-hexadec-7-enoic acid;7-Hexadecenoic acid, (Z)-;hypogeic acid;(7Z)-hexadecenoic acid;7Z-hexadecenoic acid;Hexadec-7-enoic acid;7-hexadecenoic acid;C16:1n-9;7Z-palmitoleic acid;(Z)-7-Hexadecenoate;hexadec-7Z-enoic acid;Z-7-Hexadecenoic acid;7(Z)-Hexadecenoic acid;(7Z)-hexadec-7-enoic acid;16:1 cis7;SCHEMBL410914;(7Z)-7-Hexadecenoic acid #;CHEBI:35465;DTXSID00920496;PJHOFUXBXJNUAC-KTKRTIGZSA-N;HMS3650E21;LMFA01030055;C16:1(n=9);SR-01000946779;J-015372;SR-01000946779-1;Q27116491

Chemical Property of (Z)-7-Hexadecenoic acid

Chemical Property:

• Vapor Pressure: 1.19E-06mmHg at 25°C
• Boiling Point: 374.8°Cat760mmHg
• PKA: 4.77±0.10(Predicted)
• Flash Point: 271.7°C
• PSA: 37.30000
• Density: 0.905g/cm³
• LogP: 5.32830
• XLogP3: 6.4
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 13
• Exact Mass: 254.224580195
• Heavy Atom Count: 18
• Complexity: 209

Purity/Quality:

99%+ ^*data from raw suppliers

(7Z)?-7-?Hexadecenoicacid ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCCCCCC=CCCCCCC(=O)O
• Isomeric SMILES: CCCCCCCC/C=C\CCCCCC(=O)O
• Uses: (7Z)?-7-?Hexadecenoic acid is a fatty acid that may be useful for determining the specific genus of a bacterial population present in a variety of natural environments.

Technology Process of (Z)-7-Hexadecenoic acid

There total 12 articles about (Z)-7-Hexadecenoic acid which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

12-deoxyphorbol-13-(7Z)-hexadecenoate → 16:1ω7c fatty acid (2416-19-5)

Guidance literature:

With potassium hydroxide; In ethanol; at 20 ℃; for 24h;

DOI:10.1080/14786419.2019.1616728

Reference yield:

palmitolic acid (629-57-2) → 16:1ω7c fatty acid (2416-19-5)

Guidance literature:

With quinoline; hydrogen; palladium on barium sulfate; In methanol;

DOI:10.1039/jr9630000775

Reference yield:

1-decyne (764-93-2) → 16:1ω7c fatty acid (2416-19-5)

Guidance literature:

Multi-step reaction with 2 steps

1: (i) LiNH₂, liq. NH₃, (ii) /BRN= 1749740/, THF

2: H₂, quinoline / Pd-BaSO₄ / methanol

With quinoline; hydrogen; palladium on barium sulfate; In methanol;

DOI:10.1039/jr9630000775

upstream raw materials:

palmitolic acid

1-decyne

6-bromohexanoic acid

trioleoylglycerol

Downstream raw materials:

Z-7-hexadecen-1-yl acetate

Δ7-hexadecenol

(Z)-7-hexadecanoic acid methyl ester