cis-9-Octadecenal

Base Information

• Chemical Name: cis-9-Octadecenal
• CAS No.: 2423-10-1
• Molecular Formula: C18H34 O
• Molecular Weight: 266.467
• UNII: 753Z607472
• DSSTox Substance ID: DTXSID101016447
• Nikkaji Number: J110.771B
• Wikidata: Q27266333
• Pharos Ligand ID: 11Z7T5FHGDBB
• Metabolomics Workbench ID: 3631
• ChEMBL ID: CHEMBL486980
• Mol file: 2423-10-1.mol

Synonyms:cis-9-Octadecenal;Olealdehyde;2423-10-1;(Z)-octadec-9-enal;9Z-Octadecenal;9-Octadecenal, (9Z)-;9-Octadecenal, (Z)-;CHEMBL486980;753Z607472;Z-9-Octadecenal;(9Z)-9-Octadecenal;Oleylaldehyde;(Z)-olealdehyde;(Z)-9-Octadecenal;(9Z)-octadec-9-enal;(9Z)-9-Octadecenal #;9-OCTADECANAL (CIS);9-OCTADECENAL, CIS-;SCHEMBL597731;(Z)-9-OCTADECENYLALDEHYDE;DTXSID101016447;FEMA NO. 4059, Z-;BDBM50275297;LMFA06000238;MFCD31556108;UNII-753Z607472;AS-77798;Q27266333

Chemical Property of cis-9-Octadecenal

Chemical Property:

• Vapor Pressure: 1.92E-05mmHg at 25°C
• Melting Point: 33°C (estimate)
• Refractive Index: 1.4558
• Boiling Point: 362.6°Cat760mmHg
• Flash Point: 183.8°C
• PSA: 17.07000
• Density: 0.841g/cm³
• LogP: 6.22280
• Storage Temp.: Inert atmosphere,Store in freezer, under -20°C
• XLogP3: 7.2
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 15
• Exact Mass: 266.260965704
• Heavy Atom Count: 19
• Complexity: 196

Purity/Quality:

99% ^*data from raw suppliers

Cis-9-octadecenal 95% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCCCCCC=CCCCCCCCC=O
• Isomeric SMILES: CCCCCCCC/C=C\CCCCCCCC=O

Technology Process of cis-9-Octadecenal

There total 30 articles about cis-9-Octadecenal 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: 94.0%

oleyl alcohol (143-28-2,593-47-5,84286-21-5) → Oleic aldehyde (2423-10-1)

Guidance literature:

oleyl alcohol; With oxalyl dichloride; dimethyl sulfoxide; In dichloromethane; at -10 ℃; for 0.0833333h; Inert atmosphere;

In dichloromethane; at -10 ℃; for 0.25h; Inert atmosphere;

DOI:10.1039/d0nj02263b

Reference yield: 91.0%

oleoyl alcohol (143-28-2,593-47-5,84286-21-5) → Oleic aldehyde (2423-10-1)

Guidance literature:

With oxalyl dichloride; dimethyl sulfoxide; triethylamine; In dichloromethane; for 0.25h; cooling;

DOI:10.1016/j.chemphyslip.2005.02.008

Reference yield: 88.0%

C31H66O2Si2 → Oleic aldehyde (2423-10-1)

Guidance literature:

With hydrogenchloride; water; In tetrahydrofuran; Inert atmosphere;

DOI:10.1039/c3cc45349a

upstream raw materials:

(Z)-9-octadecenoyl chloride

oleyl alcohol

cis-Octadecenoic acid

(Z)-octadec-9-enoic hydrazide

Downstream raw materials:

C₃₆H₆₆O

1,1-diethoxy-octadec-9c-ene

Oelsaeurealdehyd-<4-(4-nitro-benzolazo)-benzoylhydrazon>

9-cis-octadecenal dimethyl acetal