1-Triacontanol

Base Information

• Chemical Name: 1-Triacontanol
• CAS No.: 593-50-0
• Molecular Formula: C30H62O
• Molecular Weight: 438.822
• Hs Code.: 29051990
• European Community (EC) Number: 209-794-5
• NSC Number: 405588,402492
• UNII: 767RD0E90B
• DSSTox Substance ID: DTXSID5029188
• Nikkaji Number: J6.767I
• Wikipedia: 1-Triacontanol
• Wikidata: Q4860821
• NCI Thesaurus Code: C87790
• Metabolomics Workbench ID: 3100
• ChEMBL ID: CHEMBL1079147
• Mol file: 593-50-0.mol

Synonyms:1-triacontanol;1-triacontanol, aluminum salt;triacontanol

Chemical Property of 1-Triacontanol

Chemical Property:

• Appearance/Colour: slightly beige flaky crystals
• Vapor Pressure: 1.01E-09mmHg at 25°C
• Melting Point: 86-87 °C(lit.)
• Refractive Index: 1.459
• Boiling Point: 443.338 °C at 760 mmHg
• PKA: 15.20±0.10(Predicted)
• Flash Point: 130.12 °C
• PSA: 20.23000
• Density: 0.842 g/cm³
• LogP: 10.92140
• Storage Temp.: 2-8°C
• Solubility.: Benzene (Slightly), Chloroform (Slightly, Heated)
• XLogP3: 14.9
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 28
• Exact Mass: 438.480066597
• Heavy Atom Count: 31
• Complexity: 288

Purity/Quality:

95%-98% ^*data from raw suppliers

Triacontanol ^*data from reagent suppliers

Safty Information:

• Safety Statements: 24/25

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Chemical Classes: Other Classes -> Alcohols and Polyols, Other
• Canonical SMILES: CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO
• Uses: It was reported to be a new naturally occurring plant-growth regulator. Present in plant cuticle waxes and in beeswax as the palmitate. It was reported to be a new naturally occurring plant-growth regulator. Present in plant cuticle waxes and in beeswax as the palmitate

Technology Process of 1-Triacontanol

There total 115 articles about 1-Triacontanol 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: 98.0%

12-Triaconten-1-ol (95855-73-5) → melissyl alcohol (593-50-0)

Guidance literature:

With hydrogen; platinum(IV) oxide; In methanol; toluene; for 6h;

Reference yield: 96.0%

methyl 1-triacontanoate (629-83-4) → melissyl alcohol (593-50-0)

Guidance literature:

With lithium aluminium tetrahydride; In tetrahydrofuran; 1.) -10 deg C -> room temperature, 1 h, 2.) room temperature, 4 h;

Reference yield: 95.0%

triacont-11-yn-1-ol (79162-67-7) → melissyl alcohol (593-50-0)

Guidance literature:

With hydrogen; palladium on activated charcoal; In tetrahydrofuran; for 4h;

upstream raw materials:

Ethyl tricontanoate

1-triacontyne

methyl 1-triacontanoate

n-triacontyl acetate

Downstream raw materials:

melissic acid

n-triacontyl acetate

1-triacosanal

triacontyl hexadecanoate

Refernces

• 1、 Cocker,Shaw. "". . p. 5194. Retrieved 1962.
• 2、 -. "A method for preparing high-purity triacontanol (by machine translation)". . . Retrieved 2017/09/01.
• 3、 -. "METHOD FOR THE PRODUCTION OF PRIMARY LONG-CHAIN ALCOHOLS". Page/Page column 11-12. . Retrieved 2010/02/15.