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14-Aminotetradecan-1-ol

Base Information Edit
  • Chemical Name:14-Aminotetradecan-1-ol
  • CAS No.:89307-03-9
  • Molecular Formula:C14H31NO
  • Molecular Weight:229.406
  • Hs Code.:
  • DSSTox Substance ID:DTXSID30553271
  • Wikidata:Q82433818
  • Mol file:89307-03-9.mol
14-Aminotetradecan-1-ol

Synonyms:14-aminotetradecan-1-ol;1-Tetradecanol, 14-amino-;89307-03-9;14-Aminotetradecanol;14-Amino-1-tetradecanol;SCHEMBL486854;DTXSID30553271;MFCD09923507;SY298682

Suppliers and Price of 14-Aminotetradecan-1-ol
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
Total 3 raw suppliers
Chemical Property of 14-Aminotetradecan-1-ol Edit
Chemical Property:
  • Boiling Point:336.5±15.0 °C(Predicted) 
  • PSA:46.25000 
  • Density:0.879±0.06 g/cm3(Predicted) 
  • LogP:4.31890 
  • XLogP3:4.4
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:13
  • Exact Mass:229.240564612
  • Heavy Atom Count:16
  • Complexity:117
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C(CCCCCCCO)CCCCCCN
Technology Process of 14-Aminotetradecan-1-ol

There total 1 articles about 14-Aminotetradecan-1-ol 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:
Guidance literature:
With pyridoxal 5'-phosphate; MATITNHMPTAELQALDAAHHLHPFSANNALGEEGTRVITRARGVWLNDSEGEEILDAMAGLWCVNIGYGRDELAEVAARQMRELPYYNTFFKTTHVPAIALAQKLAELAPGDLNHVFFAGGGSEANDTNIRMVRTYWQNKGQPEKTVIISRKNAYHGSTVASSALGGMAGMHAQSGLIPDVHHINQPNWWAEGGDMDPEEFGLARARELEEAILELGENRVAAFIAEPVQGAGGVIVAPDSYWPEIQRICDKYDILLIADEVICGFGRTGNWFGTQTMGIRPHIMTIAKGLSSGYAPIGGSIVCDEVAHVIGKDEFNHGYTYSGHPVAAAVALENLRILEEENILDHVRNVAAPYLKEKWEALTDHPLVGEAKIVGMMASIALTPNKASRAKFASEPGTIGYICRERCFANNLIMRHVGDRMIISPPLVITPAEIDEMFVRIRKSLDEAQAEIEKQGLMKSA; MIKAYAALEANGKLQPFEYDPGALGANEVEIEVQYCGVCHSDLSMINNEWGISNYPLVPGHEVVGTVAAMGEGVNHVEVGDLVGLGWHSGYCMTCHSCLSGYHNLCATAESTIVGHYGGFGDRVRAKGVSVVKLPKGIDLASAGPLFCGGITVFSPMVELSLKPTAKVAVIGIGGLGHLAVQFLRAWGCEVTAFTSSARKQTEVLELGAHHILDSTNPEAIASAEGKFDYIISTVNLKLDWNLYISTLAPQGHFHFVGVVLEPLDLNLFPLLMGQRSVSASPVGSPATIATMLDFAVRHDIKPVVEQFSFDQINEAIAHLESGKAHYRVVLSHSKN; nicotinamide adenine dinucleotide phosphate; benzylamine; In dimethyl sulfoxide; at 37 ℃; for 24h; pH=8; Solvent; Microbiological reaction; Enzymatic reaction;
DOI:10.1039/c8gc02122h
upstream raw materials:

1,14-tetradecanediol

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