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Undec-10-en-1-amine

Base Information Edit
  • Chemical Name:Undec-10-en-1-amine
  • CAS No.:62595-52-2
  • Molecular Formula:C11H23N
  • Molecular Weight:169.31
  • Hs Code.:
  • European Community (EC) Number:870-286-7
  • DSSTox Substance ID:DTXSID80472084
  • Nikkaji Number:J97.653I
  • Mol file:62595-52-2.mol
Undec-10-en-1-amine

Synonyms:Undec-10-en-1-amine;62595-52-2;1-AMINO-10-UNDECENE;1-aminoundec-10-ene;10-Undecen-1-amine;aminoundec-10-ene;undec-10-enyl amine;11-aminoundec-1-ene;SCHEMBL132137;AMY6111;DTXSID80472084;PYGHKJQHDXSHES-UHFFFAOYSA-N;AKOS006292689;AS-75704;CS-0068719;E85573;EN300-317676;A904401

Suppliers and Price of Undec-10-en-1-amine
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
  • GFS CHEMICALS
  • 1-AMINO-10-UNDECENE
  • 10 G
  • $ 3400.40
  • American Custom Chemicals Corporation
  • 1-AMINO-10-UNDECENE 97.00%
  • 0.5G
  • $ 1232.00
  • AK Scientific
  • Undec-10-en-1-amine
  • 1g
  • $ 985.00
Total 18 raw suppliers
Chemical Property of Undec-10-en-1-amine Edit
Chemical Property:
  • Melting Point:85-86 °C 
  • Refractive Index:1.4487 
  • Boiling Point:238.999 °C at 760 mmHg 
  • PKA:10.67±0.10(Predicted) 
  • Flash Point:89.086 °C 
  • PSA:26.02000 
  • Density:0.811 g/cm3 
  • LogP:3.95220 
  • XLogP3:3.8
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:9
  • Exact Mass:169.183049738
  • Heavy Atom Count:12
  • Complexity:89
Purity/Quality:

98%,99%, *data from raw suppliers

1-AMINO-10-UNDECENE *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C=CCCCCCCCCCN
Technology Process of Undec-10-en-1-amine

There total 3 articles about Undec-10-en-1-amine 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 L-alanin; pyridoxal 5'-phosphate; alcohol dehydrogenase from Escherichia coli; amine transaminase from Chromobacterium violaceum; flavin adenine dinucleotide; In dimethyl sulfoxide; at 25 ℃; for 1.5h; pH=7; Enzymatic reaction;
DOI:10.1002/cctc.201701804
Guidance literature:
Multi-step reaction with 2 steps
1: disodium ethylenediamine tetraacetic acid; fatty acid decarboxylase cytochrome P450 OleT from Jeotgalicoccus sp. ATCC 8456; Flavin mononucleotide / dimethyl sulfoxide / 4 h / 25 °C / pH 7.5 / Irradiation; Enzymatic reaction
2: alcohol dehydrogenase from Escherichia coli; amine transaminase from Chromobacterium violaceum; L-alanin; flavin adenine dinucleotide; pyridoxal 5'-phosphate / dimethyl sulfoxide / 1.5 h / 25 °C / pH 7 / Enzymatic reaction
With L-alanin; pyridoxal 5'-phosphate; alcohol dehydrogenase from Escherichia coli; amine transaminase from Chromobacterium violaceum; fatty acid decarboxylase cytochrome P450 OleT from Jeotgalicoccus sp. ATCC 8456; disodium ethylenediamine tetraacetic acid; Flavin mononucleotide; flavin adenine dinucleotide; In dimethyl sulfoxide;
DOI:10.1002/cctc.201701804
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