10-Azaniumyldecanoate

Base Information

• Chemical Name: 10-Azaniumyldecanoate
• CAS No.: 13108-19-5
• Molecular Formula: C10H21 N O2
• Molecular Weight: 187.282
• Hs Code.: 2922499990
• Mol file: 13108-19-5.mol

Synonyms:

Chemical Property of 10-Azaniumyldecanoate

Chemical Property:

• Vapor Pressure: 6.91E-05mmHg at 25°C
• Melting Point: 177 °C
• Boiling Point: 319.8°Cat760mmHg
• PKA: 4.78±0.10(Predicted)
• Flash Point: 147.2°C
• PSA: 63.32000
• Density: 0.975g/cm³
• LogP: 2.85080
• Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
• XLogP3: -0.9
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 8
• Exact Mass: 187.157228913
• Heavy Atom Count: 13
• Complexity: 121

Purity/Quality:

98%Min ^*data from raw suppliers

10-AminodecanoicAcid ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C(CCCCC(=O)[O-])CCCC[NH3+]

Technology Process of 10-Azaniumyldecanoate

There total 30 articles about 10-Azaniumyldecanoate 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: 100.0%

10-bromodecanoic acid (50530-12-6) → 10-aminodecanoic acid (13108-19-5)

Guidance literature:

With ammonium hydroxide; In water; at 20 ℃; for 24h;

DOI:10.1021/ja903292v

Reference yield:

11-hydroxyimino-triacontanoic acid (103799-79-7) + sulfuric acid (7664-93-9) → 1-nonadecanamine (n-nonadecylamine) (14130-05-3) + 10-aminodecanoic acid (13108-19-5) + undecanedioic acid (1852-04-6) + Arachidic acid (506-30-9)

Guidance literature:

Erhitzen des Reaktionsprodukts mit konz. HCl auf 180grad;

Reference yield:

→ azelaic acid (123-99-9,26776-28-3) + 10-aminodecanoic acid (13108-19-5)

Guidance literature:

und Erwaermen des oeligen Oxims der κ-Oxo-pentadecylsaeure mit konz.Schwefelsaeure und nachfolgendes Erhitzen mit 48prozentiger Bromwasserstoffsaeure im Rohr auf 170grad;

upstream raw materials:

azelaic acid

azacycloundecan-2-one

10-amino-decanenitrile

10,10-dichloro-dec-9-enylamine

Downstream raw materials:

10-(N-tert-butoxycarbonyl)aminodecanoic acid

(10-aminodecanoyl)-Ser-Lys-2-cyclohexylethylamide

(11-Methacryloyl-amino)undecansaeure

10-<(phenylmethoxy)carbonylamino>decanoic acid

Refernces

• 1、 Jung, Hyunsang,Kim, Byung-Gee,Kim, Ye Chan,Park, Beom Gi,Patil, Mahesh D.,Sarak, Sharad,Yoo, Hee-Wang,Yun, Hyungdon. "Multi-enzymatic cascade reactions with Escherichia coli-based modules for synthesizing various bioplastic monomers from fatty acid methyl esters?". supporting information. p. 2222 - 2231. Retrieved 2022/04/03.
• 2、 Sung, Sihyong,Jeon, Hyunwoo,Sarak, Sharad,Ahsan, Md Murshidul,Patil, Mahesh D.,Kroutil, Wolfgang,Kim, Byung-Gee,Yun, Hyungdon. "Parallel anti-sense two-step cascade for alcohol amination leading to ω-amino fatty acids and α,ω-diamines". supporting information. p. 4591 - 4595. Retrieved 2018/10/23.