Didecylamine

Base Information

• Chemical Name: Didecylamine
• CAS No.: 1120-49-6
• Molecular Formula: C20H43N
• Molecular Weight: 297.568
• Hs Code.: 2921199090
• European Community (EC) Number: 214-312-1,271-218-3
• UNII: 82R4O8EP59
• DSSTox Substance ID: DTXSID7061518
• Nikkaji Number: J97.656C
• Wikidata: Q27269348
• Mol file: 1120-49-6.mol

Synonyms:Didecylamine;1120-49-6;1-Decanamine, N-decyl-;di-n-Decylamine;N-decyldecan-1-amine;UNII-82R4O8EP59;82R4O8EP59;EINECS 214-312-1;EINECS 271-218-3;EC 214-312-1;68526-64-7;bis(decyl)amine;di-decylamine;Didecylamine, 98%;N,N-Didecylamine #;Armeen 2-10;Di-decylamine hydrochloride;SCHEMBL64526;N-DECYL-1-DECANAMINE;DTXSID7061518;N-decyldecan-1-amine hydrochloride;BBL011338;MFCD00048396;STL146428;AKOS005720745;AS-56349;CS-0152167;D0446;FT-0625177;D81864;A802475;W-109107;Q27269348

Chemical Property of Didecylamine

Chemical Property:

• Appearance/Colour: white solid
• Vapor Pressure: 9.56E-06mmHg at 25°C
• Melting Point: 38-40 °C (lit.)
• Refractive Index: 1.447
• Boiling Point: 372.5 °C at 760 mmHg
• PKA: 10.87±0.19(Predicted)
• Flash Point: 163.5 °C
• PSA: 12.03000
• Density: 0.809 g/cm³
• LogP: 7.24830
• Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
• Solubility.: Chloroform (Slightly), Ethyl Acetate (Slightly) , Hexanes (Slightly)
• XLogP3: 8.8
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 18
• Exact Mass: 297.339550376
• Heavy Atom Count: 21
• Complexity: 149

Purity/Quality:

99% ^*data from raw suppliers

Didecylamine ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xi
• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: CCCCCCCCCCNCCCCCCCCCC
• Uses: Didecylamine is a nitrogen containing organic building blocks. It is also shown to be used as a substrate for the growth of gram-negative Pseudomonas sp bacteria obtained from the activated sludge.

Technology Process of Didecylamine

There total 32 articles about Didecylamine 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: 96.0%

N-benzyl-N-decyldecan-1-amine → didecylamine (1120-49-6)

Guidance literature:

With palladium on activated charcoal; hydrogen; In ethanol;

Reference yield: 93.0%

n-Dodecylamine (124-22-1) → didecylamine (1120-49-6)

Guidance literature:

With NiCuFeO(x); In 5,5-dimethyl-1,3-cyclohexadiene; for 24h; Inert atmosphere; Sealed tube; Reflux;

DOI:10.1002/chem.201203417

Reference yield: 92.0%

1-aminodecane (2016-57-1) → didecylamine (1120-49-6)

Guidance literature:

With Co₂Rh₂/C; In toluene; at 180 ℃; for 6h; under 760.051 Torr; Autoclave; Inert atmosphere;

DOI:10.1002/adsc.201701522

upstream raw materials:

1-aminodecane

decyl chloride

1-bromo dodecane

decanamide

Downstream raw materials:

N,N-bis-decyl-lactamide

N-methyldidecylamine

(E)-2-benzylidenedecanal

4-didecylamino-2,6-dimethoxyphenyl-bis(4-dimethylamino-2,6-trimethoxyphenyl)carbenium chloride

Refernces

• 1、 Guyer et al.. "-". . p. 1649,1652,1653. Retrieved 1955.
• 2、 Furugen, Chikara,Ito, Naoya,Jiang, Jing,Park, Kwihwan,Sajiki, Hironao,Shimizu, Eisho,Yamada, Tsuyoshi. "Highly Selective Hydrogenative Conversion of Nitriles into Tertiary, Secondary, and Primary Amines under Flow Reaction Conditions". . . Retrieved 2021/12/13.
• 3、 Chung, Hyunho,Han, Seulgi,Chung, Young Keun,Park, Ji Hoon. "Conversion of Primary Amines to Symmetrical Secondary and Tertiary Amines using a Co-Rh Heterobimetallic Nanocatalyst". supporting information. p. 1267 - 1272. Retrieved 2018/02/12.