(5-Bromopentyl)trimethylammonium bromide

Base Information

• Chemical Name: (5-Bromopentyl)trimethylammonium bromide
• CAS No.: 15008-33-0
• Molecular Formula: C8H19Br2N
• Molecular Weight: 289.054
• Hs Code.: 2923900090
• European Community (EC) Number: 625-200-0
• DSSTox Substance ID: DTXSID40455176
• ChEMBL ID: CHEMBL150123
• Mol file: 15008-33-0.mol

Synonyms:15008-33-0;(5-Bromopentyl)trimethylammonium bromide;5-Bromo-N,N,N-trimethylpentan-1-aminium bromide;5-Bromopentyl-trimethylammonium bromide;5-Bromopentyltrimethylammonium Bromide;5-bromopentyl(trimethyl)azanium;bromide;(5-Bromo-pentyl)-trimethyl-ammonium;MFCD00545102;(5-bromopentyl)trimethylazanium bromide;CHEMBL150123;D05KZH;SCHEMBL338814;DTXSID40455176;BCP32451;AC8016;AKOS015910844;(5-bromopen-tyl)trimethylammonium bromide;AS-70061;SY110604;FT-0663821;(5-BROMOPENTYL)TRIMETHYLAMMONIUMBROMIDE;5-Bromo-N,N,N-trimethylpentan-1-aminiumBromide;A884201;J-008657;1-Pentanaminium,5-bromo-N,N,N-trimethyl-,bromide(1:1);1-Pentanaminium, 5-bromo-N,N,N-trimethyl-, bromide (1:1)

Chemical Property of (5-Bromopentyl)trimethylammonium bromide

Chemical Property:

• Appearance/Colour: White Solid
• Melting Point: 141-143 °C(lit.)
• PSA: 0.00000
• LogP: -0.73820
• Storage Temp.: Inert atmosphere,Room Temperature
• Solubility.: DMSO (Slightly), Water (Slightly)
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 5
• Exact Mass: 288.98638
• Heavy Atom Count: 11
• Complexity: 75.8

Purity/Quality:

98%, ^*data from raw suppliers

5-Bromopentyl-trimethylammonium bromide ^*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

Useful:

• Canonical SMILES: C[N+](C)(C)CCCCCBr.[Br-]

Technology Process of (5-Bromopentyl)trimethylammonium bromide

There total 4 articles about (5-Bromopentyl)trimethylammonium bromide 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: 97.0%

1,5-dibromo-pentane (111-24-0) + trimethylamine (75-50-3) → (5-bromopentyl)trimethylammonium bromide (15008-33-0)

Guidance literature:

In tetrahydrofuran; for 72h; Ambient temperature;

DOI:10.1080/00397919908086244

Reference yield: 96.0%

→ (5-bromopentyl)trimethylammonium bromide (15008-33-0)

Guidance literature:

In tetrahydrofuran;

Reference yield: 71.0%

1,5-dibromo-pentane (111-24-0) + methylamine (74-89-5) → (5-bromopentyl)trimethylammonium bromide (15008-33-0)

Guidance literature:

In diethyl ether; at 0 ℃; for 0.0833333h; Inert atmosphere;

DOI:10.1021/acsmedchemlett.1c00455

upstream raw materials:

1,5-dibromo-pentane

trimethylamine

methylamine

Downstream raw materials:

1,3-dimethylalloxazine

TG-mPC₅C

Refernces

• 1、 Chai, Yunfeng,Xiong, Xingchuang,Yue, Lei,Jiang, You,Pan, Yuanjiang,Fang, Xiang. "Intramolecular Halogen Transfer via Halonium Ion Intermediates in the Gas Phase". . p. 161 - 167. Retrieved 2016.
• 2、 Tricot, Yves-M.,Porat, Ze'ev,Manassen, Joost. "Photoinduced and Redox-Induced Transmembrane Processes with Vesicle-Stabilized Colloidal Cadmium Sulfide and Multicharged Viologen Derivatives". . p. 3242 - 3248. Retrieved 1991.
• 3、 -. "Compositions containing ionic liquids and their uses, in particular in organic synthesis". Page/Page column 32. . Retrieved 2016/10/17.