tert-Butylamine hydrobromide

Base Information

• Chemical Name: tert-Butylamine hydrobromide
• CAS No.: 60469-70-7
• Molecular Formula: C4H11 N . Br H
• Molecular Weight: 154.05
• Hs Code.: 2923900090
• European Community (EC) Number: 262-253-5
• NSC Number: 225071
• UNII: R857884BW2
• DSSTox Substance ID: DTXSID60209214
• Mol file: 60469-70-7.mol

Synonyms:tert-butylamine;tert-butylamine hydrobromide;tert-butylamine hydrochloride;tert-butylamine hydroiodide;tert-butylamine monolithium salt;tert-butylamine perchlorate;tert-butylamine sulfate (2:1);tert-butylamine thiocyanate;tert-butylamine, conjugate acid

Chemical Property of tert-Butylamine hydrobromide

Chemical Property:

• Vapor Pressure: 363mmHg at 25°C
• Melting Point: -72.65oC
• Boiling Point: 44.4°C at 760 mmHg
• PSA: 26.02000
• LogP: 2.40200
• Water Solubility.: Soluble in water
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 0
• Exact Mass: 153.01531
• Heavy Atom Count: 6
• Complexity: 25.1

Purity/Quality:

97% ^*data from raw suppliers

tert-Butylamine Hydrobromide ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(C)(C)N.Br
• Description: Bearing a?tert-butyl bulky group, t-butylammonium bromide (tBABr) is commonly used to alter perovskite structures to promote material solubility and device stability - by making them less sensitive to moisture (compared to 3D methylammonium-based perovskites).

Technology Process of tert-Butylamine hydrobromide

There total 4 articles about tert-Butylamine hydrobromide 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:

bromocyane (506-68-3) + tert-butylamine (75-64-9) → tert-butylamine hydrobromide (60469-70-7)

Guidance literature:

In diethyl ether; at 0 ℃; for 0.25h;

DOI:10.1016/j.tetlet.2005.12.083

Reference yield:

→ tert-butylamine hydrobromide (60469-70-7)

Guidance literature:

Reference yield:

→ 3-hydroxy-4-benzyloxy-alpha-tert-butylaminoacetophenone hydrochloride + tert-butylamine hydrobromide (60469-70-7)

Guidance literature:

upstream raw materials:

bromocyane

tert-butylamine

Downstream raw materials:

4-(2',5'-dimethoxy-3',4',6'-trimethylphenyl)-2-methyl-2-butenol