1-Phenyl-2-butanamine hydrochloride

Base Information

Chemical Name:1-Phenyl-2-butanamine hydrochloride
CAS No.:20735-15-3
Molecular Formula:C10H15N · HCl
Molecular Weight:185.69
Hs Code.:
European Community (EC) Number:693-472-8
ChEMBL ID:CHEMBL540053
DSSTox Substance ID:DTXSID80508458
Mol file:20735-15-3.mol

Synonyms:1-PHENYL-2-BUTANAMINE HYDROCHLORIDE;20735-15-3;1-phenylbutan-2-amine;hydrochloride;2-Amino-1-phenylbutane (hydrochloride);Benzeneethanamine, alpha-ethyl-, hydrochloride (1:1);1-Benzyl-Propylamine HCl;CHEMBL540053;SCHEMBL8734599;DTXSID80508458;1-phenylbutan-2-amine hydrochloride;PD018699;1-Phenylbutan-2-amine--hydrogen chloride (1/1);J-013564

Suppliers and Price of 1-Phenyl-2-butanamine hydrochloride

Supply Marketing:

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

Sigma-Aldrich
1-Phenyl-2-butanamine hydrochloride
5mg
$ 143.00

Cayman Chemical
2-Amino-1-phenylbutane (hydrochloride) ≥98%
10mg
$ 221.00

Cayman Chemical
2-Amino-1-phenylbutane (hydrochloride) ≥98%
5mg
$ 118.00

Cayman Chemical
2-Amino-1-phenylbutane (hydrochloride) ≥98%
1mg
$ 49.00

American Custom Chemicals Corporation
1-PHENYL-2-BUTANAMINE HYDROCHLORIDE 95.00%
5MG
$ 708.30

AK Scientific
1-Phenyl-2-butanamine hydrochloride
5mg
$ 259.00

Total 30 raw suppliers

Chemical Property of 1-Phenyl-2-butanamine hydrochloride

Chemical Property:

Melting Point:143-144°C
PSA：26.02000
LogP:3.46870
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:3
Exact Mass:185.0971272
Heavy Atom Count:12
Complexity:95

Purity/Quality:

99% ^*data from raw suppliers

1-Phenyl-2-butanamine hydrochloride ^*data from reagent suppliers

Safty Information:

Pictogram(s): Xn
Hazard Codes:Xn
Statements: 22-36
Safety Statements: 26

MSDS Files:

Useful:

Canonical SMILES:CCC(CC1=CC=CC=C1)N.Cl
Description Amphetamines are chemical compounds characterized by an α-methylphenethylamine base structure. D-amphetamine is a stimulant that binds the norepinephrine and dopamine transporters (EC50s = 7.1 and 24.8 nM, respectively). 2-Amino-1-phenylbutane is an amphetamine characterized by having an ethyl group in the alpha position. It has emerged as a potential recreational drug. This product is a mixture of the D and L isomers. The D isomer of 1-Phenyl-2-butanamine hydrochloride partially substitutes for D-amphetamine in an animal discrimination analysis, suggesting that it weakly mimicks the signaling and stimulant properties of D-amphetamine. This product is intended for forensic and research applications.

Technology Process of 1-Phenyl-2-butanamine hydrochloride

There total 3 articles about 1-Phenyl-2-butanamine hydrochloride 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:

: 5368-18-3
1-phenyl-2-butanone oxime

: 20735-15-3
1-Phenyl-2-aminobutan-hydrochlorid

Guidance literature:: With hydrogenchloride; hydrogen; palladium on activated charcoal;

Reference yield:

: 1007-32-5
benzyl ethyl ketone

: 20735-15-3
1-Phenyl-2-aminobutan-hydrochlorid

Guidance literature:: Multi-step reaction with 2 steps

1: NH₂OH

2: H₂, HCl / Pd/C

With hydrogenchloride; hydrogen; hydroxylamine; palladium on activated charcoal;

Reference yield:

: 1589-82-8
phenylmagnesium bromide

: 20735-15-3
1-Phenyl-2-aminobutan-hydrochlorid

Guidance literature:: Multi-step reaction with 3 steps

2: NH₂OH

3: H₂, HCl / Pd/C

With hydrogenchloride; hydrogen; hydroxylamine; palladium on activated charcoal;