Arbutamine Hydrochloride

Base Information

Chemical Name:Arbutamine Hydrochloride
CAS No.:125251-66-3
Molecular Formula:C₁₈H₂₃NO₄*ClH
Molecular Weight:353.846
Hs Code.:

Synonyms:1,2-Benzenediol,4-[(1R)-1-hydroxy-2-[[4-(4-hydroxyphenyl)butyl]amino]ethyl]-, hydrochloride(9CI); 1,2-Benzenediol,4-[1-hydroxy-2-[[4-(4-hydroxyphenyl)butyl]amino]ethyl]-, hydrochloride, (R)-;(-)-Arbutamine hydrochloride; Arbutamine hydrochloride; GP 2-121-3

Suppliers and Price of Arbutamine 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

American Custom Chemicals Corporation
ARBUTAMINE HYDROCHLORIDE 95.00%
5MG
$ 502.65

Total 2 raw suppliers

Chemical Property of Arbutamine Hydrochloride

Chemical Property:

Vapor Pressure:3.24E-14mmHg at 25°C
Melting Point:55-58°
Boiling Point:578.3°Cat760mmHg
Flash Point:195.1°C
PSA：92.95000
Density:1.262g/cm³
LogP:2.84020

Purity/Quality:

99% ^*data from raw suppliers

ARBUTAMINE HYDROCHLORIDE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of Arbutamine Hydrochloride

There total 9 articles about Arbutamine 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:

: 51-41-2
norepinephrine

: 123-72-8
butyraldehyde

: 125251-66-3
1-(3,4 dihydroxyphenyl)-2-(4-(4-hydroxyphenyl)butylamino)ethanol hydrochloride

Guidance literature:: With acetic acid; PtO₂; In methanol; dichloromethane;

Reference yield:

: 501-94-0
p-hydroxyphenethyl alcohol

: 125251-66-3
Arbutamine hydrochloride

Guidance literature:: Multi-step reaction with 9 steps

1: 96 percent / K₂CO₃ / methanol

2: 88 percent / Dess-Martin / CH₂Cl₂

3: 84 percent / tetrahydrofuran

4: 94 percent / H₂ / 10percent Pd-C / ethanol

5: 96 percent / NaH / dimethylformamide

6: 100 percent / LiOH / methanol; H₂O

7: 82 percent / DEPC, Et₃N / dimethylformamide / from 0 deg to RT

8: LiAlH₄ / diethyl ether / Heating

9: conc. MeOH / methanol; tetrahydrofuran / 0.5 h / Ambient temperature

With methanol; lithium hydroxide; lithium aluminium tetrahydride; hydrogen; sodium hydride; potassium carbonate; Dess-Martin periodane; triethylamine; diethyl dicarbonate; palladium on activated charcoal; In tetrahydrofuran; methanol; diethyl ether; ethanol; dichloromethane; water; N,N-dimethyl-formamide;
DOI:10.3987/com-97-s55

Reference yield:

: 40167-10-0
2-[4-(benzyloxy)phenyl]acetaldehyde

: 125251-66-3
Arbutamine hydrochloride

Guidance literature:: Multi-step reaction with 7 steps

1: 84 percent / tetrahydrofuran

2: 94 percent / H₂ / 10percent Pd-C / ethanol

3: 96 percent / NaH / dimethylformamide

4: 100 percent / LiOH / methanol; H₂O

5: 82 percent / DEPC, Et₃N / dimethylformamide / from 0 deg to RT

6: LiAlH₄ / diethyl ether / Heating

7: conc. MeOH / methanol; tetrahydrofuran / 0.5 h / Ambient temperature

With methanol; lithium hydroxide; lithium aluminium tetrahydride; hydrogen; sodium hydride; triethylamine; diethyl dicarbonate; palladium on activated charcoal; In tetrahydrofuran; methanol; diethyl ether; ethanol; water; N,N-dimethyl-formamide;
DOI:10.3987/com-97-s55