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Merck

P1260000

Phenylpropanolamine hydrochloride

European Pharmacopoeia (EP) Reference Standard

Sinónimos:

DL-Norephedrine hydrochloride, (±)-Phenylpropanolamine hydrochloride, erythro-2-Amino-1-phenyl-1-propanol hydrochloride, DL-erythro-2-Amino-1-phenyl-1-propanol hydrochloride, DL-Phenylpropanolamine hydrochloride

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About This Item

Fórmula lineal:
C6H5CH(OH)CH(NH2)CH3 · HCl
Número de CAS:
Peso molecular:
187.67
Beilstein/REAXYS Number:
3914299
MDL number:
UNSPSC Code:
12352116
PubChem Substance ID:
NACRES:
NA.24

grade

pharmaceutical primary standard

API family

propanolamine

manufacturer/tradename

EDQM

mp

194-196 °C (lit.)

application(s)

pharmaceutical (small molecule)

format

neat

storage temp.

2-8°C

SMILES string

Cl.C[C@@H](N)[C@@H](O)c1ccccc1

InChI

1S/C9H13NO.ClH/c1-7(10)9(11)8-5-3-2-4-6-8;/h2-7,9,11H,10H2,1H3;1H/t7-,9-;/m1./s1

InChI key

DYWNLSQWJMTVGJ-PRCZDLBKSA-N

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General description

This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the Authority of the issuing Pharmacopoeia.For further information and support please go to the website of the issuing Pharmacopoeia.

application

Phenylpropanolamine hydrochloride EP Reference standard, intended for use in laboratory tests only as specifically prescribed in the European Pharmacopoeia.

Biochem/physiol Actions

Mixed-acting sympathomimetic amine.

Packaging

The product is delivered as supplied by the issuing Pharmacopoeia. For the current unit quantity, please visit the EDQM reference substance catalogue.

Other Notes

Sales restrictions may apply.

related product

pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral - STOT SE 3

target_organs

Central nervous system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


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Abraham G Sarraf et al.
International journal of pharmaceutics, 481(1-2), 9-17 (2014-12-30)
The objective of this study was to tailor a drug release profile through the adjustment of some key processing parameters involved in melt-extrusion: die temperature, shear rate, die length and drug particle size. Two experimental designs were selected, namely a

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