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P-038

Supelco

(±)-Phenylpropanolamine hydrochloride solution

1.0 mg/mL in methanol (as free base), ampule of 1 mL, certified reference material, Cerilliant®

Synonym(s):

DL-Norephedrine hydrochloride, 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

Linear Formula:
C6H5CH(OH)CH(NH2)CH3 · HCl
CAS Number:
154-41-6
Molecular Weight:
187.67
Beilstein/REAXYS Number:
3914299
EC Number:
200-659-6
MDL number:
MFCD00013019
UNSPSC Code:
41116107
PubChem Substance ID:
329820034
NACRES:
NA.24

grade

certified reference material

Quality Level

300

form

liquid

feature

Snap-N-Spike®/Snap-N-Shoot®

packaging

ampule of 1 mL

manufacturer/tradename

Cerilliant®

concentration

1.0 mg/mL in methanol (as free base)

technique(s)

gas chromatography (GC): suitable
liquid chromatography (LC): suitable

mp

194-196 °C (lit.)

application(s)

clinical testing

format

single component solution

storage temp.

−20°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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Related Categories

General description

Phenylpropanolamine, also known as Norephedrine, is a stimulant, decongestant, and anorectic drug commonly used in many prescription and over-the-counter cold and cough formulations. The drug is often abused illicitly for its psychoactive and stimulant effects. This Certified Spiking Solution® is applicable for use in many LC-MS/MS or GC/MS applications from clinical chemistry and forensic analysis to urine drug testing.

Application

  • The effects of drug-drug interaction on linezolid pharmacokinetics: A systematic review: This review assesses the interaction of various drugs with linezolid, where (±)-Phenylpropanolamine hydrochloride serves as a reference compound. It provides valuable data on the stability and interaction of pharmaceutical intermediates, highlighting the importance of (±)-Phenylpropanolamine hydrochloride in developing safer drug therapies (Xu et al., 2024).

Biochem/physiol Actions

Mixed-acting sympathomimetic amine.

Recommended products

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Legal Information

CERILLIANT is a registered trademark of Merck KGaA, Darmstadt, Germany
CERTIFIED SPIKING SOLUTION is a registered trademark of Cerilliant Corporation
Snap-N-Shoot is a registered trademark of Cerilliant Corporation
Snap-N-Spike is a registered trademark of Merck KGaA, Darmstadt, Germany

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signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Flam. Liq. 2 - STOT SE 1

wgk_germany

WGK 1

flash_point_f

closed cup

flash_point_c

closed cup

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Sigma-Aldrich

C222

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DL-Norephedrine hydrochloride ≥99%

Sigma-Aldrich

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S(+)-Methamphetamine solution

(±)-Amphetamine solution 1.0 mg/mL in methanol, ampule of 1 mL, certified reference material, Cerilliant®

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A-007

(±)-Amphetamine solution

DL-Ephedrine hydrochloride 99%

Sigma-Aldrich

285749

DL-Ephedrine hydrochloride

A Pokrywka et al.
International journal of sports medicine, 30(8), 569-572 (2009-04-22)
Pseudoephedrine (PSE) as a sympathomimetic is an ingredient of many proprietary medicines which are available on the medical market over the counter (OTC drugs). It can be converted to cathine (CATH, norpseudoephedrine) inside the body. Until the end of 2003
Richard Hoffman et al.
Journal of ethnopharmacology, 132(3), 554-563 (2010-06-18)
Although there is a rich body of research available regarding the effect of acute and chronic khat dosing in animal models, research on the behavioral and cognitive effects of khat in human subjects is not extensive and several of the
Saba Kassim et al.
Journal of ethnopharmacology, 140(1), 193-196 (2012-01-17)
Khat chewing amongst the UK communities originating from Yemen and the East African coast is suggested to create dependency through its main stimulant components (cathinone, norephedrine and norpseudoephedrine) on the central nervous system. To validate self-reported khat chewing behaviours by
Keep an eye on the pupil: developing countries under chemical attack.
Husni Al-Goshae et al.
Internal and emergency medicine, 4(3), 231-233 (2009-04-16)
K Deventer et al.
Drug testing and analysis, 1(5), 209-213 (2010-04-01)
Until the end of 2003 a urinary concentration of pseudoephedrine exceeding 25 microg/mL was regarded as a doping violation by the World Anti-Doping Agency. Since its removal from the prohibited list in 2004 the number of urine samples in which
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