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Merck
CN

E2750

(+)-Pseudoephedrine hydrochloride

≥98%

Synonym(s):

(+)-ψ-Ephedrine hydrochloride, (1S,2S)-2-Methylamino-1-phenylpropanol hydrochloride, d-Isoephedrine hydrochloride, d-Pseudoephedrine hydrochloride

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About This Item

Linear Formula:
C6H5CH[CH(NHCH3)CH3]OH·HCl
CAS Number:
345-78-8
Molecular Weight:
201.69
UNSPSC Code:
12352210
NACRES:
NA.77
PubChem Substance ID:
24894482
EC Number:
206-462-1
Beilstein/REAXYS Number:
3915112
MDL number:
MFCD00058088

Key Documents

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InChI key

BALXUFOVQVENIU-KXNXZCPBSA-N

InChI

1S/C10H15NO.ClH/c1-8(11-2)10(12)9-6-4-3-5-7-9;/h3-8,10-12H,1-2H3;1H/t8-,10+;/m0./s1

SMILES string

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

assay

≥98%

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

mp

185-188 °C (lit.)

application(s)

forensics and toxicology
pharmaceutical (small molecule)
veterinary

Quality Level

200

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Related Categories

Biochem/physiol Actions

Non-selective adrenergic agonist; decongestant

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H302,H336

Hazard Classifications

Acute Tox. 4 Oral - STOT SE 3

target_organs

Central nervous system

Storage Class

11 - Combustible Solids

wgk

WGK 3

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
SLCL9108
SLCB3694
SLBX6334
SLBS5434
SLBR0234V

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Minjie Jiang et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 974, 126-130 (2014-12-03)
A rapid, sensitive and selective high-performance liquid chromatography-tandem mass spectrometric method (HPLC-MS) has been developed and validated for the simultaneous determination of 14-thienyl methylene matrine (TMM) and matrine (MT) in rat plasma in the present study. The analytes were separated
Minjie Jiang et al.
PloS one, 10(2), e0116010-e0116010 (2015-02-26)
A rapid, sensitive and selective high-performance liquid chromatography-tandem mass spectrometric method (HPLC-MS) was developed and validated to determine the 14-(3-methylbenzyl)matrine (3MBM) and 14-(4-methylbenzyl)matrine (4MBM) levels in rat plasma in the present study. The analytes were separated using a C18 column
Sean Ekins et al.
Drug metabolism and disposition: the biological fate of chemicals, 38(12), 2302-2308 (2010-09-17)
Drug-induced liver injury (DILI) is one of the most important reasons for drug development failure at both preapproval and postapproval stages. There has been increased interest in developing predictive in vivo, in vitro, and in silico models to identify compounds
Nigel Greene et al.
Chemical research in toxicology, 23(7), 1215-1222 (2010-06-18)
Drug-induced liver injury is a major issue of concern and has led to the withdrawal of a significant number of marketed drugs. An understanding of structure-activity relationships (SARs) of chemicals can make a significant contribution to the identification of potential
Zhichao Liu et al.
PLoS computational biology, 7(12), e1002310-e1002310 (2011-12-24)
Drug-induced liver injury (DILI) is a significant concern in drug development due to the poor concordance between preclinical and clinical findings of liver toxicity. We hypothesized that the DILI types (hepatotoxic side effects) seen in the clinic can be translated

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