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E2750

Sigma-Aldrich

(+)-Pseudoephedrin -hydrochlorid

≥98%

Synonym(e):

(+)-ψ-Ephedrin -hydrochlorid, (1S,2S)-2-Methylamino-1-phenylpropanol -hydrochlorid, d-Isoephedrin -hydrochlorid, d-Pseudoephedrin -hydrochlorid

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About This Item

Lineare Formel:
C6H5CH[CH(NHCH3)CH3]OH·HCl
CAS-Nummer:
345-78-8
Molekulargewicht:
201.69
Beilstein:
3915112
EG-Nummer:
206-462-1
MDL-Nummer:
MFCD00058088
UNSPSC-Code:
12352210
PubChem Substanz-ID:
24894482
NACRES:
NA.77

Assay

≥98%

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

mp (Schmelzpunkt)

185-188 °C (lit.)

Anwendung(en)

forensics and toxicology
pharmaceutical (small molecule)
veterinary

SMILES String

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

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

InChIKey

BALXUFOVQVENIU-KXNXZCPBSA-N

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Verwandte Kategorien

Biochem./physiol. Wirkung

Nicht-selektiver adrenergischer Agonist; abschwellend

Piktogramme

Exclamation mark
GHS07

Signalwort

Warning

H-Sätze

H302,H336

Gefahreneinstufungen

Acute Tox. 4 Oral - STOT SE 3

Zielorgane

Central nervous system

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Persönliche Schutzausrüstung

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

Analysenzertifikate (COA)

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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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