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Merck
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Documenti

E2750

Sigma-Aldrich

(+)-Pseudoephedrine hydrochloride

≥98%

Sinonimo/i:

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

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About This Item

Formula condensata:
C6H5CH[CH(NHCH3)CH3]OH·HCl
Numero CAS:
345-78-8
Peso molecolare:
201.69
Beilstein:
3915112
Numero CE:
206-462-1
Numero MDL:
MFCD00058088
Codice UNSPSC:
12352210
ID PubChem:
24894482
NACRES:
NA.77

Saggio

≥98%

tecniche

HPLC: suitable
gas chromatography (GC): suitable

Punto di fusione

185-188 °C (lit.)

applicazioni

forensics and toxicology
pharmaceutical (small molecule)
veterinary

Stringa SMILE

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
BALXUFOVQVENIU-KXNXZCPBSA-N

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Azioni biochim/fisiol

Non-selective adrenergic agonist; decongestant

Pittogrammi

Exclamation mark
GHS07

Avvertenze

Warning

Indicazioni di pericolo

H302,H336

Classi di pericolo

Acute Tox. 4 Oral - STOT SE 3

Organi bersaglio

Central nervous system

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Dispositivi di protezione individuale

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

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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
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
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

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