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P-044

Supelco

Promethazine hydrochloride

vial of 25 mg, certified reference material, Cerilliant®

Synonyme(s) :

10-[2-(Dimethylamino)propyl]phenothiazine hydrochloride

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About This Item

Formule empirique (notation de Hill):
C17H20N2S · HCl
Numéro CAS:
58-33-3
Poids moléculaire :
320.88
Numéro Beilstein :
4166397
Numéro CE :
200-375-2
Numéro MDL:
MFCD00012652
Code UNSPSC :
41116107
ID de substance PubChem :
329820037

Qualité

certified reference material

Forme

solid

Caractéristiques

Snap-N-Spike®/Snap-N-Shoot®

Conditionnement

vial of 25 mg

Fabricant/nom de marque

Cerilliant®

Technique(s)

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

Application(s)

forensics and toxicology
pharmaceutical (small molecule)

Format

neat

Température de stockage

room temp

Chaîne SMILES 

Cl[H].CC(CN1c2ccccc2Sc3ccccc13)N(C)C

InChI

1S/C17H20N2S.ClH/c1-13(18(2)3)12-19-14-8-4-6-10-16(14)20-17-11-7-5-9-15(17)19;/h4-11,13H,12H2,1-3H3;1H

Clé InChI

XXPDBLUZJRXNNZ-UHFFFAOYSA-N

Informations sur le gène

human ... HRH1(3269)

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Description générale

Promethazine is a phenothiazine analog prescribed for treatment of motion sickness, nausea, vomiting and allergies. This Certified Reference Material is suitable for GC/MS or LC/MS methods in promethazine testing for forensic analysis, urine drug testing, or clinical toxicology. Sold under the trade names Phenergan® and Phenadoz®, promethazine has antihistamine, sedative, and mild antipsychotic effects. The compound has also been been found in the recreational drug "Purple Drank."

Informations légales

CERILLIANT is a registered trademark of Merck KGaA, Darmstadt, Germany
Phenadoz is a registered trademark of Watson Laboratories, Inc.
Phenergan is a registered trademark of Delcor Asset Corporation
Snap-N-Shoot is a registered trademark of Cerilliant Corporation
Snap-N-Spike is a registered trademark of Merck KGaA, Darmstadt, Germany

Pictogrammes

CorrosionExclamation markEnvironment
GHS05,GHS07,GHS09

Mention d'avertissement

Danger

Mentions de danger

H302,H317,H318,H411

Classification des risques

Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Dam. 1 - Skin Sens. 1

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Certificats d'analyse (COA)

Recherchez un Certificats d'analyse (COA) en saisissant le numéro de lot du produit. Les numéros de lot figurent sur l'étiquette du produit après les mots "Lot" ou "Batch".

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Consulter la Bibliothèque de documents

Gaeul Han et al.
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Postmenopausal syndrome refers to symptoms caused by the gradual decrease in female hormones after mid-40 years. As a target organ of estrogen, decrease in estrogen causes various changes in brain function such as a decrease in choline acetyltransferase and brain-derived
Elisa Izquierdo et al.
Cancer discovery (2021-11-06)
The survival of children with DIPG remains dismal, with new treatments desperately needed. In a prospective biopsy-stratified clinical trial, we combined detailed molecular profiling and drug screening in newly-established patient-derived models in vitro and in vivo. We identified in vitro
Mario Schietroma et al.
Journal of the American College of Surgeons, 220(5), 921-933 (2015-04-05)
This article has been retracted: please see Elsevier Policy on Article Withdrawal (https://www.elsevier.com/about/our-business/policies/article-withdrawal). This article has been retracted at the request of the Editor-in-Chief. An independent statistical analysis based on the summary data tables and statistical results reported in the
Shigeru Hishinuma et al.
Biochemical pharmacology, 91(2), 231-241 (2014-07-30)
Differential binding sites for first- and second-generation antihistamines were indicated on the basis of the crystal structure of human histamine H1 receptors. In this study, we evaluated differences between the thermodynamic driving forces of first- and second-generation antihistamines for human
Cheryl C Y Loh et al.
PloS one, 9(10), e110800-e110800 (2014-10-25)
Chloroquine was a cheap, extremely effective drug against Plasmodium falciparum until resistance arose. One approach to reversing resistance is the inhibition of chloroquine efflux from its site of action, the parasite digestive vacuole. Chloroquine accumulation studies have traditionally relied on
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