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46624

Supelco

Phénothiazine

VETRANAL®, analytical standard

Synonyme(s) :

10H-Phénothiazine

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About This Item

Formule empirique (notation de Hill):
C12H9NS
Numéro CAS:
92-84-2
Poids moléculaire :
199.27
Numéro Beilstein :
143237
Numéro CE :
202-196-5
Numéro MDL:
MFCD00005015
Code UNSPSC :
41116107
ID de substance PubChem :
329757221
Nomenclature NACRES :
NA.24

Qualité

analytical standard

Niveau de qualité

200

Gamme de produits

VETRANAL®

Pureté

≥98%

Forme

powder

Durée de conservation

limited shelf life, expiry date on the label

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Point d'ébullition

371 °C (lit.)

Pf

182-187 °C (lit.)

Application(s)

cleaning products
clinical
cosmetics
food and beverages
forensics and toxicology
personal care
pharmaceutical (small molecule)

Format

neat

Chaîne SMILES 

N1c2ccccc2Sc3ccccc13

InChI

1S/C12H9NS/c1-3-7-11-9(5-1)13-10-6-2-4-8-12(10)14-11/h1-8,13H

Clé InChI

WJFKNYWRSNBZNX-UHFFFAOYSA-N

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Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Produits recommandés

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.

Informations légales

VETRANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

Produit(s) apparenté(s)

Réf. du produit
Description
Tarif

903167

10-Phenylphenothiazine, ≥95%

Pictogrammes

Health hazardExclamation markEnvironment
GHS08,GHS07,GHS09

Mention d'avertissement

Warning

Mentions de danger

H302,H317,H373,H410

Classification des risques

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Skin Sens. 1 - STOT RE 2 Oral

Organes cibles

Blood

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

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

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Certificats d'analyse (COA)

Lot/Batch Number
BCCG4664
BCBT8605
SZBC249XV
SZB7318XV
SZE7318X

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Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

V P Volkov
Klinicheskaia meditsina, 89(4), 27-30 (2011-09-22)
Ten most common and clinically significant pathological changes of ECG in schizophrenic patients with and without phenothiazine-induced cardiomyopathy (PCMP) at different stages of neuroleptic therapy are considered. A total of 46 men and 10 women were available for observation. The
Sh Y Mamedov et al.
Bulletin of experimental biology and medicine, 150(5), 576-578 (2012-01-12)
We studied the effects of natural (α-tocopherol and SOD) and synthetic (potassium phenosane and hydroxypyridine) antioxidants on the recovery of disordered parameters of the electroretinogram under conditions of high-intensity light exposure. Potassium phenosane and tocopherol acetate more effectively normalized parameters
Caiwen Ou et al.
Chemical communications (Cambridge, England), 49(18), 1853-1855 (2013-01-31)
We report a 'super-gelator' of a short peptide capped with phenothiazine acetic acid.
Daniella Takács et al.
Bioorganic & medicinal chemistry, 20(14), 4258-4270 (2012-06-29)
N-dienylphenothiazines synthesized from tetrazolo[1,5-a]pyridinium salts by treatment with phenothiazine were subjected to catalytic hydrogenation to yield N-butylphenothiazines, whereas transformation of these dienes with borane dimethyl sulfide (BH(3) × Me(2)S) resulted in selective hydroboration of one double bond and full reduction
Alina N Sekretaryova et al.
Analytical chemistry, 84(3), 1220-1223 (2011-12-31)
Wiring glucose oxidase in the membrane with an immobilized mediator is possible due to the diffusion ability of the latter, if the enzyme containing membrane is formed according to the proposed protocol, including exposing proteins to water-organic mixtures with the
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