46624
吩噻嗪
VETRANAL®, analytical standard
别名:
10H-吩噻嗪
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关于此项目
经验公式（希尔记法）:
C12H9NS
化学文摘社编号:
分子量:
199.27
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
202-196-5
Beilstein/REAXYS Number:
143237
MDL number:
InChI key
WJFKNYWRSNBZNX-UHFFFAOYSA-N
InChI
1S/C12H9NS/c1-3-7-11-9(5-1)13-10-6-2-4-8-12(10)14-11/h1-8,13H
SMILES string
N1c2ccccc2Sc3ccccc13
grade
analytical standard
product line
VETRANAL®
assay
≥98%
form
powder
shelf life
limited shelf life, expiry date on the label
technique(s)
HPLC: suitable, gas chromatography (GC): suitable
bp
371 °C (lit.)
mp
182-187 °C (lit.)
application(s)
cleaning products
clinical
cosmetics
food and beverages
forensics and toxicology
personal care
pharmaceutical (small molecule)
format
neat
Quality Level
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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.
Other Notes
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.
Legal Information
VETRANAL is a registered trademark of Merck KGaA, Darmstadt, Germany
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Skin Sens. 1 - STOT RE 2 Oral
target_organs
Blood
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
Tatsuya Hoshino et al.
Bioelectrochemistry (Amsterdam, Netherlands), 84, 1-5 (2011-10-07)
We report on a novel fabrication approach of amperometric biosensor based on multilayer films containing carbon nanotubes (CNT), a nano-thin plasma-polymerized film (PPF), electron transfer mediator phenothiazine (PT), and enzyme glucose dehydrogenase (GDH). The configuration of the electrochemical electrode is
Aaron S Hart et al.
ACS applied materials & interfaces, 4(11), 5813-5820 (2012-10-10)
Effect of positioning of the cyanoacrylic acid anchoring group on ring periphery of phenothiazine dye on the performance of dye-sensitized solar cells (DSSCs) is reported. Two types of dyes, one having substitution on the C-3 aromatic ring (Type 1) and
P Halaburda et al.
Talanta, 96, 202-209 (2012-07-24)
A rapid, sensitive and fully automated chemiluminometric method is described for determination of five phenothiazine derivatives, namely, trifluoperazine, fluphenazine, perphenazine, thioridazine and chlorpromazine. The method is based on the chemiluminescence (CL) induced by the oxidation of drugs with Ce(IV) in
Investigation of the influence of phenosan, ichphan-10, and melafen on red blood cells in vivo by atomic force microscopy.
V I Binyukov et al.
Doklady. Biochemistry and biophysics, 441, 245-247 (2012-01-06)
Mechanistic basis of phenothiazine-driven inhibition of Tau aggregation.
Elias Akoury et al.
Angewandte Chemie (International ed. in English), 52(12), 3511-3515 (2013-02-13)
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