Saltar al contenido
Merck
Todas las fotos(1)

Key Documents

View All Documentation

425346

Sigma-Aldrich

10-Methylphenothiazine

98%

Sinónimos:

10-Methyl-10H -phenothiazine, N -Methylphenothiazine

Iniciar sesiónpara Ver la Fijación de precios por contrato y de la organización
Todas las fotos(1)

About This Item

Fórmula empírica (notación de Hill):
C13H11NS
Número de CAS:
1207-72-3
Peso molecular:
213.30
EC Number:
214-896-8
MDL number:
MFCD00041836
UNSPSC Code:
12162002
PubChem Substance ID:
24866627
NACRES:
NA.23

Quality Level

100

assay

98%

mp

99-101 °C (lit.)

SMILES string

CN1c2ccccc2Sc3ccccc13

InChI

1S/C13H11NS/c1-14-10-6-2-4-8-12(10)15-13-9-5-3-7-11(13)14/h2-9H,1H3

InChI key

QXBUYALKJGBACG-UHFFFAOYSA-N

Categorías relacionadas

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Elija entre una de las versiones más recientes:

Certificados de análisis (COA)

Lot/Batch Number
0000193175
0000166541
MKBW0885V
MKBP9271V
06423DJ

¿No ve la versión correcta?

Si necesita una versión concreta, puede buscar un certificado específico por el número de lote.

Busque por un COA

¿Ya tiene este producto?

Encuentre la documentación para los productos que ha comprado recientemente en la Biblioteca de documentos.

Visite la Librería de documentos

Li Bai et al.
Yao xue xue bao = Acta pharmaceutica Sinica, 43(3), 291-294 (2008-07-17)
The electrocatalytic oxidation of glutathione (reduced form GSH) at 10-methylphenothiazine (MPT) modified carbon paste electrode (MPT/CPE) was investigated by cyclic voltammetry (CV). Although GSH itself showed a very poor electrochemical response at carbon paste electrode (CPE), the response could be
Clemens Wagner et al.
Organic & biomolecular chemistry, 6(1), 48-50 (2007-12-14)
Phenothiazine can be incorporated as a redox-active probe into DNA in two conceptually different ways: the non-nucleosidic DNA base surrogate exhibits similar properties to 10-methylphenothiazine but with no preferential base-pairing properties, whereas the phenothiazine-modified uridine has different optical and electrochemical
Henrietta Endrédi et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 63(2), 349-360 (2005-06-23)
In this work the authors deal with the vibrational spectroscopy of three derivatives of phenothiazine: the 10-methyl-10H-phenothiazine, the 10 methyl-10H-phenothiazine-3-carbaldehyde and the 10-methyl-10H-phenothiazine-3-yl-methanol. The authors investigated the vibrational spectroscopic behaviour of the phenothiazine skeleton and dealt with the aldehyde and
S A Nadeem Hashmi et al.
Organic letters, 4(26), 4571-4574 (2002-12-20)
[reaction: see text] A facile procedure for the incorporation of N-methyl phenothiazine as the terminal nucleoside in oligodeoxynucleotides is reported. The phenothiazine nucleoside analogue is synthesized and then incorporated into DNA using an automated DNA solid-phase synthesizer. Phenothiazine-labeled oligodeoxynucleotides form
G Bidan et al.
Biosensors & bioelectronics, 10(1-2), 219-229 (1995-01-01)
The electro-controlled delivery of drugs based on the doping-dedoping mechanism of Electro-Conducting Polymers is restricted to charged substances acting as dopants. In order to overcome this limitation, this study presents an approach where the trapping/delivering is based on host-guest interaction.
Ver todos los artículos relacionados

Nuestro equipo de científicos tiene experiencia en todas las áreas de investigación: Ciencias de la vida, Ciencia de los materiales, Síntesis química, Cromatografía, Analítica y muchas otras.

Póngase en contacto con el Servicio técnico