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Safety Information

425346

Sigma-Aldrich

10-Methylphenothiazine

98%

Synonym(s):

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

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About This Item

Empirical Formula (Hill Notation):
C13H11NS
CAS Number:
1207-72-3
Molecular Weight:
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

Related Categories

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

425346-BULK:
425346-5G:
425346-VAR:
425346-25G:

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Certificates of Analysis (COA)

Lot/Batch Number
MKBW0885V
MKBP9271V
06423DJ
11024CD
07315TG

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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
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.
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
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
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