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Merck
CN

24-1560

Sigma-Aldrich

Phenothiazine

SAJ first grade

Synonym(s):

10H-Phenothiazine

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About This Item

Empirical Formula (Hill Notation):
C12H9NS
CAS Number:
92-84-2
Molecular Weight:
199.27
Beilstein:
143237
EC Number:
202-196-5
MDL number:
MFCD00005015
UNSPSC Code:
12352005
PubChem Substance ID:
329752589
Grade:
SAJ first grade
Bp:
371 °C (lit.)

Key Documents

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grade

SAJ first grade

availability

available only in Japan

dilution

(for analytical testing)

bp

371 °C (lit.)

mp

182-187 °C (lit.)

SMILES string

N1c2ccccc2Sc3ccccc13

InChI

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

InChI key

WJFKNYWRSNBZNX-UHFFFAOYSA-N

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Signal Word

Warning

Hazard Statements

H302,H317,H373,H410

Hazard Classifications

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

Target Organs

Blood

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 Information

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Certificates of Analysis (COA)

Lot/Batch Number
U2891
U2179
U4432
U2685
A9243

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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
Thankamoniamma Manju et al.
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 11(11), 1744-1755 (2012-09-04)
The reaction pathways following electronic excitation of 10-methyl phenothiazine (MPS) in the presence of oxygen have been investigated as a contribution to establish the mechanisms involved in the phototoxic reactions related to phenothiazine drugs. In the context of previously published
S C Mitchell
Current drug targets, 7(9), 1181-1189 (2006-10-05)
Phenothiazine is an aromatic tricyclic compound that first emerged from the furtive chemical activity surrounding the aniline dye industry at the latter half of the 19th century. It contains both nitrogen and sulphur atoms and is the parent molecule of
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
Suruchi Mahajan et al.
Advances in colloid and interface science, 199-200, 1-14 (2013-08-13)
Phenothiazine drugs have been the subject of great interest due to their interesting aggregation properties and ability to interact with surfactants, model lipid bilayers, and biomembranes. Since these drugs show enormous pharmacological actions and deposits on the biomembranes, their pharmacological
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