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Merck
CN

88580

Phenothiazine

purum, ≥98.0% (GC)

Synonym(s):

PTZ, 10H-Phenothiazine

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About This Item

Empirical Formula (Hill Notation):
C12H9NS
CAS Number:
92-84-2
Molecular Weight:
199.27
UNSPSC Code:
12352103
NACRES:
NA.23
PubChem Substance ID:
329769663
EC Number:
202-196-5
Beilstein/REAXYS Number:
143237
MDL number:
MFCD00005015
Assay:
≥98.0% (GC)
Technique(s):
GC/GC: suitable
Bp:
371 °C (lit.)

Key Documents

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Product Name

Phenothiazine, purum, ≥98.0% (GC)

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

purum

assay

≥98.0% (GC)

form

pellets

technique(s)

GC/GC: suitable

bp

371 °C (lit.)

mp

182-187 °C (lit.)
183-187 °C

Quality Level

200

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Related Categories

Application

Phenothiazine finds uses in metal free organic dye sensitizers, dyes and antioxidants.

General description

The structure of phenothiazine is rigid, being tricyclic. It is known to alter dopamine (3,4-dihydroxyphenethylamine). Its use as an electron donor is based on its unique hole transporting ability, electron releasing nitrogen and sulfur heteroatoms and its non-planar structure leading to lower molecular aggregation.

signalword

Warning

Hazard Classifications

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

target_organs

Blood

Storage Class

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

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Certificates of Analysis (COA)

Lot/Batch Number
WXBF5992V
WXBF3774V
WXBF1392V
WXBD6633V
WXBD5229V

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Acridine and phenothiazine derivatives as pharmacotherapeutics for prion disease
Carsten K, et al
Proceedings of the National Academy of Sciences of the USA, 98(17), 9834-9841 (2001)
A S Horn et al.
Proceedings of the National Academy of Sciences of the United States of America, 68(10), 2325-2328 (1971-10-01)
Phenothiazines and butyrophenones are known to alter dopamine (3,4-dihydroxyphenethylamine) metabolism in the brain in a fashion suggesting that they may block dopamine receptors. We observed, using Dreiding molecular models, that dopamine in its solid-state conformation is superimposable upon a portion
Photodegradation of trimeprazine triggered by self-photogenerated singlet molecular oxygen
Waseem A, et al
Journal of Saudi Chemical Society (2012)
Asif M, et al
Arabian Journal of Chemistry null
Gabriela B Rodrigues et al.
Journal of photochemistry and photobiology. B, Biology, 116, 89-94 (2012-09-18)
Photodynamic antimicrobial chemotherapy (PACT) is a promising alternative to conventional chemotherapy that can be used to treat localized mycosis. The development of PACT depends on identifying effective and selective PS for the different pathogenic species. The in vitro susceptibilities of
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