mesoridazine
- Product Name
- mesoridazine
- CAS No.
- 5588-33-0
- Chemical Name
- mesoridazine
- Synonyms
- TPS 23;NSC 186066;MESORIDAZINE;Mesoridazine free base;Thioridazine-2-sulfoxide;Thioridazine EP Impurity B;mesoridazine ISO 9001：2015 REACH;Thioridazine EP Impurity B-d3 (Mesoridazine-d3);10-[2-(1-methyl-2-piperidyl)ethyl]-2-methylsulfinyl-phenothiazine;10-[2-(1-methylpiperidin-2-yl)ethyl]-2-methylsulfinylphenothiazine
- CBNumber
- CB0875422
- Molecular Formula
- C21H26N2OS2
- Formula Weight
- 386.57
- MOL File
- 5588-33-0.mol
mesoridazine Property
- Melting point:
- 128-131 °C
- Boiling point:
- 570.5±50.0 °C(Predicted)
- Density
- 1.1234 (rough estimate)
- refractive index
- 1.5950 (estimate)
- solubility
- Acetonitrile: slightly soluble; DMSO: slightly, heated; Methanol: slightly soluble
- form
- Sticky Solid
- pka
- 9.84±0.10(Predicted)
- color
- Pale Yellow to Orange
- Stability:
- Hygroscopic
Safety
- Hazardous Substances Data
- 5588-33-0(Hazardous Substances Data)
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Danger
- Hazard statements
-
H225Highly Flammable liquid and vapour
H319Causes serious eye irritation
- Precautionary statements
-
P210Keep away from heat/sparks/open flames/hot surfaces. — No smoking.
P233Keep container tightly closed.
P240Ground/bond container and receiving equipment.
P241Use explosion-proof electrical/ventilating/lighting/…/equipment.
P242Use only non-sparking tools.
P243Take precautionary measures against static discharge.
P261Avoid breathing dust/fume/gas/mist/vapours/spray.
P264Wash hands thoroughly after handling.
P264Wash skin thouroughly after handling.
P270Do not eat, drink or smoke when using this product.
P271Use only outdoors or in a well-ventilated area.
P280Wear protective gloves/protective clothing/eye protection/face protection.
P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.
P303+P361+P353IF ON SKIN (or hair): Remove/Take off Immediately all contaminated clothing. Rinse SKIN with water/shower.
P304+P340IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
P321Specific treatment (see … on this label).
P330Rinse mouth.
P337+P313IF eye irritation persists: Get medical advice/attention.
P370+P378In case of fire: Use … for extinction.
P403+P235Store in a well-ventilated place. Keep cool.
P501Dispose of contents/container to..…
N-Bromosuccinimide Price
- Product number
- M225760
- Product name
- Mesoridazine
- Packaging
- 5mg
- Price
- $65
- Updated
- 2021/12/16
- Product number
- 0470CA
- Product name
- Mesoridazine
- Packaging
- 10mg
- Price
- $139
- Updated
- 2021/12/16
- Product number
- 0470CA
- Product name
- Mesoridazine
- Packaging
- 50mg
- Price
- $266
- Updated
- 2021/12/16
- Product number
- API0009156
- Product name
- MESORIDAZINE
- Purity
- 95.00%
- Packaging
- 10MG
- Price
- $750.75
- Updated
- 2021/12/16
- Product number
- API0009156
- Product name
- MESORIDAZINE
- Purity
- 95.00%
- Packaging
- 100MG
- Price
- $1963.5
- Updated
- 2021/12/16
mesoridazine Chemical Properties,Usage,Production
Chemical Properties
Pale Pink Solid
Originator
Serentil,Sandoz,US,1970
Uses
Mesoridazine (Thioridazine EP Impurity B) is an antipsychotic.
Uses
Mesoridazine is an antipsychotic.
Definition
ChEBI: A phenothiazine substituted at position 2 (para to the S atom) by a methylsulfinyl group, and on the nitrogen by a 2-(1-methylpiperidin-2-yl)ethyl group.
Manufacturing Process
10.0 g of 3-methylmercapto phenothiazine and 17.5 cc of acetic acid
anhydride are refluxed for 8 hours from an oil bath maintained at a
temperature of 180°C. After concentration of the solution the residue is
crystallized from ethanol. The pure 3-methylmercapto-10-acetyl phenothiazine
melts at 89° to 91°C. For the purpose of oxidation 5.0 g of 3-
methylmercapto-10-acetyl phenothiazine are dissolved in 50 cc of ethanol,
refluxed from an oil bath maintained at 120°C and 1.6 cc of a 40% hydrogen
peroxide solution are then added dropwise in the course of 30 minutes.
Heating is continued for another 5 hours and the reaction mixture is
concentrated after 50 cc of water have been added. The residue is taken up in
40 cc of benzene and the benzene layer washed with 10 cc of water. After
having been concentrated, the residue, crude 3-methylsulfinyl-10-acetyl
phenothiazine, is dissolved in 55 cc of a 90% methanol solution for splitting
off the acetyl group and, after 2.9 g of potassium carbonate have been added,
it is boiled for 2 hours under reflux on an oil bath kept at a temperature of
120°C. After concentration, the residue is taken up in 50 cc of chloroform, the
chloroform layer is washed with a total of 25 cc of water, dried over potassium
carbonate, filtered and concentrated. After twice crystallizing the residue, each
time from 50 cc of ethanol, analytically pure 3-methylsulfinyl phenothiazine
(MP 193° to 195°C) is obtained.
A mixture of 10.0 g of 3-methylsulfinyl phenothiazine (MP 193° to 195°C), 6.1
g of finely powdered sodium hydroxide and 125 cc of toluene is boiled for 1
hour under reflux with a water separator on an oil bath kept at a temperature
of 150°C, while the mixture is stirred. Without interrupting the boil a solution
of 7.0 g of 2-(N-methyl-piperidyl-2')-1-chloroethane (BP 84°C/10 mm Hg) in
10 cc of toluene is added dropwise in the course of 1 hour, after which boiling
is continued for another 3 hours. When the reaction mixture has cooled it is
first washed with 25 cc of water three times and then extracted with 75 cc of
a 15% aqueous tartaric acid solution. The tartaric acid extract is shaken out
with 25 cc of benzene, 20 cc of concentrated caustic soda are added until the
phenolphthalein reaction is alkaline, and the separated oily base is taken up in
a total of 150 cc of benzene.
After having been washed with 50 cc of water the benzene layer is dried over
potassium carbonate, filtered, allowed to stand over 10 g of alumina for about
1? hours for partial decolorization, filtered again and concentrated under
reduced pressure. The oily base which remains as a residue is directly
converted into the tartrate. A solution cooled to 0°C, of 6.50 g of the free
base in 100 cc of acetic acid ethyl ester is thoroughly shaken and poured into
an ice cold solution of 2.66 g of tartaric acid in 410 cc of acetic acid ethyl
ester. The precipitated, analytically pure, tartrate of 3-methylsulfinyl-10-[2'-Nmethyl-piperidyl-2')-ethyl-l']-phenothiazine melts at 115° to 120°C (foam
formation) and sinters above 80°C. The base is reacted with benzene sulfonic
acid in a suitable solvent to give the besylate.
brand name
Serentil (Novartis).
Therapeutic Function
Tranquilizer
mesoridazine Preparation Products And Raw materials
Raw materials
Preparation Products
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