trimetozine
- Product Name
- trimetozine
- CAS No.
- 635-41-6
- Chemical Name
- trimetozine
- Synonyms
- V 7;Opalene;PS-2383;PS 2383;NSC-62939;Trioxazin;Sedoxazine;TriMetozin;Trioxazine;Abbott-22370
- CBNumber
- CB5875528
- Molecular Formula
- C14H19NO5
- Formula Weight
- 281.3
- MOL File
- 635-41-6.mol
trimetozine Property
- Melting point:
- 120-122°
- Boiling point:
- 423.97°C (rough estimate)
- Density
- 1.1755 (rough estimate)
- refractive index
- 1.5230 (estimate)
- pka
- -1.60±0.20(Predicted)
- form
- Solid
- color
- White to off-white
Safety
- Toxicity
- LD50 oral in rat: 1800mg/kg
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H302Harmful if swallowed
- Precautionary statements
-
P264Wash hands thoroughly after handling.
P264Wash skin thouroughly after handling.
P270Do not eat, drink or smoke when using this product.
P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.
P330Rinse mouth.
P501Dispose of contents/container to..…
N-Bromosuccinimide Price
- Product number
- S570621
- Product name
- 4-(3,4,5-TRIMETHOXYBENZOYL)-MORPHOLINE
- Purity
- AldrichCPR
- Packaging
- 250MG
- Price
- $179
- Updated
- 2024/03/01
- Product number
- T798200
- Product name
- Trimetozine
- Packaging
- 5g
- Price
- $1055
- Updated
- 2021/12/16
- Product number
- 62447
- Product name
- Trimetozine
- Packaging
- 5G
- Price
- $1460
- Updated
- 2021/12/16
trimetozine Chemical Properties,Usage,Production
Originator
Opalene,Theraplix,France,1966
Uses
antiurolithic, depigmentation, radiation protectant
Uses
A sedative with mild tranquilizing effects. It has been used therapeutically in the treatment of anxiety. It is also a metabolite of the antisecretory and antiulcer drug Trithiozine.
Uses
A sedative with mild tranquilizing effects. Trimetozine has been used therapeutically in the treatment of anxiety. It is also a metabolite of the antisecretory and antiulcer drug Trithiozine.
Definition
ChEBI: 4-morpholinyl-(3,4,5-trimethoxyphenyl)methanone is a member of morpholines.
Manufacturing Process
46 g 3,4,5-trimethoxybenzoyl chloride are dissolved in 300 ml anhydrous benzene and 25 g triethylamine and thereafter 19 g anhydrous morpholine are added in small portions with ice-cooling. The solution is boiled for 2 hours under reflux. The precipitate is filtered off, and the solution is washed with dilute sulfuric acid, then with sodium hydrogen carbonate solution and finally with water, and then evaporated. The residual yellow oil soon crystallizes; the crystalline mass of the desired material is taken up with ether, filtered and then recrystallized from 90% ethanol, from which it separates in prisms. It is slightly soluble in water. Yield: 80%. melting point 120°C to 122°C.
Therapeutic Function
Sedative
trimetozine Preparation Products And Raw materials
Raw materials
Preparation Products
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