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metopimazine

CAS No.
14008-44-7
Chemical Name:
metopimazine
Synonyms
NG101;NG 101;NG-101;RP-9965;EXP 999;9965 RP;Nortrip;Vogalene;metopimazine;metopimazine USP/EP/BP
CBNumber:
CB0934482
Molecular Formula:
C22H27N3O3S2
Molecular Weight:
445.59808
MDL Number:
MFCD00837528
MOL File:
14008-44-7.mol
MSDS File:
SDS
Last updated:2023-05-04 17:34:33

metopimazine Properties

Melting point 170.5℃
Boiling point 721.2±60.0 °C(Predicted)
Density 1.1920 (rough estimate)
refractive index 1.6320 (estimate)
storage temp. Refrigerator
solubility DMSO (Slightly), Methanol (Slightly)
form Solid
pka 16.44±0.20(Predicted)
color Pale Yellow
CAS DataBase Reference 14008-44-7
FDA UNII 238S75V9AV
ATC code A04AD05

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302
Precautionary statements  P264-P270-P301+P312-P330-P501
Toxicity LD50 in male rats (mg/kg): 976 orally, 1080 s.c. (Goldenthal)

metopimazine price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TRC M338760 Metopimazine 14008-44-7 50mg $1695 2021-12-16 Buy
American Custom Chemicals Corporation API0008052 METOPIMAZINE 95.00% 14008-44-7 50MG $1871.1 2021-12-16 Buy
American Custom Chemicals Corporation API0008052 METOPIMAZINE 95.00% 14008-44-7 5MG $385 2021-12-16 Buy
Product number Packaging Price Buy
M338760 50mg $1695 Buy
API0008052 50MG $1871.1 Buy
API0008052 5MG $385 Buy

metopimazine Chemical Properties,Uses,Production

Chemical Properties

Pale Yellow Solid

Originator

Nortrip,Rhodia

Uses

metopimazine is used to prevent emesis during chemotherapies.

Uses

Metopimazine (MPZ) is used to prevent emesis during chemotherapies. Antiemetic.

Definition

ChEBI: Metopimazine is a member of phenothiazines.

Manufacturing Process

2-Methylsulfonyl-10-(3-chloropropyl)phenothiazine was prepared by condensation of 1-bromo-3-chloropropane and 2-methylsulfonyl phenothiazine in liquid ammonia in presence of obtained in situ sodium amide.
10 g 2-methylsulfonyl-10-(3-chloropropyl)-phenothiazine, 4 g piperidine-4- carboxylic acid amide, 3.5 g dry sodium carbonate in 200 ml of ethanol was heated to reflux for 24 hours. Than 1.75 g sodium carbonate was added and the mixture was heated another 8 hours. After that the new 1.75 g portion of sodium carbonate was added and heated for 16 hours. The solvent was removed in vacuum (20 mm Hg). The residue was stirred with 50 ml water and 150 ml ethyl acetate. The organic layer was separated and extracted with 200 ml 1 N hydrochloric acid. The water layer was made alkaline with 4 N sodium hydroxide, extracted with ethyl acetate and dried over sodium sulfate. The solvent was removed in vacuum (20 mm Hg) to dryness. The obtained residue 2-methylsulfonyl-10-(3-(4-carbamoylpiperidino)propyl)phenothiazine was recrystallized from ethyl acetate. Yield 6 g; MP: 170°-171°C.

Therapeutic Function

Antiemetic

metopimazine Preparation Products And Raw materials

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+86-852-30606658 market18@leapchem.com China 43348 58
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metopimazine 1-[3-[2-[Methylsulfonyl] phenothiazin-10-yl] propyl] isonipecotamide 1-[3-(2-Methylsulfonyl-10H-phenothiazin-10-yl)propyl]-4-piperidinecarboxamide 9965 RP EXP 999 RP-9965 Vogalene 1-[3-[2-(Methylsulfonyl)-10H-phenothiazin-10-yl]propyl]piperidin-4-carboxaMide 2-Methylsulfonyl-10-[3-(4-carbamoylpiperidino)propyl]phenothiazine 4-PiperidinecarboxaMide,1-[3-[2-(Methylsulfonyl)-10H-phenothiazin-10-yl]propyl]- 1-(3-(2-(methylsulfonyl)-10H-phenothiazin-10-yl)propyl)piperidine-4-carboxamide 1-[3-(2-Methylsulfonylphenothiazin-10-yl)propyl]piperidine-4-carboxaMide metopimazine USP/EP/BP NG 101 NG101 NG-101 Nortrip 14008-44-7 C22H21D6N3O3S2 Amines Aromatics Heterocycles Intermediates & Fine Chemicals Pharmaceuticals Sulfur & Selenium Compounds Isotope Labelled Compounds