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prednimustine

CAS No.
29069-24-7
Chemical Name:
prednimustine
Synonyms
LEO-1031;Sterecyt;Stereocyt;NSC 171345;NSC-134087;Prednimustin;prednimustine;prednimustine USP/EP/BP;HFVNWDWLWUCIHC-GUPDPFMOSA-N;Prednisolone chloraMbucil ester
CBNumber:
CB7933444
Molecular Formula:
C35H45Cl2NO6
Molecular Weight:
646.64
MDL Number:
MFCD00866487
MOL File:
29069-24-7.mol
Last updated:2023-05-04 17:34:37

prednimustine Properties

Melting point 163-164°
alpha D24 +92.9° (c = 1.06 in chloroform)
Boiling point 791.5±60.0 °C(Predicted)
Density 1.30±0.1 g/cm3(Predicted)
pka 12.32±0.70(Predicted)
FDA UNII 9403SIO2S8
IARC 3 (Vol. 50) 1990
ATC code L01AA08

prednimustine price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
American Custom Chemicals Corporation API0012322 PREDNIMUSTINE 95.00% 29069-24-7 5MG $495.74 2021-12-16 Buy
Product number Packaging Price Buy
API0012322 5MG $495.74 Buy

prednimustine Chemical Properties,Uses,Production

Originator

Stereocyt, Bellon ,France ,1978

Uses

Antineoplastic.

Definition

ChEBI: Prednimustine is a corticosteroid hormone.

Manufacturing Process

p-[N-bis(β-chloroethyl)amino] phenyl butyric acid was dissolved in a mixture of 150 ml dry benzene and 8.04 ml dry pyridine. The solution was cooled in an ice bath, and a solution of thionyl chloride in 30 ml dry benzene was slowly added with stirring under anhydrous conditions.
The reaction mixture was then kept at room temperature for 1 hour and thereafter poured into a mixture of 5.0 N HCl and crushed ice. The benzene solution was immediately washed with water, with cold 1.0 N NaHCO3 and finally with cold water. After drying over anhydrous sodium sulfate, the benzene was removed in vacuo. The residue is the p-[N-bis(βchloroethyl)amino]phenyl butyric anhydride which could be used without any further purification.
To a solution of 42.0 g of p-[N-bis(β-chloroethyl)amino]phenyl butyric anhydride in 500 ml dry pyridine was added 24.4 g of prednisolone. The reaction mixture was kept at room temperature for 24 hours under anhydrous condition. It was then poured into a mixture of concentrated HCl and crushed ice and extracted with ether-ethyl acetate (1:1).
The organic phase was washed several times with cold 1.0 N K2CO3 and finallywater. After drying over CaCl2 the solvent was removed in vacuo.
The residue is prednisolone 21-[4'-[p-bis(β-chloroethyl)amino]phenyl]butyrate which after crystallization from methanol/water had a melting point of 163°C to 164°C.

Therapeutic Function

Cancer chemotherapy

prednimustine Preparation Products And Raw materials

Raw materials

Preparation Products

prednimustine Suppliers

Global( 8)Suppliers
Supplier Tel Email Country ProdList Advantage
Dideu Industries Group Limited
+86-29-89586680 +86-15129568250 1026@dideu.com China 29220 58
LGM Pharma 1-(800)-881-8210 inquiries@lgmpharma.com United States 2127 70
Shaanxi Dideu Newmaterial Co., Ltd. 029-63373950 15353716720 1052@dideu.com China 10007 58

View Lastest Price from prednimustine manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
prednimustine USP/EP/BP pictures 2021-07-06 prednimustine USP/EP/BP
29069-24-7
US $1.10 / g 1g 99.9% 100 Tons Min Dideu Industries Group Limited
prednimustine Prednimustin 21-[4-[p-[Bis(2-chloroethyl)amino]phenyl]-1-oxobutoxy]-11β,17-dihydroxypregna-1,4-diene-3,20-dione Chlorambucil prednisolone ester LEO-1031 NSC-134087 Stereocyt NSC 171345 Prednisolone chloraMbucil ester Sterecyt HFVNWDWLWUCIHC-GUPDPFMOSA-N Pregna-1,4-diene-3,20-dione, 21-[4-[4-[bis(2-chloroethyl)amino]phenyl]-1-oxobutoxy]-11,17-dihydroxy-, (11β)- prednimustine USP/EP/BP 29069-24-7 C35H45Cl2NO6