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ARANIDIPINE

CAS No.
86780-90-7
Chemical Name:
ARANIDIPINE
Synonyms
Sapresta;MPC-1304;ARANIDIPINE;Asanidipine;Aranidipine MPC1304;ARANIDIPINE USP/EP/BP;ARANIDIPINE MPC1304;MPC-1304;MPC 1304;Calcium Channel,inhibit,MPC 1304,Inhibitor,MPC-1304,Aranidipine,Ca channels,Ca2+ channels;3-Methyl 5-(2-oxopropyl) 2,6-diMethyl-4-(2-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate;2,6-Dimethyl-4-(2-nitrophenyl)-1,4-dihydro-3,5-pyridinedicarboxylic acid methyl 2-oxopropyl ester
CBNumber:
CB4386708
Molecular Formula:
C19H20N2O7
Molecular Weight:
388.37
MDL Number:
MFCD00865813
MOL File:
86780-90-7.mol
Last updated:2023-05-18 11:31:13

ARANIDIPINE Properties

Melting point 155°
Boiling point 530.0±50.0 °C(Predicted)
Density 1.284±0.06 g/cm3(Predicted)
storage temp. 2-8°C
solubility DMSO : 125 mg/mL (321.86 mM)
pka 2.56±0.70(Predicted)
FDA UNII 4Y7UR6X2PO

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302+H312+H332
Precautionary statements  P261-P264-P270-P271-P280-P301+P312+P330-P302+P352+P312+P362+P364-P304+P340+P312-P501
Toxicity LD50 in male, female mice, rats (mg/kg): 143, 193, 1982, 1459 orally; LD50 in male, female mice (mg/kg): 7.3, 9.1 i.p. (Nakano)

ARANIDIPINE price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
ChemScene CS-7341 Aranidipine 99.33% 86780-90-7 5mg $60 2021-12-16 Buy
ChemScene CS-7341 Aranidipine 99.33% 86780-90-7 10mg $105 2021-12-16 Buy
ChemScene CS-7341 Aranidipine 99.33% 86780-90-7 50mg $315 2021-12-16 Buy
ChemScene CS-7341 Aranidipine 99.33% 86780-90-7 100mg $535 2021-12-16 Buy
Biorbyt Ltd orb573449 Aranidipine (MPC1304) >98% 86780-90-7 100mg $986 2021-12-16 Buy
Product number Packaging Price Buy
CS-7341 5mg $60 Buy
CS-7341 10mg $105 Buy
CS-7341 50mg $315 Buy
CS-7341 100mg $535 Buy
orb573449 100mg $986 Buy

ARANIDIPINE Chemical Properties,Uses,Production

Description

Aranidipine was launched in Japan as an antihypertensive agent. Its pharmacological effects are similar to other dihydropyridine derivatives, e.g., nefidipine, however, it is more potent and longer lasting. This is partially due to the fact that its initial metabolite (ketone reduction) is just as effective as the parent compound. Aranidipine exerts its activity by blocking Ca+2 entry during depolarization via L-type voltagegated Ca channels. This causes decreased levels of intracellular Ca which leads to enhanced relaxation of smooth and cardiac muscle. It is a selective α2-adrenoreceptor antagonist which inhibits vasoconstrictive responses. As a dihydropyridine derivative, it can be synthesized via a modified Hantsch synthesis. While sold as a racemate, the (S)-enantiomer is 150 times more active than the (R)- antipode.

Originator

Maruko Seiyaku (Japan)

Definition

ChEBI: Aranidipine is an organic molecular entity.

Manufacturing Process

100.0 mg of 50% sodium hydride was added to a mixture of 20.0 g of 2,2- ethylenedioxypropanol and 100 ml of benzene, and 20.0 g of diketene was added dropwise to the mixture while refluxing the mixture. After refluxing the mixture for 2 h, the solvent was distilled off and the resulting residue was distilled under reduced pressure to obtain 21.5 g (70% yield) of 2,2- ethylenedioxypropyl acetoacetate as a colorless oil, boiling point of 90°C (6 mm Hg).
Ammonia gas was passed through a mixture of 19.0 g of 2,2- ethylenedioxypropyl acetoacetate and 100 ml of methanol for 2.5 h under icecooling while stirring. The solvent was then distilled off and the residue was distilled under reduced pressure to obtain 16.0 g (84% yield) of 2,2- ethylenedioxypropyl 3-aminocrotonate as a pale yellow oil, boiling point of 120°C (5 mm Hg).
A mixture of methyl 2'-nitrobenzylidene acetoacetate, 2,2-ethylenedioxypropyl 3-aminocrotonate and ethanol was refluxed for 10 h. The resulting reaction solution was allowed to stand overnight, and the precipitated crystals were collected by filtration and recrystallized from ethanol to obtain methyl 2,2- ethylenedioxypropyl 2,6-dimethyl-4-(2-nitrophenyl)-1,4-dihydropyridine-3,5- dicarboxylate.
Methyl 2,2-ethylenedioxypropyl 2,6-dimethyl-4-(2-nitrophenyl)-1,4- dihydropyridine-3,5-dicarboxylate was refluxed in an ethanol solution containing 10% hydrochloric acid for 6 h. The solvent was then distilled off and the residue was crystallized from diethyl ether to give methyl 2-oxopropyl 2,6-dimethyl-4-(2-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate as yellow prisms, melting point 155°C (recrystallized from a mixture of ethyl acetate and hexane).

brand name

Bec/Sapresta

Therapeutic Function

Antihypertensive

ARANIDIPINE Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 66)Suppliers
Supplier Tel Email Country ProdList Advantage
ATK CHEMICAL COMPANY LIMITED
+undefined-21-51877795 ivan@atkchemical.com China 32686 60
Shaanxi Dideu Medichem Co. Ltd
+86-029-89586680 +86-18192503167 1026@dideu.com China 9126 58
Dideu Industries Group Limited
+86-29-89586680 +86-15129568250 1026@dideu.com China 28200 58
Dayang Chem (Hangzhou) Co.,Ltd.
571-88938639 +8617705817739 info@dycnchem.com CHINA 52867 58
InvivoChem
+1-708-310-1919 +1-13798911105 sales@invivochem.cn United States 6393 58
TargetMol Chemicals Inc.
+1-781-999-5354 support@targetmol.com United States 19973 58
PT CHEM GROUP LIMITED
+86-85511178 +86-85511178 peter68@ptchemgroup.com China 35453 58
LGM Pharma 1-(800)-881-8210 inquiries@lgmpharma.com United States 2127 70
Hangzhou Yuhao Chemical Technology Co., Ltd 0571-82693216 info@yuhaochemical.com China 9394 52
Shanghai T&W Pharmaceutical Co., Ltd. +86 21 61551611 China 9901 58

View Lastest Price from ARANIDIPINE manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
ARANIDIPINE USP/EP/BP pictures 2021-08-07 ARANIDIPINE USP/EP/BP
86780-90-7
US $1.10 / g 1g 99.9% 100 Tons min Dideu Industries Group Limited
Aranidipine pictures 2020-05-12 Aranidipine
86780-90-7
US $0.00-0.00 / KG 1KG 99.0% 500 MT Shaanxi Dideu Medichem Co. Ltd
  • Aranidipine pictures
  • Aranidipine
    86780-90-7
  • US $0.00-0.00 / KG
  • 99.0%
  • Shaanxi Dideu Medichem Co. Ltd
ARANIDIPINE 2,6-Dimethyl-4-(2-nitrophenyl)-1,4-dihydro-3,5-pyridinedicarboxylic acid methyl 2-oxopropyl ester MPC-1304 Sapresta 1,4-Dihydro-2,6-dimethyl-4-(2-nitrophenyl)-3,5-pyridinedicarboxylic acid 3-methyl 5-(2-oxopropyl) ester Asanidipine 3,5-Pyridinedicarboxylicacid, 1,4-dihydro-2,6-dimethyl-4-(2-nitrophenyl)-, 3-methyl 5-(2-oxopropyl)ester 3-Methyl 5-(2-oxopropyl) 2,6-diMethyl-4-(2-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate Aranidipine MPC1304 ARANIDIPINE MPC1304;MPC-1304;MPC 1304 ARANIDIPINE USP/EP/BP Calcium Channel,inhibit,MPC 1304,Inhibitor,MPC-1304,Aranidipine,Ca channels,Ca2+ channels 86780-90-7