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Catalog Number:
38047
CAS Number:
89226-75-5
Manidipine dihydrochloride
Purity:
98 - 101% (Assay)
Synonym(s):
1,4-Dihydro-2,6-dimethyl-4-(3-nitrophenyl)-3,5-pyridinedicarboxylic acid 2-[4-(Diphenylmethyl)-1-piperazinyl]ethyl methyl ester dihydrochloride, 2-[4-(Diphenylmethyl)-1-piperazinyl]ethyl methyl 1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)-3,5-pyridinedicarboxylate dihydrochloride
Hazmat
Documents
$181.67 /1G
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Product Information
Synonyms
1,4-Dihydro-2,6-dimethyl-4-(3-nitrophenyl)-3,5-pyridinedicarboxylic acid 2-[4-(Diphenylmethyl)-1-piperazinyl]ethyl methyl ester dihydrochloride, 2-[4-(Diphenylmethyl)-1-piperazinyl]ethyl methyl 1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)-3,5-pyridinedicarboxylate dihydrochloride
CAS Number
89226-75-5
Purity
98 - 101% (Assay)
Molecular Formula
C35H38N4O6·2HCl
Molecular Weight
0
MDL Number
MFCD00896434
PubChem ID
150762
Melting Point
~207 °C (dec.)
Appearance
Yellow or light yellow crystalline
Conditions
Store at 2 - 8 °C
General Information
Synonyms
1,4-Dihydro-2,6-dimethyl-4-(3-nitrophenyl)-3,5-pyridinedicarboxylic acid 2-[4-(Diphenylmethyl)-1-piperazinyl]ethyl methyl ester dihydrochloride, 2-[4-(Diphenylmethyl)-1-piperazinyl]ethyl methyl 1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)-3,5-pyridinedicarboxylate dihydrochloride
CAS Number
89226-75-5
Purity
98 - 101% (Assay)
Molecular Formula
C35H38N4O6·2HCl
Molecular Weight
0
MDL Number
MFCD00896434
PubChem ID
150762
Melting Point
~207 °C (dec.)
Appearance
Yellow or light yellow crystalline
Conditions
Store at 2 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Yes
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Manidipine dihydrochloride is widely utilized in research focused on:

  • Hypertension Treatment: This compound is primarily used in the pharmaceutical industry for managing high blood pressure, providing effective vasodilation and reducing cardiovascular risks.
  • Cardiovascular Research: Researchers often explore its effects on heart health, studying its mechanisms to improve blood flow and reduce strain on the heart.
  • Combination Therapies: It is frequently combined with other antihypertensive agents to enhance therapeutic efficacy, allowing for lower doses and reduced side effects.
  • Drug Development: In the field of medicinal chemistry, it serves as a model compound for developing new antihypertensive medications, guiding the design of more effective and safer drugs.
  • Clinical Trials: Manidipine dihydrochloride is often involved in clinical studies to assess its long-term effects and benefits, contributing valuable data to the medical community.

Citations