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Home > products > API Active Pharmaceutical Ingredient > White To Beige Solid Benazepril CAS 86541-75-5

White To Beige Solid Benazepril CAS 86541-75-5

Product Details

Place of Origin: China

Brand Name: Sunshine

Certification: ISO,COA

Model Number: 86541-75-5

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Minimum Order Quantity: Negotiation

Price: Negotiation

Packaging Details: Bag,Drum

Delivery Time: 7-15 days

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Benazepril CAS 86541-75-5

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CAS 86541-75-5

CAS NO::
86541-75-5
Appearance::
White To Beige Solid
Molecular Formula::
C24H28N2O5
Molecular Weight::
424.49000
EINECS NO::
NA
MDL NO::
MFCD00864466
CAS NO::
86541-75-5
Appearance::
White To Beige Solid
Molecular Formula::
C24H28N2O5
Molecular Weight::
424.49000
EINECS NO::
NA
MDL NO::
MFCD00864466
White To Beige Solid Benazepril CAS 86541-75-5

Product Description:

Product Name: Benazepril CAS NO: 86541-75-5

 

 

Synonyms:

Benazepril [INN:BAN];

2-[(3S)-3-[[(2S)-1-ethoxy-1-oxo-4-phenylbutan-2-yl]amino]-2-oxo-4,5-dihydro-3H-1-benzazepin-1-yl]acetic acid;

(3S)-1-(carboxymethyl)-[[(1S)-1-(ethoxycarbonyl)-3-phenylpropyl]amino]-2,3,4,5-tetrahydro-1H-[1]benzazepin-2-one;

 

 

Chemical & Physical Properties:

Appearance:White to beige solid

Assay :≥99.0%

Density: 1.26g/cm3

Boiling Point: 691.2℃ at 760 mmHg

Melting Point: 148 – 149℃

Flash Point: 371.8℃

Refractive Index: 1.607

Storage Condition: Store in original container in a cool dark place.

Vapor Pressure: 4.69E-20mmHg at 25℃

 

 

Safety Information:

Safety Statements: S22-S24/25

 

 

Benazepril, brand name Lotensin (Novartis), is an ACE inhibitor used primarily in treatment of hypertension, congestive heart failure, and heart attacks, and also in preventing the renal and retinal complications of diabetes.

ACE inhibitors relax blood vessels, and decrease blood volume, which lowers blood pressure and decreases oxygen demand from the heart. They inhibit angiotensin-converting enzyme, which is part of the renin–angiotensin–aldosterone system.

Benazepril is a prodrug which is metabolized by the liver into its active form benazeprilat via cleavage of the drug's ester group.

 

 

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