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To produce highly pure (S, S)-NEPA, it requires sophisticated technologies to separate three other optical isomers for the utmost optical purity. Everlight has succeeded in the key technologies of hydrogenation and asymmetric synthesis for producing (S, S)-NEPA. Quality The
purity of our pharmaceutical intermediate, (S, S)-NEPA,
is ≥ 98.5%. The (R, S)-isomer impurities are <
0.5%. More importantly, the impurity Cyclohexyl-NEPA is
less than 0.2%. However, these optical and chemical
isomers of (S, S)-NEPA, are available for our
customers’ analytical and development needs. Table
I. The Worldwide Sales of ACE Inhibitors1
Unit:USD,
millions
*
Estimated The
demand of (S, S)-NEPA has been increasing during the
past few years, and it will continue to grow in the near
future. However, the quantity of ACE Inhibitor depends
closely on the optical quality of this key intermediate.
Although Enalapril Maleate2,3 (Vasotec®
) world sales are slipping, the combined formulations,
Lexxel®3 (Enalapril Maleate &
Felodipine), Vaseretic® (Enalapril Maleate & Hydrochlorothiazide)3,
Teczem® (Enalapril Maleate & Diltiazem Maleate)3
have been increasing in the treatment of hypertension
& CHF due to lower side effects and better therapy
results. Another
New Intermediate From Everlight ---
NEPA-NCA In addition, another key intermediate for ACE inhibitor, NEPA-NCA (chemical name: N- [1-(S)- Ethoxycarbonyl -3-Phenylpropyl] -(S)- Alanine- N-Carboxyanhydride ), is also available commercially. The assay is between 98.0 ~ 102.0% with total impurities less than 0.5%. Reference 1.
Med Ad News1998/1999 2.
Martindale 31 Edition 3.
Physicians’ Desk Reference
52 Edition, 1998 |
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Everlight Chemical Industrial
Corporation 6th Fl, 77, Tun Hua South Road, Sec.2, Taipei, Taiwan 106 TEL : 886-2-27066006 FAX : 886-2-27081254 e-mail : webmaster@ecic.com |
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