Chemodex

(+)-Naproxen methyl ester

CHF 84.00
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CDX-N0557-M05050 mgCHF 84.00
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Product Details
Synonyms (S)-Naproxen methyl ester; NME; Naproxen Impurity E (PhEur); (2S)-2-(6-Methoxy-2-naphthyl)propionic acid methyl ester; Methyl (2S)-2-(6-Methoxynaphthalen-2-yl)propanoat
Product Type Chemical
Properties
Formula C15H16O3
MW 244.29
CAS 26159-35-3
Source/Host Chemicals Synthetic
Purity Chemicals ≥98% (HPLC)
Appearance White to off-white powder or crystals.
Solubility Soluble in chloroform, methanol or DCM.
Identity Determined by 1H-NMR.
Declaration Manufactured by Chemodex.
Other Product Data

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Our product description may differ slightly from the original manufacturers product datasheet.

InChi Key ZFYFBPCRUQZGJE-UHFFFAOYSA-N
Smiles C(C(OC)=O)(C)C1=CC2=C(C=C(OC)C=C2)C=C1
Shipping and Handling
Shipping AMBIENT
Short Term Storage +20°C
Long Term Storage +4°C
Handling Advice Protect from light and moisture.
Use/Stability Stable for at least 2 years after receipt when stored at +4°C.
Documents
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Product Specification Sheet
Datasheet Download PDF
Description

The metabolite Naproxen methyl ester (Naproxen Impurity E) is a degradation product from Naproxen which is a non-steroidal anti-inflammatory drug (NSAID) used to in the treatment of pain, menstrual cramps, inflammatory diseases such as rheumatoid arthritis, gout and fever. Ibuprofen is an anti-inflammatory COX inhibitor. This product can be used as a control esterase substrate, as a working standard or secondary analytical reference standard or as an organic building block and intermediate for synthesis.

Product References

(1) M. Najlah, et al.; Int. J. Pharm. 308, 175 (2006) | (2) H. Weber, et al.; Arch. Pharm. 327, 337 (1994) | (3) C.J. Welch, et al.; J. High Resol. Chromatogr. 20, 179 (1997) | (4) H. Weber, et al.; Pharma. Res. 18, 600 (2001) | (5) J. Krzek & M. Starek; J. Plan. Chromatogr. 17, 137 (2004) | (6) L. Steenkamp & D. Brady; Proc. Biochem. 43, 1419 (2008) | (7) K.C. Duggan, et al.; J. Biol. Chem. 285, 34950 (2010) | (8) R.S. Reddy, et al.; TACL 6, 55 (2016) | (9) I. Cacciatore, et al.; Int. J. Mol. Sci. 17, 1035 (2016) | (10) K. Birgul, et al.; Eur. J. Med. Chem. 208, 112841 (2020)

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