Anaesthetic drugs & related adjuncts & analeptics

Other Notes Please note that Sigma-Aldrich provides this product to early discovery researchers as part of a collection of unique chemicals. Sigma-Aldrich does not collect analytical data for this product.

We are committed to bringing you Greener Alternative Products, which adhere to one of the four categories of Greener Alternatives . This product belongs to category of Re-engineered products, showing key improvements in Green Chemistry Principles

We are committed to bringing you Greener Alternative Products, which adhere to one of the four categories of Greener Alternatives . This product belongs to category of Re-engineered products, showing key improvements in Green Chemistry Principles

EMPLURA &#174 is our low-cost alternative to high-purity qualities. With EMPLURA we offer a range of solvents for a plurality of basic applications in non-regulated industries and for less demanding applications, preparative laboratory work and

EMSURE grade solvents are suitable for a broad spectrum of classical lab applications, and are frequently used in regulated and highly demanding lab applications. EMSURE provides worldwide best and most extensive product specifications.

EMSURE grade solvents are suitable for a broad spectrum of classical lab applications, and are frequently used in regulated and highly demanding lab applications. EMSURE provides worldwide best and most extensive product specifications.

EMSURE grade solvents are suitable for a broad spectrum of classical lab applications, and are frequently used in regulated and highly demanding lab applications. EMSURE provides worldwide best and most extensive product specifications.

Other Notes Please note that Sigma-Aldrich provides this product to early discovery researchers as part of a collection of unique chemicals. Sigma-Aldrich does not collect analytical data for this product.

Application Reactant for: Synthesis of multiprotected kanosamine Selective acylation in peptide synthesis Reagent for: Stereoselective aldol condensation reactions for synthesis of &#946-lactam antibiotics Diastereoselective synthesis of aldols

Application Reactant for: Synthesis of multiprotected kanosamine Selective acylation in peptide synthesis Reagent for: Stereoselective aldol condensation reactions for synthesis of &#946-lactam antibiotics Diastereoselective synthesis of aldols

Other Notes Please note that Sigma-Aldrich provides this product to early discovery researchers as part of a collection of unique chemicals. Sigma-Aldrich does not collect analytical data for this product.

Analysis Note Assay (GC, area%): &#8805 99.0 % (a/a) Melting range (lower value): &#8805 48 &#176C Melting range (upper value): &#8804 50 &#176C 2-Naphthylamine (GC, area%): &#8804 0.