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Sigma-Aldrich

Oxyma Pure

≥99.0% (HPLC), for peptide synthesis, Novabiochem®

Synonyme(s) :

Oxyma Pure, Ethyl cyano(hydroxyimino)acetate

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About This Item

Formule empirique (notation de Hill):
C5H6N2O3
Numéro CAS:
Poids moléculaire :
142.11
Numéro MDL:
Code UNSPSC :
12352126
Numéro de classement CE :
223-351-3
Nomenclature NACRES :
NA.22

product name

Oxyma Pure, Novabiochem®

Niveau de qualité

Gamme de produits

Novabiochem®

Pureté

≥99.0% (HPLC)

Forme

crystalline powder

Capacité de réaction

reaction type: Coupling Reactions

Fabricant/nom de marque

Novabiochem®

Pf

130-132 °C

Application(s)

peptide synthesis

Température de stockage

2-8°C

InChI

1S/C5H6N2O3/c1-2-10-5(8)4(3-6)7-9/h9H,2H2,1H3/b7-4+

Clé InChI

LCFXLZAXGXOXAP-QPJJXVBHSA-N

Description générale

Oxyma Pure (Ethyl cyano(hydroxyimino)acetate) is a non-explosive alternative to the canonical peptide coupling additive N-hydroxybenzotriazole (HOBt). When used in place of HOBt in carbodiimide-mediated peptide bond formation, it provides products in higher yields with less racemization. The combination of Oxyma Pure/diisopropylcarbodiimide (DIC) has proven to be particularly effective in microwave-assisted peptide synthesis.
The generation of toxic hydrogen cyanide (HCN) from the reaction between Oxyma Pure and DIC has been observed. Fortunately, this side reaction can be eliminated by substituting DIC for the more hindered t-butylethylcarbodiimide.

Associated Protocols and Technical Articles
Guide to Selection of Coupling Reagents

Literature references:
[1] R. Subirós-Funosas, et al. (2009) Chem. Eur. J., 15, 9394
[2] J. Collins , et al. (2014) Org . Lett ., 16, 940.
[3] A. D. McFarland (2019) Org. Process Res. Dev., 23, 2099.
[4] S. R. Manne, et al (2022) Org. Process Res. Dev., 26, 2894.

Application

Further applications of Oxyma Pure:
  • Use in the synthesis of difficult peptides.
  • As an acidic modifier to prevent aspartimide formation.

Caractéristiques et avantages

  • Can be used in place of HOBt in carbodiimide-mediated coupling reactions without change of protocol
  • It gives results comparable to HOAt in step-wise solid-phase synthesis
  • Less epimerization than HOBt in fragment condensation reactions

Remarque sur l'analyse

Color (visual): white to slight yellow to beige
Appearance of substance (visual): crystalline powder
Assay (HPLC, area%): ≥ 99.0 % (a/a)
Identity (IR): passes test
Solubility (12,5 mmol in 25 ml DMF): clearly soluble

Informations légales

Novabiochem is a registered trademark of Merck KGaA, Darmstadt, Germany

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable


Certificats d'analyse (COA)

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Consulter la Bibliothèque de documents

Oxyma: An Efficient Additive for Peptide Synthesis to Replace the Benzotriazole-Based HOBt and HOAt with a Lower Risk of Explosion
R. Subiros-Funosas, et al.
Chemistry?A European Journal , 15, 9394-9394 (2009)
Generation of Hydrogen Cyanide from the Reaction of Oxyma (Ethyl Cyano(hydroxyimino)acetate) and DIC (Diisopropylcarbodiimide)
A. D. McFarland
Organic Process Research & Development, 23, 2099-2099 (2019)
tert-Butylethylcarbodiimide as an Efficient Substitute for Diisopropylcarbodiimide in Solid-Phase Peptide Synthesis: Understanding the Side Reaction of Carbodiimides with OxymaPure
S. R. Manne, et al.,
Organic Process Research & Development, 26, 2894-2894 (2022)
Automatic procedures for the synthesis of difficult peptides using oxyma as activating reagent: A comparative study on the use of bases and on different deprotection and agitation conditions
A. Caporale, et al.
Peptides, 102, 38-46 (2018)
High-Efficiency Solid Phase Peptide Synthesis (HE-SPPS)
J. Collins , et al.
Organic Letters, 16, 940-940 (2014)

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