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158014-03-0

158014-03-0 Structure

158014-03-0 Structure
IdentificationBack Directory
[Name]

Ethyl (hydroxyimino)cyanoacetate potassium salt
[CAS]

158014-03-0
[Synonyms]

K-Oxyma
K-Oxyma 97%
K-Oxyma Pure
K-OXYMA PURE 25 G
K-Oxyma≥ 99% (HPLC)
OxymaPurepotassiumsalt
K-Oxyma Pure Novabiochem
Ethyl (hydroxyimino)cyanoacetate potassium
Ethyl (hydroxyimino)cyanoacetate potassium salt
Ethyl 2-cyano-2-(hydroxyimino)acetate, potassium salt
Cyano(hydroxyimino)acetic acid ethyl ester potassium salt
Cyano-2-(hydroxyimino)acetic acid ethyl ester potassium salt
2-Cyano-2-(hydroxyimino)acetic acid ethyl ester, potassium salt
2-Cyano-2-(hydroxyimino)acetic acid ethyl ester potassium salt (1:1)
2-Cyano-2-(hydroxyimino)acetic Acid Ethyl Ester Potassium Salt (K-OXYMA)
[Molecular Formula]

C5H5KN2O3
[MDL Number]

MFCD26960809
[MOL File]

158014-03-0.mol
[Molecular Weight]

180.203
Chemical PropertiesBack Directory
[Melting point ]

145-155°C
[storage temp. ]

2-8°C
[solubility ]

Methanol (Slightly), Water (Sparingly)
[form ]

Solid
[color ]

Dark Yellow
Safety DataBack Directory
[Hazard Codes ]

T
[Risk Statements ]

20/21-25-43
[Safety Statements ]

36/37-45
[RIDADR ]

UN 3439 6.1 / PGIII
[WGK Germany ]

3
[HS Code ]

2928 00 90
Hazard InformationBack Directory
[Chemical Properties]

Bright yellow powder
[Uses]

  • Non-explosive replacement for HOBt and HOAt with at least comparable performance to HOAt
  • Outperforms HOAt in sterically demanding peptide bond formations
  • Compatible with carbodiimide-mediated; solution and solid phase peptide coupling;
  • Less epimerization than HOBt in fragment condensation reactions
  • K-salt especially useful in peptide coupling on mild acid-labile resins such as 2-chlorotrityl; leading to minimal to no cleavage of the peptide from the resin due to its more alkaline character
  • K-salt has a higher melting point than OxymaPure
[Uses]

Ethyl (hydroxyimino)cyanoacetate potassium salt is a Non-explosive replacement for HOBt and HOAt with at least comparable performance to HOAt Outperforms HOAt in sterically demanding peptide bond formations Compatible with carbodiimide-mediated; solution and solid phase peptide coupling; Less epimerization than HOBt in fragment condensation reactions K-salt especially useful in peptide coupling on mild acid-labile resins such as 2-chlorotrityl; leading to minimal to no cleavage of the peptide from the resin due to its more alkaline character K-salt has a higher melting point than OxymaPure.
[Uses]

Useful in peptide coupling on mild acid-labile resins with minimal to no cleavage of the peptide from the resin due to its more alkaline character. This can be used to replace the explosive HOBt and HOAt.
[reaction suitability]

reaction type: Coupling Reactions
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