8.54193
L-Pyroglutamic acid pentachlorophenyl ester
Novabiochem®
Synonym(s):
L-Pyroglutamic acid pentachlorophenyl ester, L-Pyroglutamatic acid pentachlorophenyl ester, Pentachlorophenyl pyroglutamate
About This Item
Recommended Products
Quality Level
product line
Novabiochem®
form
powder
reaction suitability
reaction type: solution phase peptide synthesis
manufacturer/tradename
Novabiochem®
mp
185-190 °C
application(s)
peptide synthesis
storage temp.
15-25°C
InChI
1S/C11H6Cl5NO3/c12-5-6(13)8(15)10(9(16)7(5)14)20-11(19)3-1-2-4(18)17-3/h3H,1-2H2,(H,17,18)/t3-/m0/s1
InChI key
ZKGMBAZWQLUSMW-VKHMYHEASA-N
General description
Analysis Note
Appearance of substance (visual): powder
Identity (IR): passes test
Optical rotation α 25/D (c=2% in DMF): 19.0 - 22.0 °
DCU (DC (0003)): ≤ 2 %
To see the solvent systems used for TLC of Novabiochem® products please click here.
Legal Information
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Regulatory Listings
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EU REACH Annex XVII (Restriction List)
Certificates of Analysis (COA)
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Articles
Proline analogues are promising candidates for tuning the biological, pharmaceutical, or physicochemical properties of naturally occuring, as well as de novo designed, linear, and, cyclic peptides.
Proline analogues are promising candidates for tuning the biological, pharmaceutical, or physicochemical properties of naturally occuring, as well as de novo designed, linear, and, cyclic peptides.
Proline analogues are promising candidates for tuning the biological, pharmaceutical, or physicochemical properties of naturally occuring, as well as de novo designed, linear, and, cyclic peptides.
Proline analogues are promising candidates for tuning the biological, pharmaceutical, or physicochemical properties of naturally occuring, as well as de novo designed, linear, and, cyclic peptides.
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