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Suc-Pro-OH

Suc-Pro-OH is a proline-derived amino acid derivative in which the proline nitrogen is acylated with a succinyl (Suc) group, yielding a protected proline carboxylic acid (free -COOH) rather than a free amino acid. The molecule contains a secondary amide (succinylated N) and retains the amino acid backbone functionality with an unprotected carboxyl group, while the proline ring provides a cyclic side chain that constrains conformational flexibility. Suc-Pro-OH is used as a precursor for preparing more complex proline-containing amino acid and peptide derivatives, including stepwise assembly where temporary masking of the amino functionality supports controlled coupling chemistry.

Designed for biological research and industrial applications, not intended for individual clinical or medical purposes.

CAT No: CP27300

CAS No:63250-32-8

Synonyms/Alias:methyl2-amino-4-methylpentanoatehydrochloride;6322-53-8;MethylL-leucinatehydrochloride;SBB003738;L-leucinemethylester;methyl2-azanyl-4-methyl-pentanoatehydrochloride;2-amino-4-methylpentanoicacidmethylesterhydrochloride;H-DL-Leu-Ome-HCl;MethylL-leucinateHCl;L-Leucine,hydrochloride;AC1MJ1QK;ACMC-209m4m;ACMC-209ox7;AC1Q3BV3;H-DL-Leu-OMehydrochloride;SCHEMBL355415;CTK8B3449;MolPort-002-497-761;NSC32110;EINECS231-375-0;ANW-42539;KM0720;NSC-32110;NSC522233;NSC522846

Custom Peptide Synthesis
cGMP Peptide
  • Registration of APIs
  • CMC information required for an IND
  • IND and NDA support
  • Drug master files (DMF) filing
M.F/Formula
C7H16ClNO2
M.W/Mr.
215.21
Source#
Synthetic
Size
1 g;5 g;
InChI
1S/C7H15NO2.ClH/c1-5(2)4-6(8)7(9)10-3;/h5-6H,4,8H2,1-3H3;1H
InChI Key
DODCBMODXGJOKD-UHFFFAOYSA-N
Canonical SMILES
CC(C)CC(C(=O)OC)N.Cl

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