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15544

Sigma-Aldrich

Boc-Hyp-OH

≥98.0% (TLC)

Synonym(s):

trans-N-(tert-Butoxycarbonyl)-4-hydroxy-L-proline, Boc-L-hydroxyproline

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About This Item

Empirical Formula (Hill Notation):
C10H17NO5
CAS Number:
Molecular Weight:
231.25
Beilstein/REAXYS Number:
4295484
MDL number:
UNSPSC Code:
12352209
eCl@ss:
32160406
PubChem Substance ID:
NACRES:
NA.22

Quality Level

assay

≥98.0% (TLC)

optical activity

[α]20/D −53.5±2°, c = 1% in DMF

reaction suitability

reaction type: Boc solid-phase peptide synthesis

mp

123-127 °C (lit.)

application(s)

peptide synthesis

SMILES string

CC(C)(C)OC(=O)N1C[C@H](O)C[C@H]1C(O)=O

InChI

1S/C10H17NO5/c1-10(2,3)16-9(15)11-5-6(12)4-7(11)8(13)14/h6-7,12H,4-5H2,1-3H3,(H,13,14)/t6-,7+/m1/s1

InChI key

BENKAPCDIOILGV-RQJHMYQMSA-N

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flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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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