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Merck
CN

859052

N-Hippuryl-His-Leu hydrate

99%, for peptide synthesis

Synonym(s):

N-Benzoyl-Gly-His-Leu, N-Hippuryl-L-histidyl-L-leucine hydrate

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About This Item

Empirical Formula (Hill Notation):
C21H27N5O5 · xH2O
CAS Number:
Molecular Weight:
429.47 (anhydrous basis)
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352209
EC Number:
250-597-9
MDL number:
Beilstein/REAXYS Number:
5664178
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Product Name

N-Hippuryl-His-Leu hydrate, 99%

InChI key

NWOJMNXIJBZMPK-QJHJCNPRSA-N

InChI

1S/C21H27N5O5.H2O/c1-13(2)8-17(21(30)31)26-20(29)16(9-15-10-22-12-24-15)25-18(27)11-23-19(28)14-6-4-3-5-7-14;/h3-7,10,12-13,16-17H,8-9,11H2,1-2H3,(H,22,24)(H,23,28)(H,25,27)(H,26,29)(H,30,31);1H2/t16-,17-;/m0./s1

SMILES string

O.CC(C)C[C@H](NC(=O)[C@H](Cc1c[nH]cn1)NC(=O)CNC(=O)c2ccccc2)C(O)=O

assay

99%

form

powder

optical activity

[α]22/D −41°, c = 1 in 1 M HCl

reaction suitability

reaction type: solution phase peptide synthesis

mp

108-110 °C (dec.)

application(s)

peptide synthesis

Quality Level

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General description

Substrate for angiotensin converting enzyme.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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