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Safety Information

09794

Sigma-Aldrich

Boc-β-Phe-OH

≥96.0% (HPLC)

Synonym(s):

(R)-3-(Boc-amino)-3-phenylpropionic acid, Boc-L-β-phenylalanine

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About This Item

Empirical Formula (Hill Notation):
C14H19NO4
CAS Number:
161024-80-2
Molecular Weight:
265.30
Beilstein:
5404389
MDL number:
MFCD01320859
UNSPSC Code:
12352200
PubChem Substance ID:
329748832
NACRES:
NA.26

Quality Level

100

Assay

≥96.0% (HPLC)

application(s)

peptide synthesis

SMILES string

CC(C)(C)OC(=O)N[C@H](CC(O)=O)c1ccccc1

InChI

1S/C14H19NO4/c1-14(2,3)19-13(18)15-11(9-12(16)17)10-7-5-4-6-8-10/h4-8,11H,9H2,1-3H3,(H,15,18)(H,16,17)/t11-/m1/s1

InChI key

JTNQFJPZRTURSI-LLVKDONJSA-N

Application

Boc-L-β-Phenylalanine is an N-terminal protected amino acid used in solid-phase peptide synthesis (SPPS) to make peptides containing β-phenylalanine residues.

Biochem/physiol Actions

Boc-L-β-phenylalanine may be useful in the synthesis of anti-microbial β-peptides.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

09794-VAR:
09794-1G:
09794-BULK:
09794-250MG:

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Certificates of Analysis (COA)

Lot/Batch Number
452966/1
433034/1
431699/1
401732/1

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Jagannath Mondal et al.
The journal of physical chemistry. B, 114(42), 13585-13592 (2010-10-05)
Recent experimental studies have revealed interesting sequence dependence in the antimicrobial activity of β-peptides, which suggests the possibility of a rational design of new antimicrobial agents. To obtain insight into the mechanism of membrane activity, we present a computer simulation

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