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8.53045

Sigma-Aldrich

Boc-Asp(OBzl)-OH

Novabiochem®

Synonym(s):

Boc-Asp(OBzl)-OH, N-α-t.-Boc-L-aspartic acid β-benzyl ester

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About This Item

Empirical Formula (Hill Notation):
C16H21NO6
CAS Number:
Molecular Weight:
323.34
MDL number:
UNSPSC Code:
12352209
EC Index Number:
231-406-8
NACRES:
NA.22

Quality Level

product line

Novabiochem®

Assay

≥98% (TLC)

form

powder

reaction suitability

reaction type: Boc solid-phase peptide synthesis

manufacturer/tradename

Novabiochem®

application(s)

peptide synthesis

functional group

carboxylic acid

storage temp.

2-30°C

InChI

1S/C16H21NO6/c1-16(2,3)23-15(21)17-12(14(19)20)9-13(18)22-10-11-7-5-4-6-8-11/h4-8,12H,9-10H2,1-3H3,(H,17,21)(H,19,20)

InChI key

SOHLZANWVLCPHK-UHFFFAOYSA-N

General description

Building block for introduction of aspartic acid amino-acid residues by Boc SPPS.

Associated Protocols and Technical Articles
Cleavage and Deprotection Protocols for Boc SPPS

Linkage

Replaces: 04-12-0028

Analysis Note

Colour (visual): white to off white
Appearance of substance (visual): powder
Identity (IR): conforms
Optical rotation α 25/D (c=2 AcOH): +7.5 - +9.5 °
Purity
- TLC(011A): ≥ 98 %
- TLC(0811): ≥ 98 %
Solubility (1 mmole in 2 ml DMF): clearly soluble

To see the solvent systems used for TLC of Novabiochem® products please click here.

Legal Information

Novabiochem is a registered trademark of Merck KGaA, Darmstadt, Germany

related product

Product No.
Description
Pricing

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Certificates of Analysis (COA)

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Protocols

Anhydrous HF is the preferred reagent for peptide cleavage from Boc-based resins, versatile and effective for various peptide synthesis.

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

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