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Sigma-Aldrich

(S)-5-Azido-2-(Fmoc-amino)pentanoic acid

≥97.0% (HPLC), for peptide synthesis

Synonym(s):

Fmoc-5-azido-L-norvaline, Fmoc-L-δ-azidoornithine, Fmoc-Orn(N2)-OH

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About This Item

Empirical Formula (Hill Notation):
C20H20N4O4
CAS Number:
Molecular Weight:
380.40
MDL number:
UNSPSC Code:
12352209
PubChem Substance ID:
NACRES:
NA.26

product name

(S)-5-Azido-2-(Fmoc-amino)pentanoic acid, ≥97.0% (HPLC)

Assay

≥97.0% (HPLC)

form

powder

optical activity

[α]/D 3.5±0.3°, c = 1 in ethyl acetate

composition

carbon, 62.2-63.9%
nitrogen, 14.3-15.1%

reaction suitability

reaction type: Fmoc solid-phase peptide synthesis
reaction type: click chemistry

application(s)

peptide synthesis

functional group

Fmoc

storage temp.

2-8°C

SMILES string

OC(=O)[C@H](CCCN=[N+]=[N-])NC(=O)OCC1c2ccccc2-c3ccccc13

InChI

1S/C20H20N4O4/c21-24-22-11-5-10-18(19(25)26)23-20(27)28-12-17-15-8-3-1-6-13(15)14-7-2-4-9-16(14)17/h1-4,6-9,17-18H,5,10-12H2,(H,23,27)(H,25,26)/t18-/m0/s1

InChI key

TVPIDQLSARDIPX-SFHVURJKSA-N

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

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

Certificates of Analysis (COA)

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Lucio Litti et al.
Nanoscale, 10(3), 1272-1278 (2018-01-03)
Multimodal contrast agents offer new interesting diagnostic possibilities, summing the benefits of multiple imaging techniques. Magnetic resonance and optical imaging are complementary techniques. The first allows total body screening, even though it suffers from low spatial resolution and needs high

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