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42100

Supelco

Nα-(2,4-Dinitro-5-fluorophenyl)-D-valinamide

for chiral derivatization, LiChropur, ≥98.0%

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About This Item

Empirical Formula (Hill Notation):
C11H13FN4O5
CAS Number:
Molecular Weight:
300.24
MDL number:
UNSPSC Code:
41116105
PubChem Substance ID:
NACRES:
NA.22

grade

for chiral derivatization

Quality Level

Assay

≥98.0% (sum of enantiomers, HPLC)
≥98.0%

form

solid

optical activity

[α]20/D −14.0±1.5°, c = 2% in acetone

optical purity

enantiomeric ratio: ≥99.5:0.5 (HPLC)

quality

LiChropur

technique(s)

HPLC: suitable

mp

173-177 °C

storage temp.

2-8°C

SMILES string

CC(C)[C@@H](Nc1cc(F)c(cc1[N+]([O-])=O)[N+]([O-])=O)C(N)=O

InChI

1S/C11H13FN4O5/c1-5(2)10(11(13)17)14-7-3-6(12)8(15(18)19)4-9(7)16(20)21/h3-5,10,14H,1-2H3,(H2,13,17)/t10-/m1/s1

InChI key

ZTFFRKNPAXXEBL-SNVBAGLBSA-N

General description

Nα-(2,4-Dinitro-5-fluorophenyl)-D-valinamide [D-FDVA] is a derivatizing agent.

Application

D-FDVA may be used as derivatizing agent for nullifying the possibility of minor compounds to be diastereomer of xenortide A, during HPLC-MS screening.

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Legal Information

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

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

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

42100-VAR:
42100-BULK:
42100-100MG:
42100-500MG:


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Gerhard Lang et al.
Journal of natural products, 71(6), 1074-1077 (2008-05-22)
Three new peptides, xenortides A and B and xenematide, were isolated from a culture of the nematode-associated entomopathogenic bacterium Xenorhabdus nematophilus. Their structures were elucidated using NMR, MS, and chemical derivatization methods. Xenortides A and B are the N-phenethylamide and

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