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About This Item
Linear Formula:
O2NC6H4CH2CH(NH2)CO2H
CAS Number:
Molecular Weight:
210.19
EC Number:
MDL number:
UNSPSC Code:
12352209
eCl@ss:
32160406
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
98%
form
powder
reaction suitability
reaction type: solution phase peptide synthesis
mp
236-237 °C (dec.) (lit.)
application(s)
peptide synthesis
SMILES string
NC(Cc1ccc(cc1)[N+]([O-])=O)C(O)=O
InChI
1S/C9H10N2O4/c10-8(9(12)13)5-6-1-3-7(4-2-6)11(14)15/h1-4,8H,5,10H2,(H,12,13)
InChI key
GTVVZTAFGPQSPC-UHFFFAOYSA-N
Related Categories
Application
4-Nitro-DL-phenylalanine may be used as an internal standard for the determination of β-N-methylamino-L-alanine (L-BMAA) in environmental aqueous samples using proton nuclear magnetic resonance (1H NMR) technique.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 3 Oral
Storage Class Code
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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M Balbaa et al.
The International journal of biochemistry, 26(1), 35-42 (1994-01-01)
1. The tetrapeptide Ala2-Nph2 (where Nph = p-nitrophenylalanyl) is treated by porcine pepsin to study the mechanism of aminotranspeptidation reactions. 2. The major initial product is Ala2-Nph and the major transpeptidation products are Nph2 and Nph3 accompanied by some Nph
G Giammanco et al.
Microbiologica, 8(4), 395-397 (1985-10-01)
A rapid test for detection of p-nitrophenylalanine ammonia-lyase is described. The test is performed by suspending a loopful of bacteria in 0.5 ml of a buffered 1 mM solution of p-nitro-DL-phenylalanine (PNPA). The enzymatic activity is revealed by the formation
Meng-Lin Tsao et al.
Journal of the American Chemical Society, 128(14), 4572-4573 (2006-04-06)
The unnatural amino acid p-nitrophenylalanine (pNO2-Phe) was genetically introduced into proteins in Escherichia coli in response to the amber nonsense codon with high fidelity and efficiency by means of an evolved tRNA/aminoacyl-tRNA synthetase pair from Methanocuccus jannaschii. It was shown
1H NMR determination of ?-N-methylamino-l-alanine (l-BMAA) in environmental and biological samples.
Moura S, et al.
Toxicon, 53(5), 578-583 (2009)
Masumi Taki et al.
Journal of the American Chemical Society, 124(49), 14586-14590 (2002-12-06)
Four-base codon strategy was applied to incorporate a fluorophore-quencher pair into specific positions on a single protein; beta-anthraniloyl-L-alpha,beta-diaminopropionic acid (atnDap) was employed as a fluorophore and p-nitrophenylalanine (ntrPhe) as a quencher. Their positions were directed by the CGGG/CCCG and GGGC/CCCG
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