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Merck
CN

N1018

3-Nitro-L-tyrosine ethyl ester hydrochloride

≥99% (titration)

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About This Item

Empirical Formula (Hill Notation):
C11H14N2O5 · HCl
CAS Number:
Molecular Weight:
290.70
UNSPSC Code:
12352200
PubChem Substance ID:
EC Number:
266-466-4
MDL number:
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InChI key

GITKQXFBNJTMRP-QRPNPIFTSA-N

InChI

1S/C11H14N2O5.ClH/c1-2-18-11(15)8(12)5-7-3-4-10(14)9(6-7)13(16)17;/h3-4,6,8,14H,2,5,12H2,1H3;1H/t8-;/m0./s1

SMILES string

Cl.CCOC(=O)[C@@H](N)Cc1ccc(O)c(c1)[N+]([O-])=O

assay

≥99% (titration)

form

powder

color

yellow

mp

185 °C

application(s)

peptide synthesis

storage temp.

2-8°C

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Biochem/physiol Actions

3-Nitro-L-tyrosine ethyl ester hydrochloride or NTEE is used measure enzyme activity following carboxylate modification.

Storage Class

13 - Non Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Information

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S K Niture et al.
European journal of biochemistry, 268(3), 832-840 (2001-02-13)
Fusarium moniliforme NCIM 1276 isolated from a tropical mangrove ecosystem produces a single extracellular endo-polygalacturonase with an M(r) of 38 kDa and a carbohydrate content of 4%. It has an alkaline pI of 8.1. The K(m) is 0.12 mg.mL(-1), V(max)
Guinevere Strack et al.
The journal of physical chemistry. B, 113(35), 12154-12159 (2009-08-12)
The biochemical system logically processing biochemical signals using immune-specific and biocatalytic reactions was designed, and the generated output signals were analyzed by AFM and optical means. Different patterns of immune signals resulted in the formation of various interfacial structures followed

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