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Key Documents

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N12821

Sigma-Aldrich

4-Nitrobenzyl alcohol

99%

Sinónimos:

(4-Nitrophenyl)methanol, 1-(Hydroxymethyl)-4-nitrobenzene, 4-(Hydroxymethyl)nitrobenzene, 4-Nitrobenzenemethanol, p-(Hydroxymethyl)nitrobenzene, p-Nitrobenzyl alcohol, p-Nitrophenylmethanol

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About This Item

Fórmula lineal:
O2NC6H4CH2OH
Número de CAS:
619-73-8
Peso molecular:
153.14
Beilstein/REAXYS Number:
1424026
EC Number:
210-611-6
MDL number:
MFCD00007376
UNSPSC Code:
12352100
PubChem Substance ID:
24897479
NACRES:
NA.22

assay

99%

form

solid

bp

185 °C/12 mmHg (lit.)

mp

92-94 °C (lit.)

SMILES string

OCc1ccc(cc1)[N+]([O-])=O

InChI

1S/C7H7NO3/c9-5-6-1-3-7(4-2-6)8(10)11/h1-4,9H,5H2

InChI key

JKTYGPATCNUWKN-UHFFFAOYSA-N

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Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Hee-Kyung Kim et al.
Nucleic acids research, 45(5), 2865-2874 (2016-11-02)
Programmed -1 ribosomal frameshifting (-1PRF) is tightly regulated by messenger RNA (mRNA) sequences and structures in expressing two or more proteins with precise ratios from a single mRNA. Using single-molecule fluorescence resonance energy transfer (smFRET) between (Cy5)EF-G and (Cy3)tRNALys, we
K D James et al.
Journal of bacteriology, 182(11), 3136-3141 (2000-05-16)
Pseudomonas sp. strain TW3 is able to metabolize 4-nitrotoluene to 4-nitrobenzoate and toluene to benzoate aerobically via a route analogous to the upper pathway of the TOL plasmids. We report the cloning and characterization of a benzyl alcohol dehydrogenase gene
Janghyun Yoo et al.
Nature communications, 11(1), 3336-3336 (2020-07-06)
We describe theory, experiments, and analyses of three-color Förster resonance energy transfer (FRET) spectroscopy for probing sub-millisecond conformational dynamics of protein folding and binding of disordered proteins. We devise a scheme that uses single continuous-wave laser excitation of the donor
Roger B Altman et al.
Nature methods, 9(1), 68-71 (2011-11-15)
Fluorescence applications requiring high photostability often depend on the use of solution additives to enhance fluorophore performance. Here we demonstrate that the direct or proximal conjugation of cyclooctatetraene (COT), 4-nitrobenzyl alcohol (NBA) or Trolox to the cyanine fluorophore Cy5 dramatically
Richa Dave et al.
Biophysical journal, 96(6), 2371-2381 (2009-03-18)
Organic fluorophores common to fluorescence-based investigations suffer from unwanted photophysical properties, including blinking and photobleaching, which limit their overall experimental performance. Methods to control such processes are particularly important for single-molecule fluorescence and fluorescence resonance energy transfer imaging where uninterrupted
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