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72800

Supelco

4-Nitrobenzaldehyde

for spectrophotometric det. of amino sugars, ≥99.0%

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About This Item

Linear Formula:
O2NC6H4CHO
CAS Number:
555-16-8
Molecular Weight:
151.12
Beilstein:
386796
EC Number:
209-084-5
MDL number:
MFCD00007346
UNSPSC Code:
12000000
PubChem Substance ID:
329764369
NACRES:
NA.21

Quality Level

100

Assay

≥99.0% (HPLC)
≥99.0%

form

powder

quality

for spectrophotometric det. of amino sugars

technique(s)

UV/Vis spectroscopy: suitable

ign. residue

≤0.05%

mp

103-106 °C (lit.)
104-106 °C

SMILES string

[O-][N+](=O)c1ccc(C=O)cc1

InChI

1S/C7H5NO3/c9-5-6-1-3-7(4-2-6)8(10)11/h1-5H

InChI key

BXRFQSNOROATLV-UHFFFAOYSA-N

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Other Notes

Reagent for the spectrophotometric det. of amino carbohydrates[1]

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H317,H319

Hazard Classifications

Eye Irrit. 2 - Skin Sens. 1

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Benzaldehyde purified by redistillation, ≥99.5%

Sigma-Aldrich

418099

Benzaldehyde

A. Nakamura et al.
Chemical & Pharmaceutical Bulletin, 17, 770-770 (1969)
Mikhail Yu Karganov et al.
Biological trace element research, 198(2), 567-574 (2020-03-08)
The objective of the present study was investigation of tissue trace element distribution in a streptozotocin model of DM1 in rats. DM1 was modeled in 2-month-old male Wistar rats (n = 30) using intraperitoneal injection of 45 mg/kg b.w. (STZ1) and 55 mg/kg b.w.
H Maheswaran et al.
Chemical communications (Cambridge, England), (39)(39), 4066-4068 (2006-10-07)
The dichloro[(-)-sparteine-N,N']copper(II) complex provides Henry adducts with high enantioselectivities (73-97% ee) in Henry reaction between nitromethane and various aldehydes.
Chao Li et al.
Journal of biotechnology, 150(4), 539-545 (2010-10-21)
Several proteases, especially pepsin, were observed to directly catalyze asymmetric aldol reactions. Pepsin, which displays well-documented proteolytic activity under acidic conditions, exhibited distinct catalytic activity in a crossed aldol reaction between acetone and 4-nitrobenzaldehyde with high yield and moderate enantioselectivity.
Jinmo Kim et al.
Analytical chemistry, 77(13), 4137-4141 (2005-07-01)
A chemical derivatization technique in time-of-flight secondary ion mass spectrometry (TOF-SIMS) has been developed to quantify the surface density of amine groups of plasma-polymerized ethylenediamine thin film deposited on a glass surface by inductively coupled plasma chemical vapor deposition. Chemical
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