612510
1,2-Dichlorobenzene solution
suitable for NMR (reference standard), 5% in acetone-d6 (99.9 atom % D), NMR tube size 5 mm × 8 in.
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About This Item
Empirical Formula (Hill Notation):
C6H4Cl2
CAS Number:
Molecular Weight:
147.00
NACRES:
NA.12
PubChem Substance ID:
UNSPSC Code:
12190000
MDL number:
InChI
1S/C6H4Cl2/c7-5-3-1-2-4-6(5)8/h1-4H
SMILES string
Clc1ccccc1Cl
InChI key
RFFLAFLAYFXFSW-UHFFFAOYSA-N
concentration
5% in acetone-d6 (99.9 atom % D)
technique(s)
NMR: suitable
NMR tube size
5 mm × 8 in.
suitability
suitable for NMR (reference standard)
Quality Level
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Related Categories
Features and Benefits
1H resolution
Preparation Note
5 mm O.D. tube contains 0.700 mL.
signalword
Danger
hcodes
Hazard Classifications
Aquatic Chronic 2 - Eye Irrit. 2 - Flam. Liq. 2 - Skin Sens. 1 - STOT SE 3
target_organs
Central nervous system
supp_hazards
Storage Class
3 - Flammable liquids
wgk
WGK 2
flash_point_f
1.4 °F - closed cup
flash_point_c
-17 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves
Regulatory Information
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Sungmin Chin et al.
Chemosphere, 75(9), 1206-1209 (2009-03-10)
This study examined the catalytic oxidation of 1,2-dichlorobenzene on V(2)O(5)/TiO(2) nanoparticles. The V(2)O(5)/TiO(2) nanoparticles were synthesized by the thermal decomposition of vanadium oxytripropoxide and titanium tetraisopropoxide. The effects of the synthesis conditions, such as the synthesis temperature and precursor heating
Ivan Guryanov et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 15(46), 12837-12845 (2009-10-23)
The effect of microwave (MW) irradiation and ionic liquids (IL) on the cycloaddition of azomethine ylides to [60]fullerene has been investigated by screening the reaction protocol with regard to the IL medium composition, the applied MW power, and the simultaneous
Eranda Maligaspe et al.
The journal of physical chemistry. A, 114(1), 268-277 (2009-11-26)
Singlet-singlet energy transfer in self-assembled via axial coordination of imidazole-appended (at different positions of one of the meso-phenyl entities) free-base tetraphenylporphyrin, H(2)PIm, to either zinc phthalocyanine, ZnPc, or zinc naphthalocyanine, ZnNc, dyads is investigated in noncoordinating solvents, o-dichlorobenzene and toluene
Bimalendu Adhikari et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 17(41), 11488-11496 (2011-09-29)
The N-terminally pyrene-conjugated oligopeptide, Py-Phe-Phe-Ala-OMe, (Py=pyrene 1-butyryl acyl) forms transparent, stable, supramolecular fluorescent organogels in various organic solvents. One of these organogels was thoroughly studied using various techniques including transmission electron microscopy (TEM), field-emission scanning electron microscopy (FESEM), atomic force
Eric Vejerano et al.
Environmental science & technology, 45(2), 589-594 (2010-12-09)
Previous studies have shown environmentally persistent free radicals (EPFRs) form when chlorine- and hydroxy-substituted benzenes chemisorb on Cu(II)O-containing surfaces under postcombustion conditions. This paper reports the formation of EPFRs on silica particles containing 5% Fe(III)(2)O(3). The EPFRs are formed by
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