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612510

Sigma-Aldrich

1,2-Dichlorobenzene solution

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:
95-50-1
Molecular Weight:
147.00
MDL number:
MFCD00000535
UNSPSC Code:
12190000
PubChem Substance ID:
24882102
NACRES:
NA.12

grade

NMR reference standard

concentration

5% in acetone-d6 (99.9 atom % D)

technique(s)

NMR: suitable

NMR tube size

5 mm × 8 in.

SMILES string

Clc1ccccc1Cl

InChI

1S/C6H4Cl2/c7-5-3-1-2-4-6(5)8/h1-4H

InChI key

RFFLAFLAYFXFSW-UHFFFAOYSA-N

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Features and Benefits

1H resolution

Quantity

5 mm O.D. tube contains 0.700 mL.

Signal Word

Danger

Hazard Statements

H225,H317,H319,H336,H411

Hazard Classifications

Aquatic Chronic 2 - Eye Irrit. 2 - Flam. Liq. 2 - Skin Sens. 1 - STOT SE 3

Target Organs

Central nervous system

Supplementary Hazards

EUH066

Storage Class Code

3 - Flammable liquids

WGK

WGK 2

Flash Point(F)

1.4 °F - closed cup

Flash Point(C)

-17 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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1,2-Dichlorobenzene suitable for HPLC, 99%

Sigma-Aldrich

270598

1,2-Dichlorobenzene

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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