Chemodex

o-Dianisidine

CHF 81.00
In stock
CDX-D1023-G01010 gCHF 81.00
CDX-D1023-G05050 gCHF 326.00
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Product Details
Synonyms 3,3´-Dimethoxybenzidine; Fast Blue B; Dianisidine; Acetamine diazo black RD; CI Disperse black 6; Cibacete diazo navy blue 2B; Diato blue base B
Product Type Chemical
Properties
Formula

C14H16N2O2

MW 244.29
CAS 119-90-4
RTECS DD0875000
Purity Chemicals ≥97.0% (GC)
Appearance Light yellow to brown to pink powder.
Solubility Soluble in methanol (10 mg/ml) or ethanol (10 mg/ml).
Declaration Manufactured by Chemodex.
Other Product Data

Click here for Original Manufacturer Product Datasheet
Our product description may differ slightly from the original manufacturers product datasheet.

InChi Key JRBJSXQPQWSCCF-UHFFFAOYSA-N
Smiles NC1=C(OC)C=C(C2=CC(OC)=C(N)C=C2)C=C1
Shipping and Handling
Shipping AMBIENT
Short Term Storage +20°C
Long Term Storage +4°C
Handling Advice Protect from light and moisture.
Use/Stability Stable for at least 2 years after receipt when stored at RT.
Documents
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Product Specification Sheet
Datasheet Download PDF
Description

o-Dianisidine is a peroxidase substrate and used as a redox indicator dye. Redox indicators are colorimetric reagents which provide a characteristic color change at a specific electrode potential. o-Dianisidine has been used for neutrophil myeloperoxidase activity (MPO) assay or measurment of glucose-oxidase or caeruloplasmin oxidase. It is used as an intermediate for the preparation of azo dyes, pigments and o-dianisidine diisocyanate, which finds application in adhesives, polyurethane elastomers and resins. It is also used in various industries like leather, paper, plastics, rubber and textiles. It acts as a reagent to detect metals, thiocyanates and nitrites. It is incompatible with strong oxidizing agents.

Product References

(1) A.S. Hugget & D.A. Nixon; Lancet 273, 368 (1957) | (2) K.H. Schosinsky, et al.; Clin. Chem. 20, 1556 (1974) | (3) A. Hulanicki & S. Glab; Pure Appl. Chem. 50, 463 (1978) | (4) K. Takayama & M. Miura; Jpn. J. Physiol. 31, 269 (1981) | (5) W.F. Beyer & I. Fridovich; Anal. Biochem. 170, 512 (1988) | (6) K. Hunger, et al.; Ullmann's Encycl. Industr. Chem. (2000) | (7) M. Catala Icardo, et al.; Analyst 126, 2087 (2001) | (8) J. Jasnowska, et al.; Bioelectrochemistry 64, 85 (2004) | (9) E. Perju, et al.; Liq. Cryst. 42, 1309 (2015) | (10) S. Sundaram, et al.; RSC Adv. 5, 45996 (2015)

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