2,3-Dichloro-5,6-dicyano-1,4-benzoquinone (DDQ)

Cat# B2015288

Size : 10g

Marca : Molecular Depot

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2,3-Dichloro-5,6-dicyano-1,4-benzoquinone (DDQ)

Catalog Number: B2015288 (10 g)
2,3-Dichloro-5,6-dicyano-1,4-benzoquinone (DDQ) is a high quality 2,3-Dichloro-5,6-dicyano-1,4-benzoquinone (DDQ). This product has been used as a molecular tool for various biochemical applications. It has also been used in a wide array of other chemical and immunological applications. Custom bulk amounts of this product are available upon request.

Live enquiry about this product via Text/SMS: 1-858-900-3210.

SKU: B2015288 Categories: Cell Biology, Chemicals Tag: MD 1000

Product Description

5/5 - (1 vote)

2,3-Dichloro-5,6-dicyano-1,4-benzoquinone (DDQ)
Catalog number: B2015288
Lot number: Batch Dependent
Expiration Date: Batch dependent
Amount: 10 g
Molecular Weight or Concentration: 227.01 g/mol
Supplied as: Powder
Applications: a molecular tool for various biochemical applications
Storage: RT
Keywords: 4,5-Dichloro-3,6-dioxo-1,4-cyclohexadiene-1,2-dicarbonitrile, DDQ
Grade: Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity >18 MΩ-cm) and are filtered through 0.22 um.

References:
1: Aljaber KA, Darwish IA, Al-Hossaini AM. Spectrophotometric Study of Charge-Transfer Complexes of Ruxolitinib with Chloranilic Acid and 2,3-Dichloro-5,6-dicyano-1,4-benzoquinone: An Application to the Development of a Green and High-Throughput Microwell Method for Quantification of Ruxolitinib in Its Pharmaceutical Formulations Molecules. 2023 Nov 30;28(23):7877.
2: Mostafa GAE, Yousef TA, ElGamal AA, Homoda AMA, AlRabiah H. Tamoxifen charge transfer complexes with 2,3-dichloro-5,6-dicyano-1,4-benzoquinone and 7,7,8,8-tetracyanoquinodimethan: Synthesis, spectroscopic characterization and theoretical study Bioorg Chem. 2022 Mar;120:105603.
3: Bakheit AH, Al-Salahi R, Al-Majed AA. Thermodynamic and Computational (DFT) Study of Non-Covalent Interaction Mechanisms of Charge Transfer Complex of Linagliptin with 2,3-Dichloro-5,6-dicyano-1,4-benzoquinone (DDQ) and Chloranilic acid (CHA) Molecules. 2022 Sep 25;27(19):6320.
4: Zhang Y, Zhang F, Ma K, Tang G. Experimental and DFT studies on the vibrational and electronic spectra of 2,3-dichloro-5,6-dicyano-1,4-benzoquinone Spectrochim Acta A Mol Biomol Spectrosc. 2013 Mar 15;105:352-8.
5: Xia Q, Yang Y, Liu M. Spectrofluorimetric determination of fluoroquinolones in honey with 2,3-dichloro-5,6-dicyano-1,4-benzoquinone in the presence of β-cyclodextrin J Fluoresc. 2013 Jul;23(4):713-23.
6: Zhang W, Ma H, Zhou L, Sun Z, Du Z, Miao H, Xu J. Organocatalytic oxidative dehydrogenation of dihydroarenes by dioxygen using 2,3-dichloro-5,6-dicyano-benzoquinone (DDQ) and NaNO2 Molecules. 2008 Dec 18;13(12):3236-45.
7: Mostafa GAE, Bakheit A, AlMasoud N, AlRabiah H. Charge Transfer Complexes of Ketotifen with 2,3-Dichloro-5,6-dicyano-p-benzoquinone and 7,7,8,8-Tetracyanoquodimethane: Spectroscopic Characterization Studies Molecules. 2021 Apr 2;26(7):2039.
8: Lloyd D, Bylsma M, Bright DK, Chen X, Bennett CS. Mild Method for 2-Naphthylmethyl Ether Protecting Group Removal Using a Combination of 2,3-Dichloro-5,6-dicyano-1,4-benzoquinone (DDQ) and β-Pinene J Org Chem. 2017 Apr 7;82(7):3926-3934.
9: Ganesh K, Balraj C, Satheshkumar A, Elango KP. Spectroscopic investigation on the mechanism of formation of molecular complexes of albendazole and trimethoprim with 2,3-dichloro-5,6-dicyano-1,4-benzoquinone Spectrochim Acta A Mol Biomol Spectrosc. 2012 Jun 15;92:46-55.
10: Ganesh K, Balraj C, Elango KP. Spectroscopic and spectrofluorimetric studies on the interaction of irbesartan with 2,3-dichloro-5,6-dicyano-1,4-benzoquinone and iodine Spectrochim Acta A Mol Biomol Spectrosc. 2011 Sep;79(5):1621-9.

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Additional Information

Weight 2.6 oz
Dimensions 3.3 × 1.2 × 1.2 in