p-Benzoquinone, reagent grade, ≥98% | C6H4(=O)2

Properties

Related Categories	B, Bioactive Small Molecules, Biochemicals and Reagents, Cell Biology, Enzyme Inhibitors, Enzyme Inhibitors by Enzyme, Enzymes, Inhibitors, and Substrates, Hordeum vulgare (Barley), Nutrition Research, Phytochemicals by Plant (Food/Spice/Herb), R to Z, Tyramine oxidase More...
grade	reagent grade
vapor density	3.73 (vs air)
vapor pressure	0.1 mmHg ( 25 °C)
assay	≥98%
autoignition temp.	815 °F
mp	113-115 °C(lit.)
Gene Information	human ... ACHE(43), BCHE(590), CES1(1066)

Description

General description

Free radical inhibitor

Packaging

1 kg in glass bottle

5, 100, 500 g in glass bottle

Application

Dienophile employed in Diels-Alder cycloadditions to form naphthoquinones,¹ and 1,4-phenanthrenediones.²

Price and Availability

Suggested Laboratory Gloves

This substance has been tested against several types of hand protection for CE compliance. Click below to find the recommended gloves for handling this product.

for splash & immersion protection

Related Papers

Identification and characterization of novel benzil (diphenylethane-1,2-dione) analogues as inhibitors of mammalian carboxylesterases. Randy M Wadkins et al J. Med. Chem. 48, 2906-15, (2005)

Documents

Certificate of Analysis

Certificate of Origin

Safety Information

Symbol	GHS06, GHS09
Signal word	Danger
Hazard statements	H301-H315-H319-H331-H335-H400
Precautionary statements	P261-P273-P301 + P310-P305 + P351 + P338-P311
Personal Protective Equipment	Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
Hazard Codes (Europe)	T,N
Risk Statements (Europe)	23/25-36/37/38-50
Safety Statements (Europe)	26-28-45-61
RIDADR	UN 2587 6.1/PG 2
WGK Germany	3
RTECS	DK2625000

Technical information & documentation associated with this product is available in the Safety & Documentation tab.

Papers

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1. Indian J. Chem. B 32, 1113, (1993)

2. J. Org. Chem. 59, 1889, (1994)

Identification and characterization of novel benzil (diphenylethane-1,2-dione) analogues as inhibitors of mammalian carboxylesterases. Randy M Wadkins et al J. Med. Chem. 48, 2906-15, (2005)

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Chemical genetics reveals a complex functional ground state of neural stem cells Diamandis, P., et. al. Nat. Chem. Biol. 3(5), 268-273, (2007)

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Indoleamine 2,3-dioxygenase is the anticancer target for a novel series of potent naphthoquinone-based inhibitors. Sanjeev Kumar et al J. Med. Chem. 51, 1706-18, (2008)

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Bioactivities of simplified adociaquinone B and naphthoquinone derivatives against Cdc25B, MKP-1, and MKP-3 phosphatases. Shugeng Cao et al Bioorg. Med. Chem. 17, 2276-81, (2009)

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Merck 14,8074

Beil. 7,IV,2065

Fieser 1,49 / Fieser 7,55

Aldrich MSDS 1, 164:A / Corp MSDS 1 (1), 367:A / FT-NMR 1 (1), 713:A / IR-Spectra (3), 268:A / IR-Spectra (2), 239:D / NMR-Reference 2 (1), 414:C / RegBook 1 (1), 491:M / Sax 6, 388 / Sigma FT-IR 1 (2), 309:A / Structure Index 1, 70:B:8