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2237-14-1

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2237-14-1 Usage

Description

1,4-BENZOQUINONE-D4, also known as p-benzoquinone, is a stable, heavy isotope-labeled derivative of the organic compound benzoquinone. It is commonly used in research and testing as a stable isotope-labeled internal standard for the determination and quantification of benzoquinone in various samples.
Used in Environmental Analysis:
1,4-BENZOQUINONE-D4 is used as an internal standard for the accurate and precise analysis of benzoquinone levels in environmental samples, such as air, water, and soil.
Used in Forensic Toxicology:
1,4-BENZOQUINONE-D4 is used as an internal standard for the identification and quantification of benzoquinone in biological samples, such as blood, urine, and tissue, in forensic investigations.
Used in Biochemical Studies:
1,4-BENZOQUINONE-D4 is used as an internal standard for the study of benzoquinone and its related compounds in biochemical research, including their roles in metabolic pathways and enzyme reactions.
Used in Analytical Testing:
1,4-BENZOQUINONE-D4 is used as an internal standard for the accurate and precise quantification of benzoquinone in various samples, ensuring reliable results in analytical testing.

Check Digit Verification of cas no

The CAS Registry Mumber 2237-14-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,3 and 7 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2237-14:
(6*2)+(5*2)+(4*3)+(3*7)+(2*1)+(1*4)=61
61 % 10 = 1
So 2237-14-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H4O2/c7-5-1-2-6(8)4-3-5/h1-4H/i1D,2D,3D,4D

2237-14-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3,5,6-tetradeuteriocyclohexa-2,5-diene-1,4-dione

1.2 Other means of identification

Product number -
Other names p-Benzoquinone-d4

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:2237-14-1 SDS

2237-14-1Relevant articles and documents

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Ogata et al.

, p. 2715,2720 (1969)

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Development of isotope-enriched phosphatidylinositol-4- And 5-phosphate cellular mass spectrometry probes

Joffrin, Amélie M.,Saunders, Alex M.,Barneda, David,Flemington, Vikki,Thompson, Amber L.,Sanganee, Hitesh J.,Conway, Stuart J.

, p. 2549 - 2557 (2021/03/01)

Synthetic phosphatidylinositol phosphate (PtdInsPn) derivatives play a pivotal role in broadening our understanding of PtdInsPnmetabolism. However, the development of such tools is reliant on efficient enantioselective and regioselective synthetic strategies. Here we report the development of a divergent synthetic route applicable to the synthesis of deuterated PtdIns4Pand PtdIns5Pderivatives. The synthetic strategy developed involves a key enzymatic desymmetrisation step using Lipozyme TL-IM. In addition, we optimised the large-scale synthesis of deuteratedmyo-inositol, allowing for the preparation of a series of saturated and unsaturated deuterated PtdIns4Pand PtdIns5Pderivatives. Experiments in MCF7 cells demonstrated that these deuterated probes enable quantification of the corresponding endogenous phospholipids in a cellular setting. Overall, these deuterated probes will be powerful tools to help improve our understanding of the role played by PtdInsPnin physiology and disease.

Reductive Dehalogenation and Ring Saturation of Halogenated Hydroquinones, Catechol, and Resorcinol with Raney Alloys in NaOD-D2O Solution Leading to Hydroquinones, 1,4-Cyclohexanediol and 1,3-Cyclohexanedione Labeled with Deuterium

Tsuzuki, Hirohisa,Iyama, Hironobu,Tsukinoki, Takehito,Mukumoto, Mamoru,Yonemitsu, Tadashi,et al.

, p. 1701 - 1716 (2007/10/02)

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