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15(S)-HETE SOLUTION, also known as (±)15-HETE, is one of the six monohydroxy fatty acids produced by the non-enzymatic oxidation of arachidonic acid. It exhibits biological activity similar to its constituent enantiomers. The 15(S)-HETE MaxSpec standard is a quantitative grade standard specifically prepared for mass spectrometry and related applications where quantitative reproducibility is essential. This solution is provided in a deactivated glass ampule sealed under argon, with its concentration verified by comparison to an independently prepared calibration standard. The product is guaranteed to meet identity, purity, stability, and concentration specifications, and it comes with a batch-specific certificate of analysis. Ongoing stability testing ensures the concentration remains accurate throughout the shelf life of the product. It is crucial to accurately measure volumes for the preparation of calibration standards and follow recommended storage and handling conditions to maintain product quality.

71030-36-9

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71030-36-9 Usage

Uses

Used in Mass Spectrometry Applications:
15(S)-HETE SOLUTION is used as a quantitative grade standard for mass spectrometry, ensuring accurate and reproducible results in various analytical procedures. Its high purity and guaranteed specifications make it a reliable choice for researchers and analysts.
Used in Research and Development:
In the field of research and development, 15(S)-HETE SOLUTION serves as an essential tool for studying the biological activity and properties of monohydroxy fatty acids. It aids scientists in understanding the role of these compounds in various biological processes and their potential applications in medicine and other industries.
Used in Quality Control and Assurance:
15(S)-HETE SOLUTION is utilized in quality control and assurance processes to verify the performance of analytical instruments and methods. Its guaranteed specifications and ongoing stability testing make it a suitable reference material for validating and calibrating mass spectrometry equipment and techniques.
Used in Pharmaceutical and Biomedical Industries:
The 15(S)-HETE SOLUTION can be employed in the pharmaceutical and biomedical industries for drug discovery, development, and testing. Its well-defined properties and high purity make it a valuable compound for investigating the effects of monohydroxy fatty acids on various diseases and conditions, potentially leading to the development of new therapeutic agents.
Used in Academic and Educational Settings:
In academic and educational institutions, 15(S)-HETE SOLUTION can be used as a teaching aid to help students understand the principles of mass spectrometry, analytical chemistry, and the role of bioactive compounds in biological systems. Its guaranteed specifications and stability make it an ideal material for laboratory experiments and demonstrations.

Check Digit Verification of cas no

The CAS Registry Mumber 71030-36-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,0,3 and 0 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 71030-36:
(7*7)+(6*1)+(5*0)+(4*3)+(3*0)+(2*3)+(1*6)=79
79 % 10 = 9
So 71030-36-9 is a valid CAS Registry Number.

71030-36-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (+/-)-15-HETE

1.2 Other means of identification

Product number -
Other names 15(S)-HETE

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:71030-36-9 SDS

71030-36-9Relevant academic research and scientific papers

Repurposing Resveratrol and Fluconazole to Modulate Human Cytochrome P450-Mediated Arachidonic Acid Metabolism

El-Sherbeni, Ahmed A.,El-Kadi, Ayman O. S.

, p. 1278 - 1288 (2016/04/26)

Cytochrome P450 (P450) enzymes metabolize arachidonic acid (AA) to several biologically active epoxyeicosatrienoic acids (EETs) and hydroxyeicosatetraenoic acids (HETEs). Repurposing clinically-approved drugs could provide safe and readily available means

Controlled formation of mono- and dihydroxy-resolvins from EPA and DHA using soybean 15-lipoxygenase

Dobson, Eleanor P.,Barrow, Colin J.,Kralovec, Jaroslav A.,Adcock, Jacqui L.

, p. 1439 - 1447 (2013/06/26)

Resolvins and protectins are important anti-infl ammatory and pro-resolution compounds derived from the enzymatic oxidation of omega-3 fatty acids all -cis -5,8,11,14,17- eicosapentaenoic acid (EPA) and all -cis -4,7,10,13,16,19-docosahexaenoic acid (DHA). We have developed a simple, controlled method to synthesize an array of resolvin and protectin analogs from fatty acid starting materials using soybean 15-lipoxygenase. The conditions were optimized for the production of both mono- and dihydroxy derivatives, with enzyme concentration and pH found to have a signifi cant effect on the reaction products. The methods were applied to fi ve biologically important omega-3 and omega-6 fatty acid substrates. Mono- and dihydroxy compounds were successfully synthesized from all substrates and the products were characterized by normal phase (NP) HPLC , GC-MS, TOF-MS, UV-visible (UV-vis) spectroscopy, and NMR spectroscopy. The methods could be further applied to any polyunsaturated fatty acids containing the cis -1,4,7,10-undecatetraene moiety to produce a range of novel compounds with potential biological activity. Copyright

Synthesis of phospholipids bearing a conjugated oxo-polyunsaturated fatty acid residue

Zhu, Changjin,Ohashi, Takaaki,Morimoto, Tatsuya,Onyango, Arnold N.,Takao, Kaneko,Shimizu, Sakayu,Nakajima, Shuhei,Baba, Naomichi

, p. 500 - 501 (2007/10/03)

2-(15'-Oxo-5',8',11',13'-eicosatetraenoyl)-1-stearoyl- sn- glycerol(3)phosphocholine (APC-CO) 1 and 2 and 2-(13'-oxo-9',11'- octadecadienoyl)-1-stearoyl-sn-glycero(3)phosphocholine (LPC-CO) 3 are synthesized and an analytical system established for the determination of geometrical isomers at the 13' position of APC-CO.

ISOMERIZATION OF EPOXIDES TO ALLYLIC ALCOHOLS USING METHYLMAGNESIUM N-CYCLOHEXYLISOPROPYLAMIDE

Mosset, Paul,Manna, Sukumar,Viala, Jacques,Falck, J.R.

, p. 299 - 302 (2007/10/02)

The scope of methylmagnesium N-cyclohexylisopropylamide promoted isomerizations of epoxides to allylic alcohols is described.

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