100683-54-3 Usage
Uses
Used in Research and Laboratory Settings:
MALONDIALDEHYDE TETRABUTYLAMMONIUM SALT is used as a lipid peroxidation marker for studying oxidative stress, inflammation, and various diseases. Its increased stability and solubility in aqueous solutions make it easier to measure and analyze in different experimental conditions.
Used in Pharmaceutical and Therapeutic Development:
MALONDIALDEHYDE TETRABUTYLAMMONIUM SALT is used as a research tool in the development of potential therapies and interventions targeting oxidative stress-related conditions and diseases. Its ability to serve as a marker for lipid peroxidation aids in understanding the mechanisms and pathways involved in these conditions, thereby contributing to the discovery of novel treatment options.
Used in Diagnostic Applications:
In the medical and diagnostic industry, MALONDIALDEHYDE TETRABUTYLAMMONIUM SALT is used as a biomarker for assessing oxidative stress levels in patients. Its stability and solubility properties make it suitable for use in diagnostic tests and assays, helping to identify and monitor the presence of oxidative stress in various disease conditions.
Used in Nutritional and Food Industry:
MALONDIALDEHYDE TETRABUTYLAMMONIUM SALT can be used in the nutritional and food industry as an indicator of lipid oxidation in food products. Its ability to measure lipid peroxidation can help in assessing the quality and shelf life of food items, ensuring their safety and nutritional value for consumers.
Check Digit Verification of cas no
The CAS Registry Mumber 100683-54-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,6,8 and 3 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 100683-54:
(8*1)+(7*0)+(6*0)+(5*6)+(4*8)+(3*3)+(2*5)+(1*4)=93
93 % 10 = 3
So 100683-54-3 is a valid CAS Registry Number.
InChI:InChI=1/C16H36N.C3H4O2/c1-5-9-13-17(14-10-6-2,15-11-7-3)16-12-8-4;4-2-1-3-5/h5-16H2,1-4H3;1-4H/q+1;/p-1/b;2-1+
100683-54-3Relevant academic research and scientific papers
Racemic and Enantiomeric all-trans-Fecapentaene-12 and -14.
Pfaendler, Hans Rudolf,Maier, Franz Karl,Klar, Sonja,Goeggelmann, Waltraud
, p. 449 - 454 (2007/10/02)
The syntheses of the following crystalline all-trans compounds are described: (+/-)-fecapentaene-12 (1a), natural (S)-(+)-fecapentaene-12, unnatural (R)-(-)-fecapentaene-12, (+/-)-fecapentaene-14 (1b), and (S)-(+)-fecapentaene-14.Both enantiomers and the
