1-Triacontanol - CAS 593-50-0

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Category
Main Product
Product Name
1-Triacontanol
Catalog Number
593-50-0
Synonyms
triacontan-1-ol; 1-Triacontanol; Triacontan-1-ol; Melissylalcohol; Myricylalcohol; Triacontanol
CAS Number
593-50-0
Molecular Weight
438.81268;g/mol
Molecular Formula
C30H62O
Quantity
Data not available, please inquire.
COA
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MSDS
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Canonical SMILES
CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO
InChI
InChI=1S/C30H62O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-24-25-26-27-28-29-30-31/h31H,2-30H2,1H3
InChIKey
REZQBEBOWJAQKS-UHFFFAOYSA-N
Structure
CAS 593-50-0 1-Triacontanol
Specification
Purity
95%
Boiling Point
443.3ºC at 760 mmHg
Melting Point
86-87ºC
Density
0.841 g/cm3
Appearance
Granular or plate, white to off-white powder
Storage
2-8ºC
Related Products
Reference Reading
1.Investigation on pharmacokinetics, tissue distribution and excretion of 1-triacontanol in rats by gas chromatography-tandem mass spectrometry (GC-MS/MS).
Wang C1, Fan A, Deng S, Gao W, Zhang W, Yang W, Zhu X, Lu Y, Chen X. Xenobiotica. 2015 Jan;45(1):71-8. doi: 10.3109/00498254.2014.943334. Epub 2014 Jul 31.
1. 1-Triacontanol (TA) recently shows promising anti-tumor activity. The present study was aimed to develop a sensitive gas chromatography-tandem mass spectrometry method to explore the pharmacokinetic profiles, distribution and excretion of TA in Sprague-Dawley rats after oral administration of TA. Chromatography separation was performed on a HP-5MS column. 1-Octacosanal was used as the internal standard (IS). Quantification of TA and IS was carried out at m/z 495.6 → 97.0 and m/z 467.5 → 97.0, respectively, in positive electron ionization and multiple reaction monitoring mode. The pharmacokinetic parameters were calculated by non-compartmental analysis. 2. The area under concentration-time curve AUC0-6 h and AUC0-∞ for TA at 60 mg/kg were 87.737 ± 13.574 and 93.617 ± 17.62, respectively. The mean residence time was 3.25 ± 0.17 h. In addition, the elimination half-lives (t1/2) were (2.37 ± 1.23, 1.27 ± 0.49, 2.07 ± 0.93) h after single oral administration of 30, 60 and 120 mg/kg of TA.
2.Trace quantification of 1-triacontanol in beagle plasma by GC-MS/MS and its application to a pharmacokinetic study.
Wang C1, Fan A, Zhu X, Lu Y, Deng S, Gao W, Zhang W, Liu Q, Chen X. Biomed Chromatogr. 2015 May;29(5):749-55. doi: 10.1002/bmc.3351. Epub 2014 Oct 21.
1-Triacontanol (TA), a member of long chain fatty alcohol, has recently been received great attention owing to its antitumor activity. In this study, an accurate, sensitive and selective gas chromatography-tandem mass spectrometry method was developed and validated for the quantification of TA in beagle plasma using 1-octacosanal as the internal standard (IS) for the first time. With temperature programming, chromatographic separation was carried out on an HP-5MS column, using helium as carrier gas and argon as collision gas, both at a flow rate of 1 mL/min. TA was analyzed using positive ion electrospray ionization in multiple-reaction monitoring mode, with the precursor to product ion transitions of m/z 495.6 → 97.0 and m/z 467.5 → 97.0 for TA and the IS, respectively. The lower limit of quantitation, linearity, intra- and interday precision, accuracy, stability, extraction recovery and matrix effect of TA were within the acceptable limits.
3.The influence of 1-triacontanol on the growth, flowering, and quality of potted Bougainvillea plants (Bougainvillea glabra var. "Elizabeth Angus") under natural conditions.
Khandaker MM1, Faruq G, Rahman MM, Sofian-Azirun M, Boyce AN. ScientificWorldJournal. 2013 Jul 17;2013:308651. doi: 10.1155/2013/308651. eCollection 2013.
Selected physiological and biochemical parameters were monitored at the vegetative and reproductive growth stages in potted Bougainvillea plants treated with five different concentrations of TRIA. Advanced flowering, flower bud number, and blooming rate increased significantly with 0.5 and 1.0 mg/L TRIA treatments. Similarly, photosynthetic rate, pigment content, quantum yield, and stomatal conductance increased significantly with 2.5, 1.0, and 5.0 mg/L TRIA treatments. Higher levels of N, P, and K, as well as increased total soluble solids (TSS) and higher sugar and protein contents, were recorded in treated plants. Furthermore, 46% more flowers, a 1.5-fold increase in bract weight, increased longevity, and 40% less leaf abscission were recorded following 2.5 mg/L TRIA treatment. Phenol and flavonoid contents, sucrose phosphate synthase (SPS), and antioxidant activities were also markedly increased with 2.5 and 1.0 mg/L TRIA treatments.
4.1-Triacontanol cerotate; isolated from Marsilea quadrifolia Linn. ameliorates reactive oxidative damage in the frontal cortex and hippocampus of chronic epileptic rats.
Snehunsu A1, Ghosal C2, Kandwal M1, Yadav PK2, Nayak BS3, Rao KR1, Kamath SU2, Sahoo P4, Srinivasan KK5, Naduvil Narayanan S6, Kumar S1, Joseph A7. J Ethnopharmacol. 2015 Aug 22;172:80-4. doi: 10.1016/j.jep.2015.06.020. Epub 2015 Jun 24.
ETHNOPHARMACOLOGICAL RELEVANCE: Marsilea quadrifolia Linn. (MQ) has been used for insomnia and epileptic disorders in traditional Indian medicine. The present study is to isolate the active component responsible for antiepileptic property of MQ by evaluating its ability to minimize the reactive oxidative damage in brain due to chronic epilepsy in rat.
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