Lutein monopalmitateCAS# 115182-29-1 |
Quality Control & MSDS
Number of papers citing our products
Chemical structure
Cas No. | 115182-29-1 | SDF | Download SDF |
PubChem ID | N/A | Appearance | Powder |
Formula | C56H86O3 | M.Wt | 807.3 |
Type of Compound | Terpenoids | Storage | Desiccate at -20°C |
Solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | ||
General tips | For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20℃ for several months. We recommend that you prepare and use the solution on the same day. However, if the test schedule requires, the stock solutions can be prepared in advance, and the stock solution must be sealed and stored below -20℃. In general, the stock solution can be kept for several months. Before use, we recommend that you leave the vial at room temperature for at least an hour before opening it. |
||
About Packaging | 1. The packaging of the product may be reversed during transportation, cause the high purity compounds to adhere to the neck or cap of the vial.Take the vail out of its packaging and shake gently until the compounds fall to the bottom of the vial. 2. For liquid products, please centrifuge at 500xg to gather the liquid to the bottom of the vial. 3. Try to avoid loss or contamination during the experiment. |
||
Shipping Condition | Packaging according to customer requirements(5mg, 10mg, 20mg and more). Ship via FedEx, DHL, UPS, EMS or other couriers with RT, or blue ice upon request. |
Lutein monopalmitate Dilution Calculator
Lutein monopalmitate Molarity Calculator
1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
1 mM | 1.2387 mL | 6.1935 mL | 12.387 mL | 24.7739 mL | 30.9674 mL |
5 mM | 0.2477 mL | 1.2387 mL | 2.4774 mL | 4.9548 mL | 6.1935 mL |
10 mM | 0.1239 mL | 0.6193 mL | 1.2387 mL | 2.4774 mL | 3.0967 mL |
50 mM | 0.0248 mL | 0.1239 mL | 0.2477 mL | 0.4955 mL | 0.6193 mL |
100 mM | 0.0124 mL | 0.0619 mL | 0.1239 mL | 0.2477 mL | 0.3097 mL |
* Note: If you are in the process of experiment, it's necessary to make the dilution ratios of the samples. The dilution data above is only for reference. Normally, it's can get a better solubility within lower of Concentrations. |
Calcutta University
University of Minnesota
University of Maryland School of Medicine
University of Illinois at Chicago
The Ohio State University
University of Zurich
Harvard University
Colorado State University
Auburn University
Yale University
Worcester Polytechnic Institute
Washington State University
Stanford University
University of Leipzig
Universidade da Beira Interior
The Institute of Cancer Research
Heidelberg University
University of Amsterdam
University of Auckland
TsingHua University
The University of Michigan
Miami University
DRURY University
Jilin University
Fudan University
Wuhan University
Sun Yat-sen University
Universite de Paris
Deemed University
Auckland University
The University of Tokyo
Korea University
- Lutein monostearate
Catalog No.:BCX1560
CAS No.:115156-87-1
- Lutein laurate-myristate
Catalog No.:BCX1559
CAS No.:117116-36-6
- 5-Methyl-5H-furan-2-one
Catalog No.:BCX1558
CAS No.:591-11-7
- Pantolactone
Catalog No.:BCX1557
CAS No.:599-04-2
- cis-Myrislignan
Catalog No.:BCX1556
CAS No.:52190-21-3
- Docosahexaenoic acid
Catalog No.:BCX1555
CAS No.:6217-54-5
- Delavinone
Catalog No.:BCX1554
CAS No.:96997-98-7
- Yubeinine
Catalog No.:BCX1553
CAS No.:157478-01-8
- Ebeiedinone
Catalog No.:BCX1552
CAS No.:25650-68-4
- Sibiricaxanthone A
Catalog No.:BCX1551
CAS No.:241125-76-8
- Dihydrolapachenole
Catalog No.:BCX1550
CAS No.:20213-26-7
- Lactiflorin
Catalog No.:BCX1549
CAS No.:1361049-59-3
- Lutein palmitate stearate
Catalog No.:BCX1562
CAS No.:79313-82-9
- Lutein monomyristate
Catalog No.:BCX1563
CAS No.:56842-49-0
- Lutein dimyristate
Catalog No.:BCX1564
CAS No.:86853-02-3
- Lutein myristate palmitate
Catalog No.:BCX1565
CAS No.:104784-49-8
- Lutein distearate
Catalog No.:BCX1566
CAS No.:86852-15-5
- Pinocembrin 7-O-[4'',6''-hexahydroxydiphenoyl]-β-D-glucoside
Catalog No.:BCX1567
CAS No.:205370-58-7
- 18α-Glycyrrhetinic acid Monoglucuronide
Catalog No.:BCX1568
CAS No.:400870-85-1
- α-Sanshool
Catalog No.:BCX1569
CAS No.:504-97-2
- Escin Ie
Catalog No.:BCX1570
CAS No.:1613506-26-5
- Trisodium UDP-glucuronic acid
Catalog No.:BCX1571
CAS No.:63700-19-6
- Uridine diphosphate rhamnose
Catalog No.:BCX1572
CAS No.:1955-26-6
- Uridine diphosphate xylose
Catalog No.:BCX1573
CAS No.:3616-06-6
Lutein ester in serum after lutein supplementation in human subjects.[Pubmed:9924266]
Br J Nutr. 1998 Nov;80(5):445-9.
Lutein, one of the major carotenoids present in serum, is also widely consumed by most populations. For the purpose of testing the potential health benefits of several carotenoids, lutein was supplied as part of an intervention trial to test whether the consumption of these food constituents reduces oxidative damage to human tissue components. Lutein from a natural source (15 mg/d as mixed ester forms) was supplied for 4 months to eighteen non-smoking, apparently healthy volunteers (nine men, nine women) aged 25-45 years. The serum carotenoid profile was analysed at baseline and monthly thereafter. On average, lutein concentrations increased 5-fold after the first month of supplementation (mean 1.34 (range 0.6-3.34) mumol/l). On reviewing the results, in those volunteers whose lutein levels surpassed 1.05 mumol/l (fourteen of seventeen), we tentatively identified Lutein monopalmitate along with another unidentified ester (possibly from a monoketocarotenoid) in serum. Lutein levels returned to baseline values and ester forms were not present 3 months after supplementation was discontinued. Their concentrations did not correlate with, and represented less than 3% of, lutein levels achieved in serum. They were observed before development of, and despite the presence of, carotenodermia. To our knowledge, this is the first time xanthophyll esters have been described in human serum. In view of the fact that xanthophyll esters have not been previously reported in serum and chylomicrons, it seems unlikely that these ester forms would be a reflection of the contents of the capsule. They may indicate a 'ceiling effect' on or saturation of the transport capacity for xanthophylls, and may have been re-esterified in vivo because of the unusual dietary conditions. The determination of the physiological importance of this finding will require further investigation, although neither haematological nor biochemical changes were detected.