| English alias |
Bilobalide;(-)-bilobalide from ginkgo leaves;(-)-Bilobalide;(-)-Bilobalide from Ginkgo biloba leaves;(-)-Bilobalide, froM Ginkgo biloba;(?)-Bilobalide;(−)-Bilobalide;Bilobalide A;BILOBALIDE(AS);BILOBALIDE(P);BILOBALIDE(P) PrintBack;4H,5aH,9H-Furo[2,3-b]furo[3',2':2,3]cyclopenta[1,2-c]furan-2,4,7(3H,8H)-trione,9-(1,1-dimethylethyl)-10,10a-dihydro-8,9-dihydroxy-, [5aR-(3aS*,5aa,8b,8aS*,9a,10aa)]-;4H,5aH,9H-Furo[2,3-b]furo[3',2':2,3]cyclopenta[1,2-c]furan-2,4,7(3H,8H)-trione,9a-tert-butyl-10,10ab-dihydro-8a,9-dihydroxy-, (-)- (8CI);Bilobalid;[
""
];(?)-Bilobalide from Ginkgo biloba leaves |
| Content |
Bilobalide, CAS# 33570-04-6
Analysis method: HPLC 13cNMR、1HNMR、MS
Molecular formula: C15H18O8
Molecular weight: 326.29862
CAS No.: 33570-04-6
Apperance: White powder
Grade: 98%-99% （ HPLC ）
Packaging: As required.
Annual capacity: 25 kgs
Storage condition: Refrigerate and protect from light.
Plant source: 银杏叶/The leaves of Ginkgo biloba L.
Bilobalide A belongs to the class of organic compounds known as ginkgolides and bilobalides. These are diterpene lactones with a structure based either on the gingkolide or the bilobalide skeleton. The ginkgolide skeleton is a very rigid structure consisting of hexacyclic C20 trilactone. The cis-fused F/A/D/C ring junction forms an empty semi-ball hole, the D ring contains a cage form tetrahydrofuran ring which occupies the center of the empty hole, and the oxygen atoms of the D,C and F ring and 10-hydroxyl group consist of an analogous crown ether structure. Bilobalide A is an extremely weak basic (essentially neutral) compound (based on its pKa).
——Source: HMDB
Bilobalide is one of our superior products. Tauto Biotech successfully extracted 98%-99% （ HPLC ） Bilobalide by utilizing our own patented extraction method(HSCCC). Related technology is applicable to production lines with a scale of ≥25 kgs.
Advantages: continuous supply, strict QA, HSCCC technology, annual production capacity ≥25 kgs.
Related products
Ingredients found in 银杏叶/The leaves of Ginkgo biloba L.:
| RM-0011 |
Bilobalide |
33570-04-6 |
C15H18O8 |
326.29862 |
| RM-0007 |
Ginkgolide A |
15291-75-5 |
C20H24O9 |
408.39916 |
| RM-0008 |
Ginkgolide B |
15291-77-7 |
C20H24O10 |
424.39856 |
| RM-0009 |
Gingkolide C |
15291-76-6 |
C20H24O11 |
440.39796 |
| RM-0010 |
Ginkgolide J |
107438-79-9 |
C20H24O10 |
424.39856 |
| RM-0020 |
Ginkgolic Acid C15:0 |
16611-84-0 |
C22H36O3 |
348.53 |
| RM-0017 |
Ginkgolic Acid (C15:1) |
22910-60-7 |
C22H34O3 |
346.5076 |
| RM-0016 |
Ginkgolic Acid (C13:0) |
20261-38-5 |
C20H32O3 |
320.4698 |
| RM-0018 |
Ginkgolic Acid (C17:1) |
111047-30-4 |
C24H38O3 |
374.5612 |
|
A RM-0015
B RM-0954
|
Ginkgolic Acids
(C13:0,C15:1,C17:2,C15:0,C17:1)
|
/ |
/ |
|
| RM-0012 |
Isorhamnetin |
480-19-3 |
C16H12O7 |
316.26228 |
| RM-0013 |
Kaempferol |
520-18-3 |
C15H10O6 |
286.2363 |
|
