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12-Hydroxyabietic acid

12-Hydroxyabietic acid

Catalog No. BCN5284
Size Price Stock
20mg $298 In stock
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Quality Control of 12-Hydroxyabietic acid

Chemical structure

12-Hydroxyabietic acid

12-Hydroxyabietic acid Dilution Calculator

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12-Hydroxyabietic acid Molarity Calculator



Chemical Properties of 12-Hydroxyabietic acid

Cas No. 3484-61-5 SDF Download SDF
Chemical Name (1R,4aR,4bR,6S,10aR)-6-hydroxy-1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylic acid
Standard InChI InChI=1S/C20H30O3/c1-12(2)14-10-13-6-7-17-19(3,15(13)11-16(14)21)8-5-9-20(17,4)18(22)23/h6,10,12,15-17,21H,5,7-9,11H2,1-4H3,(H,22,23)/t15-,16-,17+,19+,20+/m0/s1
Type of Compound Diterpenoids Appearance Powder
Formula C20H30O3 M.Wt 318.5
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.
Shipping Condition Packaging according to customer requirements(5mg, 10mg, 20mg and more). Ship via FedEx, DHL, UPS, EMS or other courier with RT , or blue ice upon request.

Preparing Stock Solutions of 12-Hydroxyabietic acid

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 3.1397 mL 15.6986 mL 31.3972 mL 62.7943 mL 78.4929 mL
5 mM 0.6279 mL 3.1397 mL 6.2794 mL 12.5589 mL 15.6986 mL
10 mM 0.314 mL 1.5699 mL 3.1397 mL 6.2794 mL 7.8493 mL
50 mM 0.0628 mL 0.314 mL 0.6279 mL 1.2559 mL 1.5699 mL
100 mM 0.0314 mL 0.157 mL 0.314 mL 0.6279 mL 0.7849 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.

Preparation of 12-Hydroxyabietic acid

This product is isolated and purified from the barks of Pinus yunnanensis

References on 12-Hydroxyabietic acid

Isolation and identification of diterpenoids from Pinus koraiensis.[Pubmed: 18589751]

OBJECTIVE: To study chemical compounds from Pinus koraiensis. METHODS: The constituents were isolated by chromatographic method and the structures were identified on the basis of spectral alanlysis. RESULTS: Eight compounds were identified as 8 (14)-podocarpen-13-on-18-oic acid (1), 15-hydroxydehydroabietic acid (2), 12-Hydroxyabietic acid (3), lambertianic acid (4), dehydroabietic acid (5), sandaracopimaric acid (6), beta-sitosterol (7), daucosterol (8). CONCLUSION: Compounds 1--6 are isolated from this plant for the first time.


12-Hydroxyabietic acid ,3484-61-5,Nature Products, supplier, inhibitor,Antagonist,Blocker,Modulator,Agonist, activators, activates, potent, BioCrick

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