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12-Hydroxyabietic acid

CAS# 3484-61-5

12-Hydroxyabietic acid

Catalog No. BCN5284----Order now to get a substantial discount!

Product Name & Size Price Stock
12-Hydroxyabietic acid:5mg Please Inquire In Stock
12-Hydroxyabietic acid:10mg Please Inquire In Stock
12-Hydroxyabietic acid:20mg Please Inquire In Stock
12-Hydroxyabietic acid:50mg Please Inquire In Stock

Quality Control of 12-Hydroxyabietic acid

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Chemical structure

12-Hydroxyabietic acid

3D structure

Chemical Properties of 12-Hydroxyabietic acid

Cas No. 3484-61-5 SDF Download SDF
PubChem ID 52325853 Appearance Powder
Formula C20H30O3 M.Wt 318.5
Type of Compound Diterpenoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
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
SMILES CC(C)C1=CC2=CCC3C(C2CC1O)(CCCC3(C)C(=O)O)C
Standard InChIKey DYNISIGUMYFVJW-OCBLOMHFSA-N
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.

Source of 12-Hydroxyabietic acid

The barks of Pinus yunnanensis

Protocol of 12-Hydroxyabietic acid

Structure Identification
Zhong Yao Cai. 2008 Jan;31(1):53-5.

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

To study chemical compounds from Pinus koraiensis.
METHODS AND RESULTS:
The constituents were isolated by chromatographic method and the structures were identified on the basis of spectral alanlysis. 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).
CONCLUSIONS:
Compounds 1--6 are isolated from this plant for the first time.

12-Hydroxyabietic acid Dilution Calculator

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12-Hydroxyabietic acid Molarity Calculator

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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.

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References on 12-Hydroxyabietic acid

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

Zhong Yao Cai. 2008 Jan;31(1):53-5.

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.

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