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15-HYDROXY-7-OXODEHYDROABIETICACID is a natural organic compound belonging to the class of diterpenoids, which are derived from the isoprene unit. Found in several plant species, this chemical has garnered interest in pharmaceutical and medicinal research due to its potential anti-inflammatory, antioxidant, and antiproliferative properties. It has also been studied for its ability to protect cells from oxidative stress and reduce inflammation, as well as its potential in inhibiting cancer cell growth, making it a promising candidate for further exploration in various fields, including medicine and pharmaceuticals.

95416-25-4

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95416-25-4 Usage

Uses

Used in Pharmaceutical Research:
15-HYDROXY-7-OXODEHYDROABIETICACID is used as a subject of interest in pharmaceutical research for its potential anti-inflammatory, antioxidant, and antiproliferative properties. Its ability to protect cells from oxidative stress and reduce inflammation makes it a valuable compound for the development of new medications.
Used in Cancer Treatment:
In the field of oncology, 15-HYDROXY-7-OXODEHYDROABIETICACID is used as a promising candidate for cancer treatment due to its potential in inhibiting the growth of cancer cells. Further exploration and research are needed to harness its potential in developing novel therapeutic agents for various types of cancer.
Used in Antioxidant Formulations:
15-HYDROXY-7-OXODEHYDROABIETICACID is used as an antioxidant in various formulations, leveraging its ability to protect cells from oxidative stress. This application can be beneficial in the development of health supplements, skincare products, and other consumer goods that aim to promote overall health and well-being.
Used in Anti-Inflammatory Applications:
In the medical field, 15-HYDROXY-7-OXODEHYDROABIETICACID is used as an anti-inflammatory agent, targeting conditions and diseases characterized by inflammation. Its potential to reduce inflammation can contribute to the development of new treatments for inflammatory disorders.
Used in Medicinal Research:
15-HYDROXY-7-OXODEHYDROABIETICACID is utilized in medicinal research to explore its wide range of bioactivities and potential applications in medicine. 15-HYDROXY-7-OXODEHYDROABIETICACID's diverse properties make it a valuable asset for investigating new therapeutic approaches and advancing the understanding of various health conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 95416-25-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,4,1 and 6 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 95416-25:
(7*9)+(6*5)+(5*4)+(4*1)+(3*6)+(2*2)+(1*5)=144
144 % 10 = 4
So 95416-25-4 is a valid CAS Registry Number.

95416-25-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 15-Hydroxy-7-oxoabieta-8,11,13-trien-18-oic acid

1.2 Other means of identification

Product number -
Other names Tetrahydroabietyl alcohol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:95416-25-4 SDS

95416-25-4Relevant academic research and scientific papers

Aerobic oxidation of 8,11,13-abietatrienes catalyzed by N-hydroxyphthalimide combined with 2,2′-azobis(4-methoxy-2,4-dimethylvaleronitrile) and its application to synthesis of naturally occurring diterpenes

Matsushita, Yoh-ichi,Sugamoto, Kazuhiro,Iwakiri, Yoshihisa,Yoshida, Satoru,Chaen, Takehito,Matsui, Takanao

scheme or table, p. 3931 - 3934 (2010/08/07)

Methyl 8,11,13-abietatriene-18-oate (1b) and 7-oxo-8,11,13-abietatrienes 10 and 15 were converted into 15-hydroperoxy-7-oxo-8,11,13-abietatrienes 13 and 16 by aerobic oxidation catalyzed by N-hydroxyphthalimide (NHPI) combined with 2,2′-azobis(4-methoxy-2

Microbial transformations of diterpene acids

Vorob'ev,Grishko,Ivshina,Shmidt,Pokrovskii,Kuyukina,Tolstikov

, p. 72 - 73 (2007/10/03)

The ability of Rhodococcus bacteria to transform dehydroabietic and isopimaric acids with a high degree of conversion (up to 95%) was detected.

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