OLEANOLIC ACID METHYL ESTER - Names and Identifiers
Name | Methyl oleanolate
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Synonyms | Methyl oleanolate OLEANOLIC ACID METHYL ESTER OLEANOLIC ACID METHYLESTER WITH HPLC methyl (3beta)-3-hydroxyolean-12-en-28-oate 3β-Hydroxyolean-12-en-28-oic acid methyl ester 3-Hydroxy-(3β)-olean-12-en-28-oic acid methyl ester (3beta)-3-Hydroxy-olean-12-en-28-oic acid methyl ester methyl (4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate (4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid methyl ester
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CAS | 1724-17-0
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EINECS | 217-029-1 |
OLEANOLIC ACID METHYL ESTER - Physico-chemical Properties
Molecular Formula | C31H50O3
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Molar Mass | 470.73 |
Density | 1.07±0.1 g/cm3(Predicted) |
Melting Point | 200-205°C |
Boling Point | 526.1±50.0 °C(Predicted) |
pKa | 15.15±0.70(Predicted) |
Storage Condition | 2-8℃ |
MDL | MFCD00017382 |
OLEANOLIC ACID METHYL ESTER - Risk and Safety
Risk Codes | 36/37/38 - Irritating to eyes, respiratory system and skin.
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Safety Description | S22 - Do not breathe dust.
S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection.
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OLEANOLIC ACID METHYL ESTER - Introduction
Methyl oleanolate is a natural compound that belongs to the family of terpenoids. It is prepared by esterification of Methyl oleanate.
Methyl oleanolate is a colorless to light yellow crystalline solid with an aromatic odor. It is insoluble in water at room temperature, but soluble in some organic solvents such as ethanol and acetone. It has strong antioxidant properties, can inhibit many free radical reactions, and has anti-inflammatory, anti-tumor, analgesic and other biological activities.
In the field of medicine, Methyl oleanolate is widely used in the research and development of anti-tumor drugs. It has strong anti-tumor activity and can inhibit the proliferation and invasion of tumor cells. In addition, it is also used in the research and development of anti-inflammatory drugs, which can reduce inflammation and pain.
Methods for preparing Methyl oleanolate include extraction from plants or chemical synthesis. Methods of extraction from plants are relatively common, and one of the most commonly used methods is extraction from olive leaves. In terms of chemical synthesis, it is usually prepared by esterification using methyl olarate and cuprous bromide as starting materials.
Regarding safety information, Methyl oleanolate is generally considered to be relatively safe under normal conditions of use. However, it is still necessary to follow the safety procedures of the laboratory and avoid inhalation, intake or skin contact during use. In the event of discomfort or misuse, seek medical attention and inform the doctor of the compound used.
Last Update:2024-04-09 20:02:46