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High-Purity (Z)-8-Dodecen-1-yl Acetate (CAS 28079-04-1): The Essential Pheromone Intermediate for Sustainable Pest Management

In the rapidly evolving landscape of sustainable agriculture and integrated pest management (IPM), the demand for high-purity semiochemicals has never been greater. FINETECH INDUSTRY LIMITED is proud to offer premium-grade (Z)-8-Dodecen-1-yl Acetate (CAS: 28079-04-1), a critical component in the manufacturing of sex pheromones for various lepidopteran species.Technical SpecificationsProduct Name: (Z)-8-Dodecen-1-yl AcetateCAS Number: 28079-04-1Molecular Formula: C14}H26O2Molecular Weight: 226.35 g/molPurity: ≥95% Appearance: Colorless to light yellow liquidStrategic Importance in Agricult [...]

Jun 18, 2026 Product News 247 Views Read More

Introduction to (-)-Methyl (R)-3-Hydroxypentanoate (CAS: 60793-22-8)

(-)-Methyl (R)-3-Hydroxypentanoate, also known as (R)-3-Hydroxypentanoic acid methyl ester, is an organic compound with a specific stereochemical configuration. It is commonly referred to as (-)-Methyl (R)-3-Hydroxypentanoate and is identified by its CAS number: 60793-22-8. This compound has attracted attention in various fields due to its potential applications and unique properties.Chemical Properties:(-)-Methyl (R)-3-Hydroxypentanoate is an ester derivative of (R)-3-Hydroxypentanoic acid. It possesses a chiral center with a specific (R)-configuration, indicating its stereochemistry. The com [...]

Jun 18, 2026 Product News 6337 Views Read More

Idarubicin: Mechanism of Action, Side Effects, and Clinical Applications in Cancer Treatment

Idarubicin 57852-57-0is a potent chemotherapy drug belonging to the anthracycline class, primarily used in the treatment of various types of cancer, including acute myeloid leukemia (AML) and acute lymphocytic leukemia (ALL). Its mechanism of action, side effects, and clinical applications make it a crucial component of cancer treatment regimens.Mechanism of Action:Idarubicin exerts its anticancer effects by interfering with the DNA and RNA synthesis of cancer cells. It does so by intercalating between DNA base pairs, inhibiting the activity of topoisomerase II enzyme, and generating free radi [...]

Jun 17, 2026 Product News 1443 Views Read More