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Ethynylestradiol Reference Materials

Unlock Precision in Residue Analysis with High-Purity Ethynylestradiol Reference Materials

Ensure your laboratorys accuracy and compliance with HPC Standards GmbHs high-purity Ethynylestradiol reference materials. Our products meet the highest international quality standards, making them indispensable for food and environmental analysis. Trust in our expertise to deliver reliable results for your residue analysis needs.

Product

Catalog No./ CAS No.

Quantity

Price

13C2-17-alpha-Ethinylestradiol solution
Concentration: 100 µg/ml
Solvent: Acetonitrile

13C2-17-alpha-Ethinylestradiol solution

683803

1X1ML

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17a-Ethinylestradiol

17a-Ethinylestradiol

672998
57-63-6

1X250MG

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17a-Ethinylestradiol solution
Concentration: 100 µg/ml
Solvent: Methanol

17a-Ethinylestradiol solution

677782
57-63-6

1X1ML

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D4-17-alpha-Ethinylestradiol

D4-17-alpha-Ethinylestradiol

687159
350820-06-3

1X5MG

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D4-17-alpha-Ethinylestradiol solution
Concentration: 100 µg/ml
Solvent: D4-Methanol

D4-17-alpha-Ethinylestradiol solution

687160
350820-06-3

1X1ML

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High-Purity Reference Materials for Accurate Residue Analysis

Overview

Ethynylestradiol (EE) is a synthetic estrogen widely used in combination with progestins in birth control pills. It is also used in menopausal hormone therapy and the treatment of certain hormone-sensitive cancers. EE is known for its high oral bioavailability and resistance to metabolism, making it a prevalent choice in contraceptive formulations.

Uses

EE is primarily used in combined oral contraceptives (COCs) to prevent pregnancy. It is also utilized in menopausal hormone therapy to alleviate symptoms such as hot flashes and vaginal dryness. Additionally, EE has applications in treating hypogonadism, osteoporosis prevention, and as part of feminizing hormone therapy for transgender women.

Regulatory

EE is a prescription-only medication with stringent regulatory controls due to its potent biological effects and potential side effects. It is included in various international pharmacopeias and must meet rigorous quality standards.

Monitoring

Regular monitoring of EE levels is essential in clinical settings to ensure therapeutic efficacy and minimize adverse effects. Analytical methods such as liquid chromatography-mass spectrometry (LC-MS) are commonly used for this purpose.

Health Impact

Human Toxicity

Common side effects of EE include breast tenderness, headache, fluid retention, and nausea. In men, it can cause feminization and hypogonadism. Serious but rare side effects include blood clots, liver damage, and uterine cancer.

Environmental Impact

Effects on Wildlife

EE can enter freshwater ecosystems through wastewater, affecting fish and amphibian populations. Chronic exposure can lead to reproductive issues and population declines in aquatic species.

Safety Measures

Proper handling and disposal of EE are crucial to minimize environmental contamination. Laboratories must follow safety protocols to protect personnel and the environment.

Regulation

EE is regulated under various national and international guidelines, including those from the FDA and EMA. Compliance with these regulations ensures the safe and effective use of EE in medical and research applications.

Analytical Standards

HPC Standards GmbH provides high-purity reference materials for EE, tested according to international quality requirements. These materials are essential for accurate residue analysis in food and environmental samples, ensuring compliance with regulatory limits.