Enclomiphene citrate

Synonyme: trans-Clomiphene citrate, (E)-Clomiphene citrate, Enclomiphene dihydrogen citrate, 2-[4-[(E)-2-chloro-1,2-diphenylethenyl]phenoxy]-N,N-diethylethanamine citrate

Enclomiphene citrate is the trans-isomer of clomiphene citrate, a selective estrogen receptor modulator (SERM) that has drawn considerable attention in both clinical research and pharmaceutical manufacturing. Unlike its cis counterpart zuclomiphene, which exhibits estrogenic activity, enclomiphene acts as a pure estrogen antagonist in the hypothalamus and pituitary. This distinct pharmacological profile has positioned it as a compound of interest for developing therapies targeting testosterone deficiency and related endocrine disorders.

Chemically, enclomiphene citrate belongs to the triphenylethylene class, sharing structural similarities with tamoxifen and other well-known SERMs. The molecule features a chloro-substituted stilbene core with a diethylaminoethoxy side chain, and its citrate salt form enhances aqueous solubility and stability. The trans configuration is critical for its antagonistic properties; even minor contamination with the cis isomer can significantly alter the pharmacological response, making stereochemical purity a key quality parameter.

In the pharmaceutical supply chain, enclomiphene citrate is typically produced under cGMP conditions and is available in high-purity grades suitable for formulation development and clinical trial materials. It is most commonly used in the development of oral capsules or tablets for hormone modulation, and as a reference standard in analytical laboratories. Its rising profile in men’s health research has led to increased demand for reliable, well-documented sources of this active pharmaceutical ingredient.

Funktion

• Selective estrogen receptor modulation: Blocks estrogen receptors in the hypothalamus, leading to increased gonadotropin-releasing hormone (GnRH) secretion.
• Testosterone stimulation: Enhances endogenous testosterone production by promoting LH and FSH release from the pituitary.
• Fertility support: Investigated for improving spermatogenesis and ovulation induction in specific patient populations.
• Hormonal balance: Helps restore normal testosterone-to-estrogen ratios in men with secondary hypogonadism.
• Research applications: Used as a tool compound in studies of estrogen receptor signaling and endocrine regulation.

Source & Standardization

• Quelle: Synthetic chemical synthesis; not derived from natural sources.
• Manufacturing: Produced via a multi-step organic synthesis, followed by chiral resolution or stereoselective synthesis to isolate the trans isomer.
• Standardization: ≥98.0% assay (HPLC), with strict control of cis-isomer content (typically ≤0.5%).
• Forms: White to off-white crystalline powder.
• Anwendungen: Pharmaceutical formulations, clinical research, analytical reference standards.

Technische Daten

Documentation & Supply

• Monthly capacity: 50 kg
• Lieferzeit: 3–5 Werktage (Lagerware)
• Dokumentation: COA, MSDS, TDS, stability data, and cGMP compliance statements available upon request
• Verpackung: 25 kg fiber drum with double polyethylene liner; custom packaging options available

Angebotsanfrage

• LyvBio GmbH. — E-Mail: info@lyvbio.com