Telmisartan

Telmisartan

Parametro Specifiche
Nome del prodotto Telmisartan
Numero CAS 144701-48-4
Formula molecolare C33H30N4O2
Peso molecolare 514.62 g/mol
Aspetto Polvere cristallina di colore da bianco a bianco sporco
Analisi (HPLC) ≥ 99,01 TP3T
Solubilità Soluble in DMSO, slightly soluble in ethanol, practically insoluble in water
Confezione 25 kg fiber drum with double polyethylene liner

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Telmisartan Structure

Sinonimi: Telmisartan, 144701-48-4, Micardis, Pritor, Kinzal, BIBR 277, Telmisartanum

Telmisartan is a non-peptide angiotensin II receptor blocker (ARB) that selectively antagonizes the AT1 receptor subtype. It was developed by Boehringer Ingelheim and has been a cornerstone in the management of hypertension and cardiovascular risk reduction since its approval in the late 1990s. Unlike many other ARBs, telmisartan possesses a unique biphenyl carboxylic acid structure that confers high lipophilicity and a long duration of action.

Its molecular formula is C33H30N4O2, with a molecular weight of 514.62 g/mol. The compound is practically insoluble in water but freely soluble in DMSO and slightly soluble in ethanol. This solubility profile, along with its high melting point, makes it a stable and manageable API for solid dosage forms.

As a generic API, telmisartan is standardized to ≥99.0% purity (HPLC) and is widely used in the manufacture of immediate-release tablets, often in combination with hydrochlorothiazide or amlodipine. Its well-established efficacy and safety profile have made it a preferred choice for formulators targeting the global cardiovascular market.

Function & Mechanism

  • Angiotensin II receptor blockade: Telmisartan selectively blocks the AT1 receptor, preventing the vasoconstrictive and aldosterone-secreting effects of angiotensin II.
  • Blood pressure reduction: By inhibiting AT1, it lowers systemic vascular resistance and reduces blood pressure without affecting heart rate.
  • Cardiovascular protection: It may also provide end-organ protection, particularly in patients with diabetes or heart failure.
  • Partial PPAR-γ agonism: Telmisartan exhibits unique partial agonist activity at PPAR-γ, which may contribute to improved insulin sensitivity and metabolic effects.

Fonte e standardizzazione

  • Fonte: Synthetic chemical synthesis
  • Manufacturing process: Multi-step organic synthesis followed by purification and crystallization
  • Standardizzazione: ≥99.0% (HPLC)
  • Moduli: White to off-white crystalline powder
  • Applicazioni: API for antihypertensive tablets, fixed-dose combinations, and clinical research

Quality Specifications (QC Tests)

Test Item Specifiche
Identificazione IR, HPLC retention time conforms to standard
Perdita per essiccazione ≤ 0,51 TP3T
Residuo di combustione ≤ 0,11 TP3T
Metalli pesanti ≤ 10 ppm
Organic Impurities Any individual impurity ≤ 0.2%, total impurities ≤ 0.5%
Solventi residui Meets ICH Q3C requirements
Limiti microbiologici Total aerobic count ≤ 1000 CFU/g, yeast and mold ≤ 100 CFU/g, absence of E. coli

Bulk Supply & Documentation

  • Capacità mensile: 5 tonnellate metriche
  • Tempi di consegna: 3-5 business days (stock items)
  • Documentazione: COA, MSDS, TDS, DMF available upon request
  • Confezionamento: 25 kg fiber drum with double polyethylene liner, or as per customer requirements

Frequently Asked Questions

What is the minimum order quantity (MOQ)?

Our standard MOQ is 1 kg, but we can accommodate smaller quantities for research and development purposes.

Do you provide a Certificate of Analysis (COA) and samples?

Yes, we provide a COA for each batch and can offer samples for evaluation upon request.

What is the typical lead time?

Standard lead time is 3-5 business days after order confirmation, depending on quantity and destination.

Contact & Ordering Information

  • Company: LyvBio Co., Ltd.
  • Address: Room 5-0203, Courtyard 205, Lianhu District, Xi’an, Shaanxi, China
  • Email: info@lyvbio.com
  • Phone: +86-29-65816888

Learn more about our quality control and certifications, or send us your specification for a quotation.

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