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API Candesartan cilexetil

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CAS No.:

145040-37-5

Grade:

Pharmaceutical Grade

Content:

99%

Port:

shanghai

Brand:

Hyper Chem

Packaging:

20kg/Drum 25kg/Drum

Sample Available:

Yes

Price valid (until):

2025-12-07

Company Type:
Trader
Location:
China
Payment Terms:
TT against copy of documents,D/P,L/C,D/A,O/A,TT against B/L draft before shipment,100% TT in advance
Average Lead Time:
10 days
Qualification:
Main Products:

Pharmaceuticals,Peptide,Cosmetics,Nutritional Supplements

  • Product Description

  • Seller Information

  • Inquiry History

  • Description

    Name

    Candesartan cilexetil

    CAS number

    145040-37-5 (cilexetil)

    Description

    Candesartan cilexetil is a prodrug of the potent, long-acting, and selective angiotensin II type 1 receptor (AT1) antagonist, candesartan. It is rapidly hydrolyzed to candesartan during gastrointestinal absorptio. Candesartan blocks the vasoconstrictor and aldosterone-secreting effects of angiotensin II by selectively blocking the binding of angiotensin II to the AT1 receptor in many tissues, such as vascular smooth muscle and the adrenal gland. Its action is, therefore, independent of the pathways for angiotensin II synthesis. Candesartan has much greater affinity ( > 10,000-fold) for the AT1 receptor than for the AT2 receptor.

    Appearance

    Solid powder

    Related CAS #

    139481-59-7 145040-37-5 (cilexetil)

    Synonym

    TCV-116; TCV 116; TCV116; Candesartan cilexetil

    Quality Standard

    USP, EP, BP, CP

    Shipping Condition

    Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.

    Storage Condition

    Dry, dark and at 0 - 4 ℃ for short term (days to weeks) or -20 ℃ for long term (months to years).

    Shelf Life

    >2 years if stored properly

    Sample package

    Aluminium foil bag

    Commercial package

    Aluminium Tin, Fiber drum

    Origin

    China


    Candesartan cilexetil More Info

    Candesartan cilexetil is an oral angiotensin II receptor antagonist (ARB) used primarily for managing hypertension and heart failure. It acts as a prodrug, converting to its active metabolite candesartan in the gastrointestinal tract after administration.

    Mechanism of Action

    Blocks the binding of angiotensin II to type 1 (AT₁) receptors in blood vessels, kidneys, and other tissues.

    Inhibits angiotensin II-induced vasoconstriction and sodium retention, leading to vasodilation and reduced blood volume.

    Lowers blood pressure without affecting heart rate or causing reflex tachycardia.

    Clinical Uses

    Hypertension: Monotherapy or combination therapy with other antihypertensives (e.g., diuretics, calcium channel blockers).

    Heart failure: Reduces morbidity and mortality in patients with symptomatic heart failure (NYHA classes II-IV) when added to standard therapy.

    Diabetic nephropathy: Off-label use to slow renal function decline in patients with type 2 diabetes and hypertension.

    Dosage & Administration

    Available as tablets (4 mg, 8 mg, 16 mg, 32 mg) for oral use, usually taken once daily with or without food.

    Hypertension: Initial dose 8 mg/day, titrated up to 32 mg/day based on blood pressure response.

    Heart failure: Initial dose 4 mg/day, gradually increased to 32 mg/day as tolerated.

    Dose adjustment required in patients with moderate-to-severe renal impairment or hepatic dysfunction.

    Contraindications & Precautions

    Contraindicated in patients with hypersensitivity to candesartan cilexetil, candesartan, or any excipients.

    Avoid use in pregnancy (second/third trimesters) due to risk of fetal renal damage.

    Use cautiously in patients with renal artery stenosis, hyperkalemia, or volume depletion (e.g., from diuretics).

    Monitor serum potassium and creatinine levels regularly, especially in elderly patients or those with comorbidities.

    Adverse Reactions

    Common: Dizziness, headache, fatigue, diarrhea, and upper respiratory tract infections.

    Rare: Hypotension (especially with initial dosing), hyperkalemia, renal dysfunction, and angioedema.

    Discontinue immediately if angioedema (swelling of face, lips, tongue) or severe hypotension occurs.

    Drug Interactions

    Potassium-sparing diuretics/ACE inhibitors: Increased risk of hyperkalemia.

    Nonsteroidal anti-inflammatory drugs (NSAIDs): May reduce antihypertensive effect and increase renal toxicity.

    Lithium: Increased lithium serum levels (monitor lithium concentrations).


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    ECHEMI Editorial Reference
    White SolidCandesartan cilexetil is a kind of prodrug being hydrolyzed to candesartan during absorption from the gastrointestinal tract. It appears as a white or off-white powder with a molecular weight of 610.67. It is soluble in methanol but insoluble in water. It is a kind of selective AT1 subtype angiotensin II receptor antagonist, mainly used for the treatment of hypertension and heart failure. Candesartan cilexetil takes effects through selectively blocking the binding of angiotensin II t
    Candesartan cilexetil is a member of biphenyls.|Candesartan is an angiotensin-receptor blocker (ARB) that may be used alone or with other agents to treat hypertension. It is administered orally as the prodrug, candesartan cilexetil, which is rapidly converted to its active metabolite, candesartan, during absorption in the gastrointestinal tract. Candesartan lowers blood pressure by antagonizing the renin-angiotensin-aldosterone system (RAAS); it competes with angiotensin II for binding to the type-1 angiotensin II receptor (AT1) subtype and prevents the blood pressure increasing effects of angiotensin II. Unlike angiotensin-converting enzyme (ACE) inhibitors, ARBs do not have the adverse effect of dry cough. Candesartan may be used to treat hypertension, isolated systolic hypertension, left ventricular hypertrophy and diabetic nephropathy. It may also be used as an alternative agent for the treatment of heart failure, systolic dysfunction, myocardial infarction and coronary artery disease.

    Basic Info
    Product Name:

    Candesartan cilexetil

    Other Name:

    1H-Benzimidazole-7-carboxylic acid,2-ethoxy-1-[[2′-(2H-tetrazol-5-yl)[1,1′-biphenyl]-4-yl]methyl]-,1-[[(cyclohexyloxy)carbonyl]oxy]ethyl ester;1H-Benzimidazole-7-carboxylic acid,2-ethoxy-1-[[2′-(1H-tetrazol-5-yl)[1,1′-biphenyl]-4-yl]methyl]-,1-[[(cyclohexyloxy)carbonyl]oxy]ethyl ester,(±)-;1H-Benzimidazole-7-carboxylic acid,2-ethoxy-1-[[2′-(1H-tetrazol-5-yl)[1,1′-biphenyl]-4-yl]methyl]-,1-[[(cyclohexyloxy)carbonyl]oxy]ethyl ester;TCV 116;(±)-1-Hydroxyethyl 2-ethoxy-1-[p-(o-1H-tetrazol-5-ylphenyl)l]-7-benzimidazolecarboxylate,cyclohexyl carbonate (ester);Candesartan cilexetil;Atacand;TCY 116;Blopress;2-Ethoxy-1-[(2′-(1H-tetrazol-5-yl)-1,1′-biphenyl-4-yl)methyl]-7-benzimidazolecarboxylic acid 1-(cyclohexyloxycarbonyloxy)ethyl ester;1-[[(Cyclohexyloxy)carbonyl]oxy]ethyl 2-ethoxy-1-[[2′-(1H-tetrazol-5-yl)biphenyl-4-yl]methyl]benzimidazole-7-carboxylate;1-Cyclohexyloxycarbonyloxyethyl 2-ethoxy-3-[[4-[2-(2H-tetrazol-5-yl)phenyl]phenyl]methyl]benzimidazole-4-carboxylate;1-[[(Cyclohexyloxy)carbonyl]oxy]ethyl 2-ethoxy-1-([4-[2-(1H-1,2,3,4-tetrazol-5-yl)phenyl]phenyl]methyl)-1H-1,3-benzodiazole-7-carboxylate;139481-74-6;198077-85-9;2050948-41-7

    CAS No.:

    145040-37-5

    Molecular Formula:

    C33H34N6O6

    InChIKeys:

    InChIKey=GHOSNRCGJFBJIB-UHFFFAOYSA-N

    Molecular Weight:

    610.66

    Exact Mass:

    610.66

    EC Number:

    1592732-453-0

    NSC Number:

    758697

    DSSTox ID:

    DTXSID5020239

    HScode:

    29339953

    Characteristics
    PSA:

    143

    XLogP3:

    7

    Appearance:

    white to beige

    Density:

    1.37±0.1 g/cm3(Predicted)

    Melting Point:

    163 °C (decomp)

    Boiling Point:

    843.3±75.0 °C(Predicted)

    Flash Point:

    463.8±37.1 °C

    Refractive Index:

    1.667

    Water Solubility:

    DMSO: ≥15mg/mL

    Storage Conditions:

    -20°C Freezer

    Collision Cross Section:

    241.5 Ų [M+H]+ [CCS Type: TW, Method: calibrated with polyalanine and drug standards]

    Hazard Identification

    Classification of the substance or mixture

    Reproductive toxicity, Category 2

    GHS label elements, including precautionary statements

    Pictogram(s)
    Signal word

    Warning

    Hazard statement(s)

    H361 Suspected of damaging fertility or the unborn child

    Precautionary statement(s)
    Prevention

    P203 Obtain, read and follow all safety instructions before use.

    P280 Wear protective gloves/protective clothing/eye protection/face protection/hearing protection/...

    Response

    P318 IF exposed or concerned, get medical advice.

    Storage

    P405 Store locked up.

    Disposal

    P501 Dispose of contents/container to an appropriate treatment and disposal facility in accordance with applicable laws and regulations, and product characteristics at time of disposal.

    Other hazards which do not result in classification

    no data available

    Handling and Storage

    Precautions for safe handling

    Handling in a well ventilated place. Wear suitable protective clothing. Avoid contact with skin and eyes. Avoid formation of dust and aerosols. Use non-sparking tools. Prevent fire caused by electrostatic discharge steam.

    Conditions for safe storage, including any incompatibilities

    Store the container tightly closed in a dry, cool and well-ventilated place. Store apart from foodstuff containers or incompatible materials.

  • Seller Information
    Business Type:

    Trader

    Main Products:

    Pharmaceuticals,Peptide,Cosmetics,Nutritional Supplements

    Location:

    Rm. 803, Tower 4, LOFT49 Creative City Pioneer Zone, No.88 Jiru Rd. Gongshu Dist., Hangzhou, 310015 ZJ, China

    Payment Terms:

    TT against copy of documents,D/P,L/C,D/A,O/A,TT against B/L draft before shipment,100% TT in advance

    Average lead Time:

    10 days

    Total Annual Revenue:

    $5 million-$10 million

    Total Employees:

    11-50

    Year of Establishment:

    2013

    Company Certificates
    • Hangzhou Hyper Chemicals LimitedCertification Report by Bureau Veritas Certification Report by Bureau Veritas
    About HyperChem

    Established in 2013, Hyper Chem has exclusive tie-ups with leading manufacturers, supplying raw materials produced in GMP and ISO 9002 certified facilities, and provides high-quality ingredients and raw materials to meet the needs of a diverse range of pharmaceutical cosmetics ingredients and nootropic supplements companies worldwide.

    Our Competitiveness

    One-stop supply

    Wide Range Of products including pharmaceutical, Cosmetic Ingredients and nootropic supplements

    Among all the pharmaceuticals,

    90% of them with GMP certificates,

    85% of them with DMF files and

    50% of them passed FDA approval,

    30% get CEP certificate

    20% are new R&D products.

    Custom Repackaging Service


    We can efficiently repackage your material into sample sizes, custom batch-specific sizes, or semi-bulk package sizes according to your specifications. And ensures the product is packaged in a quality-controlled environment and will maintain its integrity throughout every stage of the process.

    Quality Control/Quality Assurance


    HyperChem is committed to delivering on its promises of top-quality products with verified quality data.

    All materials are vigorously inspected by the factory and/or outsourced analytical laboratories to ensure each and every lot meets or exceeds our reference standards.

    Trade assurance service with 100% payment protection, It is best achieved by delivering products and services 100% right the first time, on time, every time.

    Professional

    Transparent Communication

    Fast Reaction,

    Professional Suggestion

    Beyond Expectation.

    We have exclusive partnerships with research and production facilities across the country and we offer varied pharmaceutical services in the most cost-efficient way. The production facilities are GMP, WHO-GMP, EU GMP and US FDA approved and are backed by strong regulatory support such as Dossier, DMF, Tech Pack and relevant Stability studies for regulatory filings.

  • Inquiry History
    1 Inquiries
    Country Product Purchase Quantity Date Posted
    Vietnam

    Candesartan cilexetil

    5 KG May 16, 2026
    Post an enquiry for this product
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