Diltiazem HCl - ≥98% , CAS No.33286-22-5

CAS: 33286-22-5 Cat. No.: C154045 Formula: C22H26N2O4S·HCl Peso molecolare: 450.98 Numero EC: 251-443-3
Disponibile su ordine
GRADE & PURITY ≥98%
Synonyms
CRD-401 | (+)-cis-Diltiazem cloridrato | Britiazim | Farmabes | Myonil | Cardizem Retard | Gadoserin | Presoken | Dinisor Retard | Cardizem LA | Diltan | Miocardie | Bruzem | Diltiasyn | Diltiazem GNR | Tiadil | Mono-Tildiem | Syn-Diltiazem | Apo-dilti
Storage
Conservare a 2-8°C, con carica di argon
Shipped In
Ghiaccio umido
★
Size
Germania (EU)
USA*
Price
Qty
1g
C154045-1g
—
5 Disponibile
34,62€
5g
C154045-5g
—
8 Disponibile
71,07€
25g
C154045-25g
—
3 Disponibile
235,94€
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Conservare a 2-8°C, con carica di argon Ships Ghiaccio umido Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Panoramica

Il diltiazem cloridrato (Tiazac) è un derivato della benzotiazepina con azione vasodilatatrice dovuta all'antagonismo delle azioni dello ione calcio nelle funzioni di membrana. Il diltiazem cloridrato è utilizzato per il trattamento delle malattie cardiovascolari, come l'angina e l'ipertensione. Agisce come inibitore del citocromo P450 3A (CYP3A). Il diltiazem può essere associato a eruzioni maculopapulari, orticaria e prurito.

Specifications

Sinonimi
CRD-401 | (+)-cis-Diltiazem cloridrato | Britiazim | Farmabes | Myonil | Cardizem Retard | Gadoserin | Presoken | Dinisor Retard | Cardizem LA | Diltan | Miocardie | Bruzem | Diltiasyn | Diltiazem GNR | Tiadil | Mono-Tildiem | Syn-Diltiazem | Apo-dilti
Specifiche e purezza
≥98%
Meccanismi biochimici e fisiologici
Blocca i canali del Ca2+ lenti o di tipo L; regola il rilascio di Ca2+ dai depositi intracellulari nei neutrofili; stimola il legame della 1,4-diidropiridina ai canali del Ca2+; vasodilatatore coronarico.Antagonista dei canali del Ca 2+ di tipo L. Vasodil
Condizioni di conservazione di stoccaggio
Conservare a 2-8°C, con carica di argon
Spedito in
Ghiaccio umido
Nota
Per quanto possibile, si consiglia di preparare e utilizzare le soluzioni lo stesso giorno. Tuttavia, se è necessario preparare in anticipo le soluzioni di riserva, si consiglia di conservarle in aliquote in fiale ben chiuse a -20°C. In genere, queste possono essere utilizzate per un mese. In genere, queste soluzioni sono utilizzabili fino a un mese. Prima dell'uso e dell'apertura della fiala, si consiglia di lasciare che il prodotto si equilibri a temperatura ambiente per almeno 1 ora. Avete bisogno di ulteriori consigli su solubilità, uso e manipolazione? Per ulteriori informazioni, visitare la pagina delle domande frequenti (FAQ).
Purezza
≥98%
Nomi e identificatori
Pubchem Sid504753891
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504753891
Sorrisi canoniciCC(=O)OC1C(SC2=CC=CC=C2N(C1=O)CCN(C)C)C3=CC=C(C=C3)OC.Cl
IUPAC Name[(2S,3S)-5-[2-(dimethylamino)ethyl]-2-(4-methoxyphenyl)-4-oxo-2,3-dihydro-1,5-benzothiazepin-3-yl] acetate;hydrochloride
InChIKeyHDRXZJPWHTXQRI-BHDTVMLSSA-N
INCHI1S/C22H26N2O4S.ClH/c1-15(25)28-20-21(16-9-11-17(27-4)12-10-16)29-19-8-6-5-7-18(19)24(22(20)26)14-13-23(2)3;/h5-12,20-21H,13-14H2,1-4H3;1H/t20-,21+;/m1./s1
Isomeri SMILES CC(=O)O[C@@H]1[C@@H](SC2=CC=CC=C2N(C1=O)CCN(C)C)C3=CC=C(C=C3)OC.Cl
WGK Germania 3
RTECS DL0310000
CAS alternativo 42399-41-7
Peso molecolare 450.98
Reaxy-Rn 6889420
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=6889420&ln=

Documentazione

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClasseBenzothiazepines
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentBenzothiazepines
Alternative Parents Phenoxy compounds  Methoxybenzenes  Anisoles  Alkyl aryl ethers  Alkylarylthioethers  Tertiary carboxylic acid amides  Trialkylamines  Lactams  Amino acids and derivatives  Carboxylic acid esters  Monocarboxylic acids and derivatives  Azacyclic compounds  Carbonyl compounds  Hydrocarbon derivatives  Hydrochlorides  Organic oxides  Organopnictogen compounds  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Benzothiazepine - Anisole - Phenol ether - Methoxybenzene - Aryl thioether - Phenoxy compound - Alkyl aryl ether - Alkylarylthioether - Monocyclic benzene moiety - Benzenoid - Tertiary carboxylic acid amide - Amino acid or derivatives - Carboxamide group - Tertiary aliphatic amine - Carboxylic acid ester - Tertiary amine - Lactam - Azacycle - Carboxylic acid derivative - Thioether - Ether - Monocarboxylic acid or derivatives - Organic oxygen compound - Hydrocarbon derivative - Hydrochloride - Carbonyl group - Organic nitrogen compound - Organopnictogen compound - Amine - Organic oxide - Organonitrogen compound - Organooxygen compound - Aromatic heteropolycyclic compound
DescrizioneThis compound belongs to the class of organic compounds known as benzothiazepines. These are organic compounds containing a benzene fused to a thiazepine ring (a seven-membered ring with a nitrogen atom and a sulfur atom replacing two carbon atoms).
External Descriptors hydrochloride
Struttura 3D
Modello di struttura chimica interattiva





Obiettivi associati (umani)
THRB Tclin Thyroid hormone receptor beta-1 (7926 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
U2OS (164939 Activities)
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HEK293 (82097 Activities)
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EHMT2 Tchem Histone-lysine N-methyltransferase, H3 lysine-9 specific 3 (93046 Activities)
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LMNA Tbio Prelamin-A/C (36751 Activities)
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BLM Tchem Bloom syndrome protein (4248 Activities)
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SMAD3 Tchem Mothers against decapentaplegic homolog 3 (68039 Activities)
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GMNN Tbio Geminin (128009 Activities)
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KMT2A Tchem Histone-lysine N-methyltransferase MLL (17327 Activities)
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SLCO1B1 Tchem Solute carrier organic anion transporter family member 1B1 (2672 Activities)
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MPHOSPH8 Tbio M-phase phosphoprotein 8 (656 Activities)
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SLCO1B3 Tchem Solute carrier organic anion transporter family member 1B3 (2517 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MEN1 Tchem Menin/Histone-lysine N-methyltransferase MLL (48157 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
RUNX1 Tbio Runt-related transcription factor 1/Core-binding factor subunit beta (7867 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HEK-293T (167025 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Obiettivi associati (non umani)
Pseudomonas aeruginosa (123386 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Klebsiella pneumoniae (43867 Activities)
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Staphylococcus aureus (210822 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Acinetobacter baumannii (41033 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Escherichia coli (133304 Activities)
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Cryptococcus neoformans (21258 Activities)
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Candida albicans (78123 Activities)
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Cavia porcellus (23802 Activities)
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Canis familiaris (36305 Activities)
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Mus musculus (284745 Activities)
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Brain (1 Activities)
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Plasma (328 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ffp 4'-phosphopantetheinyl transferase ffp (24982 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NS1 Nonstructural protein 1 (33327 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Meccanismi d'azione
Certificati (CoA, COO, BSE/TSE e tabella di analisi)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

7 results found

Lot NumberCertificate TypeDataOggetto
K2201092Certificate of AnalysisAug 03, 2026 C154045
K2201095Certificate of AnalysisAug 03, 2026 C154045
J2127662Certificate of AnalysisAug 11, 2025 C154045
J2127663Certificate of AnalysisAug 11, 2025 C154045
F2425197Certificate of AnalysisApr 02, 2024 C154045
F2425198Certificate of AnalysisApr 02, 2024 C154045
K2330171Certificate of AnalysisJul 28, 2022 C154045
Proprietà chimiche e fisiche
SolubilitàSoluble in water at 50mg/ml
SensibilitàAir & light & heat sensitive
Rotazione specifica [α]114 to 122 deg(C=1, H2O)
Punto di fusione (°C)210 °C
Peso molecolare451.000 g/mol
XLogP3
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count6
Rotatable Bond Count7
Exact Mass450.138 Da
Monoisotopic Mass450.138 Da
Topological Polar Surface Area84.400 Ų
Heavy Atom Count30
Formal Charge0
Complexity565.000
Isotope Atom Count0
Defined Atom Stereocenter Count2
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count2
Citations of This Product
Riferimenti
1. Wang Yiran, Shi Jihua, Dai Dapeng, Cai Jianping, Wang Shuanghu, Hong Yun, Zhou Shan, Zhao Fangling, Zhou Quan, Geng Peiwu, Zhou Yunfang, Xu Xue, Luo Qingfeng.  (2022)  Evaluation of commonly used cardiovascular drugs in inhibiting vonoprazan metabolism in vitro and in vivo.  Frontiers in Pharmacology,      [PMID:36052128] [10.3389/fphar.2022.909168]
Calcolatori di soluzioni
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