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Diltiazem hydrochloride

CAS No.
33286-22-5
Chemical Name:
Diltiazem hydrochloride
Synonyms
DILTIAZEM HCL;DILTHIAZEM HYDROCHLORIDE;Tiazac;Sprix;Acuvail;cardizem;herbesser;Dilacor XR;Diltiazem Hydrochlorid;(2S,cis)-3-(Acetyloxy)-5-[(2-dimethylamino)ethyl]-2,3-dihydro-2-(4-methoxyphenyl)-1,5-benzothiazepin-4(5H)-one Hydrochloride
CBNumber:
CB7302994
Molecular Formula:
C22H27ClN2O4S
Molecular Weight:
450.98
MDL Number:
MFCD00069252
MOL File:
33286-22-5.mol
MSDS File:
SDS
Last updated:2024-11-19 23:02:33

Diltiazem hydrochloride Properties

Melting point 212-214 °C
alpha D24 +98.3 ± 1.4° (c = 1.002 in methanol)
Density 1.30 g/cm3
refractive index 118 ° (C=1, H2O)
Flash point 2℃
storage temp. 2-8°C
solubility Freely soluble in water, in methanol and in methylene chloride, slightly soluble in anhydrous ethanol.
form Powder
color White to off-white
PH pH (10g/l, 25℃) : 4.3~5.3
Water Solubility soluble
Merck 13,3226
BRN 4228706
Stability Stable for 1 year from date of purchase as supplied. Solutions in DMSO or distilled water may be stored at -20°C for up to 3 months.
CAS DataBase Reference 33286-22-5(CAS DataBase Reference)
FDA UNII OLH94387TE
Proposition 65 List Diltiazem Hydrochloride
NCI Drug Dictionary Cardizem
EPA Substance Registry System 1,5-Benzothiazepin-4(5H)-one, 3-(acetyloxy)-5-[2-(dimethylamino)ethyl]-2,3-dihydro-2-(4-methoxyphenyl)-, hydrochloride (1:1), (2S,3S)- (33286-22-5)

Pharmacokinetic data

Protein binding 80-85%
Excreted unchanged in urine 5%
Volume of distribution 3-8(L/kg)
Biological half-life 2-11; SR: 5-8 / Unchanged

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302
Precautionary statements  P301+P312+P330
Hazard Codes  Xn,Xi,F
Risk Statements  22-40-36/37/38-36-20/21/22-11
Safety Statements  36-45-36/37-26-16
RIDADR  3249
WGK Germany  3
RTECS  DL0310000
8-10
HazardClass  6.1(b)
PackingGroup  III
HS Code  29349990
Toxicity LD50 in male, female mice, male, female rats (mg/kg): 61, 58, 38, 39 i.v.; 260, 280, 520, 550 s.c.; 740, 640, 560, 610 orally (Nagao, 1972)
NFPA 704
0
2 0

Diltiazem hydrochloride price More Price(50)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich PHR2856 Diltiazem Hydrochloride certified reference material, pharmaceutical secondary standard 33286-22-5 500MG $218 2024-03-01 Buy
Sigma-Aldrich D-035 Diltiazem hydrochloride solution 1.0?mg/mL in acetonitrile (as free base), ampule of 1?mL, certified reference material, Cerilliant? 33286-22-5 1mL $69 2024-03-01 Buy
Sigma-Aldrich 309866 Diltiazem, Hydrochloride Synthetic benzothiazepine that acts as an L-type Ca 33286-22-5 100mg $96.7 2024-03-01 Buy
Sigma-Aldrich 1205003 Diltiazem hydrochloride United States Pharmacopeia (USP) Reference Standard 33286-22-5 200mg $436 2024-03-01 Buy
Sigma-Aldrich BP899 Diltiazem impurity standard British Pharmacopoeia (BP) Reference Standard 33286-22-5 25MG $227 2023-01-07 Buy
Product number Packaging Price Buy
PHR2856 500MG $218 Buy
D-035 1mL $69 Buy
309866 100mg $96.7 Buy
1205003 200mg $436 Buy
BP899 25MG $227 Buy

Diltiazem hydrochloride Chemical Properties,Uses,Production

Description

Diltiazem HCl (33286-22-5) is a?non-dihydropyridine-type blocker of L-type Ca2+ channels.1,2 Reduces Ca2+ oscillations in subcellular compartments in vascular smooth muscle cells.3?Also blocks P-type Ca2+ channels in freshly dissociated rat cerebellar Purkinje neurons.4 Clinically useful antihypertensive agent.5?Cell permeable.

Chemical Properties

Diltiazem hydrochloride is a white to off-white crystalline powder with a bitter taste. It is soluble in water, methanol, and chloroform. It has a molecular weight of 450.98. Diltiazem hydrochloride injection is a clear, colorless, sterile, nonpyrogenic solution. It has a pH range of 3.7 to 4.1.

Originator

Herbesser,TANABE SEIYAKU,Japan,1974

Uses

Peripheral Vasodilator

Uses

antihypertensive, sedative, antibacterial

Uses

Diltiazem Hydrochloride is a calcium channel blocker with vasodilating activity. Anti-anginal; anti-hypertensive; anti-arrhythmic (class IV).

Uses

An antianginal, antihypertensive. Regulates Calcium release from intracellular stores in neutrophils

Definition

ChEBI: Diltiazem hydrochloride is a hydrochloride salt resulting from the reaction of equimolar amounts of diltiazem and hydrogen chloride. A calcium-channel blocker and vasodilator, it is used in the management of angina pectoris and hypertension. It has a role as an antihypertensive agent, a vasodilator agent and a calcium channel blocker. It contains a diltiazem(1+). It is an enantiomer of an ent-diltiazem hydrochloride.

Manufacturing Process

β-Diethylaminoethyl chloride is condensed with 2-(4-methoxyphenyl)-3- hydroxy-2,3-dihydro-1,5-benzothiazepin-4(5H)-one in a first step. Then a mixture of 1.5 grams of 2-(4-methoxyphenyl)-3-hydroxy-5-(βdimethylaminoethyl)-2,3-dihydro-1,5-benzothiazepin-4(5H)-one and 20 ml of acetic anhydride was heated on a water bath for 5 hours. The reaction mixture was evaporated under reduced pressure to remove acetic anhydride and the concentrated product was poured into ice water. The resulting mixture was made alkaline with sodium bicarbonate and extracted with chloroform. The chloroform layer was dried and evaporated to remove the solvent. The residue was dissolved in acetone, and an ethanol solution containing hydrogen chloride was added thereto producing 1.53 grams of 2-(4-methoxyphenyl)3- acetoxy-5-(β-dimethylaminoethyl)-2,3-dihydro-1,5-benzothiazepin-4(5H)-one hydrochloride having a melting point from 187° to 188°C.
The starting material is made by reacting 4-methoxybenzaldehyde with ethyl chloroacetate; that product with sodium ethoxide; and that product with 2- aminothiophenol.

brand name

Cardizem (Biovail); Cartia (Andrx); Dilacor (Watson); Diltzac (Apotex); Taztia (Andrx); Tiazac (Biovail).

Therapeutic Function

Coronary vasodilator

General Description

Diltiazem hydrochloride is a calcium ion cellular influx inhibitor. It was developed and introduced inJapan as a cardiovascular agent to treat angina pectoris. Itwas observed to dilate peripheral arteries and arterioles. Thedrug increases myocardial oxygen supply by relieving coronaryartery spasm and reduces myocardial oxygen demandby decreasing heart rate and reducing overload. Diltiazemhydrochloride is used in patients with variant angina. Thedrug has electrophysiological properties similar to those ofverapamil and is used in clinically similar treatment conditionsas an antiarrhythmic agent, but it is less potent.
The drug is absorbed rapidly and almost completely fromthe digestive tract. It reaches peak plasma levels within 1hour after administration in gelatin capsules. Oral formulationson the market are sustained-release preparations providingpeak plasma levels 3 to 4 hours after administration.

Biological Activity

Antihypertensive and cardioprotective agent; an inhibitor of L-type Ca 2+ channels.

Biochem/physiol Actions

Product does not compete with ATP.

Clinical Use

Calcium-channel blocker:
Prophylaxis and treatment of angina
Hypertension

Metabolism

Diltiazem is almost completely absorbed from the gastrointestinal tract after oral doses, but undergoes extensive first-pass hepatic metabolism resulting in a bioavailability of about 40%. It is extensively metabolised in the liver, mainly by the cytochrome P450 isoenzyme CYP3A4; one of the metabolites, desacetyldiltiazem, has been reported to have 25-50% of the activity of the parent compound
About 2-4% of a dose is excreted in urine as unchanged diltiazem with the remainder excreted as metabolites in bile and urine.

storage

Store at RT

Mode of action

Diltiazem Hydrochloride is a benzothiazepine calcium channel blocking agent. Diltiazem hydrochloride inhibits the transmembrane influx of extracellular calcium ions into select myocardial and vascular smooth muscle cells, causing dilatation of coronary and systemic arteries and decreasing myocardial contractility. Because of its vasodilatory activity, this agent has been shown to improve the microcirculation in some tumors, thereby potentially improving the delivery of antineoplastic agents to tumor cells.

References

1) Kraus?et al.?(1998),?Molecular mechanism of diltiazem interaction with L-type Ca2+ channels; J. Biol. Chem.,?273?27205 2) Godfraind?et al. (1986),?Calcium antagonism and calcium entry blockade; Pharmacol. Rev.,?38?321 3) Fedoryak?et al.?(2004),?Spontaneous Ca2+ oscillations in subcellular compartments of vascular smooth muscle cells rely on different Ca2+ pools; Cell Res.,?14?379 4) Ishibashi?et al. (1995),?Block of P-type Ca2+ channels in freshly dissociated rat cerebellar Purkinje neurons by diltiazem and verapamil; Brain Res.,?695?88 5) Chaffman and Bogden (1985),?Diltiazem. A review of its pharmacological properties and therapeutic efficacy; Drugs,?29?387

42399-40-6
108-24-7
33286-22-5
Synthesis of Diltiazem hydrochloride from Deacetyldiltiazem and Acetic anhydride
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View Lastest Price from Diltiazem hydrochloride manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Diltiazem hydrochloride pictures 2024-11-19 Diltiazem hydrochloride
33286-22-5
US $46.00 / mg 99.65% 10g TargetMol Chemicals Inc.
Diltiazem hydrochloride pictures 2024-11-19 Diltiazem hydrochloride
33286-22-5
US $46.00 / mg 99.65% 10g TargetMol Chemicals Inc.
diltiazem hydrochloride pictures 2024-11-18 diltiazem hydrochloride
33286-22-5
US $20.00 / kg 1kg 99.9% 10000 Hebei Miaoyin Technology Co.,Ltd

Diltiazem hydrochloride Spectrum

(2S-cis)-3-acetoxy-5-[2-(dimethylamino)ethyl]-2,3-dihydro-2-(4-methoxyphenyl)-1,5-benzothiazepin-4(5H)-one monohydrochloride 1,5-benzothiazepin-4(5h)-one,2,3-dihydro-3-(acetyloxy)-5-(2-(dimethylamino)eth 2,3-dihydro-3-(acetyloxy)-5-(2-(dimethylamino)ethyl)-2-(4-methoxyphenyl)-5-benzothiazepin-4(5h)-one altiazem anginyl angizem masdil monohydrochloride,cis-(+)-yl)-2-(4-methoxyphenyl) tildiem Adizem Zilde 1,5-Benzothiazepin-4(5H)-one, 3-(acetyloxy)-5-2-(dimethylamino)ethyl-2,3-dihydro-2-(4-methoxyphenyl)-, monohydrochloride, (2S,3S)- (+)-cis-diltiazem hydrochloride (2s,3s)-(+)-cis-3-acetoxy-5-(2-dimethylaminoethyl)-2,3-dihydro-2-(4-methoxyphenyl)-1,5-benzothiazepin-4(5h)-one hydrochloride DILTIAZEMHYDROCHLORIDE,USP (S,S)-Diltiazem hydrochloride 1,5-Benzothiazepin-4(5H)-one, 3-(acetyloxy)-5-[2-(dimethylamino)ethyl]-2,3-dihydro-2-(4-methoxyphenyl)-, monohydrochloride, (2S-cis)- Blocalcin 60 Cardizem CD Cardizem SR Citizem Cormax d-cis-3-Acetoxy-2,3-dihydro-5-[2-(dimethylamino)ethyl]-2-(p-methoxyphenyl)-1,5-benzothiazepin-4(5H)-one hydrochloride d-cis-Diltiazem hydrochloride Deltazen Dilacor Diladel Dilrene Dilzene Kardil RG 83606 Diltiazem HCl USP (+)-cis-3-(Acetyloxy)-5-(2-(dimethylamino)ethyl)-2,3-dihydro-2-(4-methoxyphenyl)-1,5-benzothiazepin-4(5H)one monohydrochloride Zilden 1,5-Benzothiazepin-4(5H)-one, 2,3-dihydro-3-(acetyloxy)-5-(2-(dimethylamino)ethyl)-2-(4- methoxyphenyl)-, monohydrochloride, cis-(+) Calnurs Clarute Cohlen Coroherser Diltiazem hydrochloride,99% CRD-401, (2S,3S)-(+)-cis-3-Acetoxy-5-(2-dimethylaminoethyl)-2,3-dihydro-2-(4-methoxyphenyl)-1,5-benzothiazepin-4(5H)-one hydrochloride (+)-cis-Diltiazem hydrochloride,(2S,3S)-(+)-cis-3-Acetoxy-5-(2-dimethylaminoethyl)-2,3-dihydro-2-(4-methoxyphenyl)-1,5-benzothiazepin-4(5H)-one hydrochloride, CRD-401 Diltiazem Hydrochloride (200 mg) Acetonitrile ( Test Diltiazem HCl, 1.0 mg/mL as free base) Dilthiazem hydrochlo Diltiazem HCl, (2S-cis)-3-(Acetyloxy)-5-[2-(dimethylamino)ethyl]-2,3-dihydro-2-(4-methoxyphenyl)-1,5-benzothiazepin-4(5H)-one hydrochloride Angipress (2S,3S)-(+)-CIS-3-(ACETOXY)-5-(2-DIMETHYLAMINOETHYL)-2,3-DIHYDRO-2-(4-METHOXYPHENYL)-1,5- 1,5-Benzothiazepin-4(5H)-one,3-(acetyloxy)-5-[2-(diMethylaMino)ethyl]-2,3-dihydro-2-(4-Methoxyphenyl)-,hydrochloride (1:1), (2S,3S)- RG 83606 HCl (2S,3S)- 3-(acetyloxy)-5-[2-(dimethylamino)ethyl]-2,3-dihydro-2-(4-methoxyphenyl)-1,5-benzothiazepin-4(5H)-one,hydrochloride (1:1) Diltiazem hydrochloride solution britiazim bruzem calcicard dilpral diltiazemchloridrate dilzem