β1 receptor blocker Uses Hazards & Safety Information
ChemicalBook > CAS DataBase List > Metoprolol tartrate

Metoprolol tartrate

β1 receptor blocker Uses Hazards & Safety Information
Product Name
Metoprolol tartrate
CAS No.
56392-17-7
Chemical Name
Metoprolol tartrate
Synonyms
beloc;h93/26;Prelis;Niflam;betaloc;seloken;Metapro;Sipseron;lopresor;Selopral
CBNumber
CB7436617
Molecular Formula
2C15H25NO3.C4H6O6
Formula Weight
684.82
MOL File
56392-17-7.mol
More
Less

Metoprolol tartrate Property

Melting point:
120℃
Boiling point:
695.37°C (rough estimate)
Density 
1.1946 (rough estimate)
refractive index 
1.5300 (estimate)
Flash point:
9℃
storage temp. 
2-8°C
solubility 
H2O: soluble50mg/mL
form 
powder
color 
white to off-white
Water Solubility 
Soluble in water (>1000 mg/ml), methanol (>500 mg/ml), chloroform (496 mg/ml), ethanol (31 mg/ml at 25°C), and DMSO (100 mg/ml at 25°C).
λmax
223nm(H2O)(lit.)
Merck 
14,6151
BCS Class
1
Stability:
Stable. Incompatible with strong oxidizing agents.
CAS DataBase Reference
56392-17-7(CAS DataBase Reference)
More
Less

Safety

Hazard Codes 
F,T
Risk Statements 
11-23/24/25-39/23/24/25
Safety Statements 
7-16-36/37-45-24/25
RIDADR 
UN1230 - class 3 - PG 2 - Methanol, solution
WGK Germany 
3
RTECS 
UB7450100
HS Code 
29225090
Toxicity
LD50 in female mice, male rats (mg/kg): 118, ~90 i.v.; 2090, 3090 orally (Bodin)
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H411Toxic to aquatic life with long lasting effects

Precautionary statements

P201Obtain special instructions before use.

P202Do not handle until all safety precautions have been read and understood.

P273Avoid release to the environment.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P308+P313IF exposed or concerned: Get medical advice/attention.

P391Collect spillage. Hazardous to the aquatic environment

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
M-123
Product name
Metoprolol tartrate solution
Purity
1.0?mg/mL in methanol (as free base), ampule of 1?mL, certified reference material, Cerilliant?
Packaging
1mL
Price
$36.6
Updated
2024/03/01
Sigma-Aldrich
Product number
BP540
Product name
Metoprolol tartrate
Purity
British Pharmacopoeia (BP) Reference Standard
Packaging
100MG
Price
$233
Updated
2024/03/01
Sigma-Aldrich
Product number
1441301
Product name
Metoprolol tartrate
Purity
United States Pharmacopeia (USP) Reference Standard
Packaging
200mg
Price
$436
Updated
2024/03/01
Sigma-Aldrich
Product number
80337
Product name
(±)-Metoprolol (+)-tartrate salt
Purity
analytical standard
Packaging
100mg
Price
$58.6
Updated
2022/05/15
Alfa Aesar
Product number
J61920
Product name
Metoprolol tartrate, 98+%
Packaging
5g
Price
$78.5
Updated
2024/03/01
More
Less

Metoprolol tartrate Chemical Properties,Usage,Production

β1 receptor blocker

Metoprolol tartrate is a selective β1-adrenergic receptor blocker,oral absorption is rapid  and complete,it is used for the treatment of hypertension, angina pectoris, myocardial infarction, hypertrophic cardiomyopathy, aortic dissection, cardiac arrhythmia, hyperthyroidism, cardiac neurosis and other diseases. In recent years, it is also used for ther treatment of heart failure, which can reduce mortality. In unstable/non-ST-segment elevation myocardial infarction and acute myocardial infarction  control guiding principles developed by American Heart Association , effect of metoprolol tartrateare is clearly recognized. In the past, concerns about β-blocker therapy caused hypotension is too large, and for the consideration that there may be racial differences between Asians in β-blocker use and the West, patients with treatment of β-blockers in China is  fewer  , the use of β-blockers is in lower dose.
Metoprolol tartrate has a weaker membrane stability and it has no intrinsic sympathomimetic activity, and in comparison with similar drugs commonly used in clinical propranolol ,in addition to the advantages of β1-blocker on its pharmacodynamic,it also has its pharmacokinetic kinetics  advantages, such as relatively weak first-pass effect compared with propranolol, simple metabolic pathways, most pharmacologically inactive metabolites and the like.

Uses

Hypertensive medication.

Hazards & Safety Information

Category: toxic substances
Toxicity grading: Middle  poisoning
Acute toxicity: oral -rat LD50: 5500 mg/kg; Oral-Mouse LD50: 1500 mg/kg
Flammability and hazard characteristics: It is combustible; fire decomposition produces toxic nitrogen oxide gases
Storage Characteristics: Ventilated, low-temperature ,dry storeroom.
Extinguishing agent: Water, carbon dioxide, dry powder, sandy soil.

Description

Metoprolol (tartrate) (Item No. 21165) is an analytical reference standard categorized as a β1-adrenergic receptor blocker. This product is intended for use in analytical forensic applications. Metoprolol (succinate) is available as a general research tool .

Chemical Properties

White or almost white, crystalline powder or colourless crystals.

Originator

Betaloc,Astra,UK,1975

Uses

Metoprolol tartrate is an antagonist of the β1-AR (β1-adrenoceptor). It inhibits spontaneous endothelin-1 production in vitro and displays antihypertensive and antianginal activity in vivo.

Uses

A ? selective aryloxypropanolamine andrenergic antagonist. Used in the treatment of a variety of cardiovascular disorder. Antihypertensive; antianginal; antiarrhythmic (class II)

Uses

A β1 selective aryloxypropanolamine andrenergic antagonist. Used in the treatment of a variety of cardiovascular disorder. Antihypertensive; antianginal; antiarrhythmic (class II).

Uses

alpha(1)-adrenergic blocker

Uses

A b1-Adrenergic blocker

Manufacturing Process

The starting material 1,2-epoxy-3-[p-(β-methoxyethyl)phenoxy]-propane was obtained from p-(β-methoxyethyl)-phenol which was reacted with epichlorohydrin whereafter the reaction product was distilled at 118°C to 128°C at a pressure of 0.35mm Hg.
1,2-Epoxy-3-[p-(β-methoxyethyl)-phenoxy]-propane (16.7g) was dissolved in 50 ml isopropanol and mixed with 20 ml isopropylamine. The mixture was heated in an autoclave on boiling water-bath overnight, whereafter it was evaporated and the remainder dissolved in 2 N HCI. The solution was extracted first with ether and thereafter with methylene chloride. After evaporating the methylene chloride phase, the hydrochloride of 1- isopropylamino-3-[p(β-methoxyethyl)-phenoxy] -propanol-2 was obtained which, after recrystallization from ethyl acetate, weighed 10.4 g. Melting point 83°C. Equivalent weight: found 304.0, calculated 303.8.
The hydrochloride is then converted to the tartrate.

brand name

Lopressor (Novartis).

Therapeutic Function

Beta-adrenergic blocker

General Description

A certified solution standard applicable for use in clinical toxicology or forensic analysis by LC-MS/MS or GC/MS. Metoprolol is used for the treatment of multiple heart conditions including hypertension, angina, and tachycardia. This beta blocker is sold under the trade names Lepressor and Toprol XL?.

Biological Activity

Selective β 1 -adrenoceptor antagonist (K i values are 47, 2960 and 10100 nM for β 1 , β 2 and β 3 adrenoceptors respectively). Inhibits spontaneous endothelin-1 production in vitro and displays antihypertensive and antianginal activity in vivo .

Clinical Use

Beta-adrenoceptor blocker:
Hypertension
Angina
Cardiac arrhythmias
Migraine prophylaxis
Hyperthyroidism

Veterinary Drugs and Treatments

Because metoprolol is relatively safe to use in animals with bronchospastic disease, it is often chosen over propranolol. It may be effective in supraventricular tachyarrhythmias, premature ventricular contractions (PVC’s, VPC’s), systemic hypertension, and treating cats with hypertrophic cardiomyopathy. There is increasing interest in using beta blockers in heart failure in dogs; one retrospective study showed increased survival times when dogs were given metoprolol, but definitive prospective, double-blinded studies have not been reported documenting the benefit (increased survival) of beta-blockers in dogs with heart failure.

Drug interactions

Potentially hazardous interactions with other drugs
Anaesthetics: enhanced hypotensive effect.
Analgesics: NSAIDs antagonise hypotensive effect.
Anti-arrhythmics: increased risk of myocardial depression and bradycardia; increased risk of bradycardia, myocardial depression and AV block with amiodarone; increased risk of myocardial depression and bradycardia with flecainide; concentration increased by propafenone and dronedarone.
Antibacterials: concentration reduced by rifampicin.
Antidepressants: enhanced hypotensive effect with MAOIs; concentration increased by citalopram and escitalopram and possibly by paroxetine - avoid.
Antihypertensives; enhanced hypotensive effect; increased risk of withdrawal hypertension with clonidine; increased risk of first dose hypotensive effect with post-synaptic alpha-blockers such as prazosin.
Antimalarials: increased risk of bradycardia with mefloquine; avoid with artemether/lumefantrine.
Antipsychotics enhanced hypotensive effect with phenothiazines.
Antivirals: avoid concomitant use with tipranavir in heart failure.
Calcium-channel blockers: increased risk of bradycardia and AV block with diltiazem; hypotension and heart failure possible with nifedipine and nisoldipine; asystole, severe hypotension and heart failure with verapamil.
Cytotoxics: possible increased risk of bradycardia with crizotinib.
Diuretics: enhanced hypotensive effect.
Fingolimod: possibly increased risk of bradycardia.
Moxisylyte: possible severe postural hypotension.

Metabolism

Extensively metabolised in the liver, mainly by the cytochrome P450 isoenzyme CYP2D6, and undergoes oxidative deamination, O-dealkylation followed by oxidation, and aliphatic hydroxylation. The metabolites are excreted in the urine with only small amounts of unchanged metoprolol.

storage

Desiccate at RT

Metoprolol tartrate Preparation Products And Raw materials

Raw materials

Preparation Products

More
Less

Metoprolol tartrate Suppliers

Jai Radhe Sales
Tel
+(91)-(79)-26431096/65255722
Fax
+(91)-(79)-26569884
Email
info@jairadhesales.com
Country
India
ProdList
397
Advantage
60
TCI Chemicals (India) Pvt. Ltd.
Tel
--
Fax
--
Email
sales-in@tcichemicals.com
Country
India
ProdList
6768
Advantage
58
Jigs Chemical Limited
Tel
--
Fax
--
Email
info@jigschemical.com
Country
India
ProdList
235
Advantage
58
Triveni chemicals
Tel
--
Fax
--
Email
sales@trivenichemical.com
Country
India
ProdList
6088
Advantage
58
Arnav Pharma Chem
Tel
--
Fax
--
Email
apc@arnavpharmachem.com
Country
India
ProdList
57
Advantage
58
Innorex Pharmaceuticals Private Limited
Tel
--
Fax
--
Email
info@innorexpharma.com
Country
India
ProdList
173
Advantage
58
Sangeeta Pharma
Tel
--
Fax
--
Country
India
ProdList
21
Advantage
58
Omicron Pharma
Tel
--
Fax
--
Email
info@omicronpharma.in
Country
India
ProdList
11
Advantage
58
Luconic Chemicals
Tel
--
Fax
--
Country
India
ProdList
72
Advantage
58
Esschem Pvt., Ltd.
Tel
--
Fax
--
Email
esschem@vsnl.com
Country
India
ProdList
96
Advantage
58
Oceanic Pharmachem Pvt., Ltd. (OPPL)
Tel
--
Fax
--
Email
info@oceanicpharmachem.com
Country
India
ProdList
946
Advantage
58
Moksha Lifesciences
Tel
--
Fax
--
Email
sales@mokshapharma.com
Country
India
ProdList
51
Advantage
58
Clearsynth Labs
Tel
--
Fax
--
Email
fo@clearsynth.com
Country
India
ProdList
3887
Advantage
58
Pharma Links
Tel
--
Fax
--
Email
info@pharmalinksindia.com
Country
India
ProdList
85
Advantage
58
Royal Trading Corporation
Tel
--
Fax
--
Country
India
ProdList
135
Advantage
58
Viraj Pharmaceuticals Pvt. Ltd.
Tel
--
Fax
--
Email
virajppl@gmail.com
Country
India
ProdList
162
Advantage
58
Aril Pharmaceuticals (Aril Biosciences Pvt. Ltd.)
Tel
--
Fax
--
Email
marketing@arilpharmaceuticals.com
Country
India
ProdList
67
Advantage
58
Vitalchemie Exim Pvt., Ltd.
Tel
--
Fax
--
Email
enquiries@vitalchemie.com
Country
India
ProdList
85
Advantage
58
Aadivighnesh Chem Private Ltd.
Tel
--
Fax
--
Email
sales@aadivighnesh.com
Country
India
ProdList
119
Advantage
58
ITM Chem ( India ) Pvt., Ltd.
Tel
--
Fax
--
Country
India
ProdList
35
Advantage
58
Polydrug Laboratories Pvt. Ltd.
Tel
--
Fax
--
Email
polydrug@polydrug.com
Country
India
ProdList
131
Advantage
58
Rashtriya chemicals Corporation.
Tel
--
Fax
--
Country
India
ProdList
13
Advantage
58
Metro Exporters Pvt. Ltd.
Tel
--
Fax
--
Email
metro@metroexporters.net
Country
India
ProdList
204
Advantage
58
Atman Pharmaceuticals
Tel
--
Fax
--
Email
atman.parekh@atman.net.in
Country
India
ProdList
55
Advantage
58
Vervain Pharm Chem
Tel
--
Fax
--
Email
export@vervain.co.in
Country
India
ProdList
139
Advantage
58
Parshwanath Life Science
Tel
--
Fax
--
Email
parshwanath2424@yahoo.co.in
Country
India
ProdList
5
Advantage
58
International Drug & Chemical Co.
Tel
--
Fax
--
Email
sales@idcco.com
Country
India
ProdList
65
Advantage
58
Sun Pharmaceutical Industries Ltd.
Tel
--
Fax
--
Email
SunPharma.IndiaBusiness@sunpharma.com
Country
India
ProdList
99
Advantage
58
SPB Pharma Chiemimpex
Tel
--
Fax
--
Email
sales@spbpharmachem.com
Country
India
ProdList
94
Advantage
58
Griffith Overseas Pvt. Ltd.
Tel
--
Fax
--
Email
sourcing@griffithoverseas.com
Country
India
ProdList
46
Advantage
58
Pharma Chemicals
Tel
--
Fax
--
Country
India
ProdList
130
Advantage
58
Mehta Associates
Tel
--
Fax
--
Email
info@mehtaassociates.co.in
Country
India
ProdList
17
Advantage
58
McCoy Drugs Pvt. Ltd.
Tel
--
Fax
--
Email
mccoydrugs@hotmail.com
Country
India
ProdList
21
Advantage
58
Reine Lifescience
Tel
--
Fax
--
Email
reinelifescience@gmail.com
Country
India
ProdList
4
Advantage
58
BCM Corporation
Tel
--
Fax
--
Email
sales@bcmcorporation.com
Country
India
ProdList
57
Advantage
58
Raisa Pharmachem Inds.
Tel
--
Fax
--
Email
raisa@bom5.vsnl.net.in
Country
India
ProdList
38
Advantage
58
Nivon Specialties (India)
Tel
--
Fax
--
Email
info@nivonindia.com
Country
India
ProdList
154
Advantage
58
Unimax Chemicals Pvt. Ltd.
Tel
--
Fax
--
Email
info@unimax.co.in
Country
India
ProdList
39
Advantage
58
Gemini Exports
Tel
--
Fax
--
Email
uiry@geminiexpor
Country
India
ProdList
140
Advantage
58
Ebenezer Industries
Tel
--
Fax
--
Email
info@ebenezerindia.in
Country
India
ProdList
53
Advantage
58
Abil Chempharma Pvt. Ltd.
Tel
--
Fax
--
Email
exports@abilchempharma.in
Country
India
ProdList
38
Advantage
58
Medkem Laboratories
Tel
--
Fax
--
Email
info@medkem.com
Country
India
ProdList
295
Advantage
58
Ipca Laboratories Ltd.
Tel
--
Fax
--
Email
manas.gorani@ipca.com
Country
India
ProdList
75
Advantage
58
B. Shah & Sons
Tel
--
Fax
--
Country
India
ProdList
79
Advantage
58
Livealth Biopharma Private Limited
Tel
--
Fax
--
Email
sales@livealthbiopharma.in
Country
India
ProdList
27
Advantage
58
ALEMBIC PHARMACEUTICALS LIMITED
Tel
--
Fax
--
Email
infoal@alembic.co.in
Country
India
ProdList
62
Advantage
58
Rawia International HealthCare Pvt. Ltd.
Tel
--
Fax
--
Email
info@rawia.in
Country
India
ProdList
170
Advantage
58
Ayon PharmaChem
Tel
--
Fax
--
Email
bhargav@ayonpharmachem.com
Country
India
ProdList
303
Advantage
58
Prachi Pharmaceuticals Pvt., Ltd.
Tel
--
Fax
--
Email
info@prachipharmaceuticals.com
Country
India
ProdList
26
Advantage
58
Afton Pharma
Tel
--
Fax
--
Email
info@aftonpharma.com
Country
India
ProdList
40
Advantage
58
More
Less

View Lastest Price from Metoprolol tartrate manufacturers

WUHAN FORTUNA CHEMICAL CO., LTD
Product
Metoprolol tartrate 56392-17-7
Price
US $0.00/KG
Min. Order
1KG
Purity
98%min
Supply Ability
30tons/month
Release date
2023-02-08
Hebei Mingeng Biotechnology Co., Ltd
Product
Metoprolol Tartrate 56392-17-7
Price
US $200.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
1000kg/Month
Release date
2022-11-25
Shijiazhuang Gantuo Biotechnology Co., Ltd
Product
Metoprolol Tartrate 56392-17-7
Price
US $100.00/mg
Min. Order
25mg
Purity
99%
Supply Ability
1000g
Release date
2023-03-10

56392-17-7, Metoprolol tartrateRelated Search:


  • Metoprolol tar
  • 1-[4-(2-methoxyethyl)phenoxy]-3-[(1-methylethyl)amino]-2-propanol, (2R,3R)-2,3-dihydroxybutanedioate (2:1)
  • Metoprolol tartrate solution
  • 2-Propanol, 1-4-(2-methoxyethyl)phenoxy-3-(1-methylethyl)amino-, (2R,3R)-2,3-dihydroxybutanedioate (2:1) (salt)
  • (±)1-(isopropylamino)-3-[p-(β-methoxyethyl)phenoxy]-2-propanol tartrate salt
  • METOPROLOLTARTRATE,USP
  • METOPROLOE TARTRATE
  • (+-)-1-(Isopropylamino)-3-[4-(2-methoxyethyl)phenoxy]-2-propanol tartrate
  • (+-)-Metoprolol bitartrate
  • 1-(Isopropylamino)-3-[4-(2-methoxyethyl)phenoxy]-2-propanol tartrate
  • 2-Propanol, 1-[4-(2-methoxyethyl)phenoxy]-3-[(1-methylethyl)amino]-, (+-)-, [R-(R*,R*)]-2,3-dihydroxybutanedioate (2:1) (salt)
  • 2-Propanol, 1-[4-(2-methoxyethyl)phenoxy]-3-[(1-methylethyl)amino]-, (2R,3R)-2,3-dihydroxybutanedioate (2:1) (salt) (9CI)
  • 2-Propanol, 1-[4-(2-methoxyethyl)phenoxy]-3-[(1-methylethyl)amino]-, [R-(R*,R*)]-2,3-dihydroxybutanedioate (2:1) (salt)
  • CGP 2175E
  • HCTCGP 2175E
  • Vasocardin
  • Lopressor, (±)1-(Isopropylamino)-3-[p-(β-methoxyethyl)phenoxy]-2-propanol (+)-tartrate salt
  • 2-Propanol, 1-[4-(2-methoxyethyl)phenoxy]-3-[(1-methylethyl)amino]-, (2R,3R)-2,3-dihydroxybutanedioate (2:1)
  • Metoproferm
  • (±)1-(Isopropylamino)-3-[p-(beta-methoxyethyl)phenoxy]-2-propanol tartrate (2:1) salt
  • Cerekunart
  • Kokonalin
  • Sipseron
  • Zegumular
  • Metoprolol Tartrate (200 mg)
  • (±)-Metoprolol (+)-tartrate salt,(±)1-(Isopropylamino)-3-[p-(β-methoxyethyl)phenoxy]-2-propanol (+)-tartrate salt, Lopressor
  • (±)-Metoprolol (+)-t
  • (±)1-(Isopropylamino)-3-[p-(β-methoxyethyl)phenoxy]-2-propanol tartrate salt Lopressor
  • Metoprolol tartrate, >=99%
  • 1-(Isopropylamino)-3-(4-(2-methoxyethyl)phenoxy)propan-2-ol hemi((2R,3R)-2,3-dihydroxysuccinate)
  • Metoprolol Tartrat
  • (±)1-(Isopropylamino)-3-[p-(β-methoxyethyl)phenoxy]-2-propanol tartrate salt Lopressor 1-(Isopropylamino)-3-(p-(2-methoxyethyl)phenoxy)-2-propanol (2:1) Dextro-tartrate salt
  • artrate(2:1)
  • beloc
  • betaloc
  • h93/26
  • lopresor
  • lopressor
  • metoprololhemitartrate
  • metoprololtartrate(2:1)
  • seloken
  • slowlopresor
  • METOPROLOL TARTARIC ACID
  • METOPROLOL TARTRATE
  • (+/-)-METOPROLOL (+)-TARTRATE SALT
  • (+-)-1-(isopropylamino)-3-(p-(2-methoxyethyl)phenoxy)-2-propanolhemi-l-tartr
  • (+-)-1-(isopropylamino)-3-(p-(2-methoxyethyl)phenoxy)-2-propanoltartrate(2:
  • 1-(4-(2-methoxyethyl)phenoxy)-3-((1-methylethyl)amino)-2-propano(+-)-2-propanot
  • 1-(isopropylamino)-3-(p-(2-methoxyethyl)phenoxy)-2-propano(+-)-2-propanotartrate
  • 1-(isopropylamino)-3-(p-(2-methoxyethyl)phenoxy)-2-propanol (2:1) dextro-tartrate salt
  • 1-[ISOPROPYLAMINO]-3-[P-(BETA-METHOXY-ETHYL)PHENOXY]-2-PROPANOL(+)-TARTRATE SALT
  • METOPROLOL TARTRATE CRYSTALLINE POWDER
  • 1-[4-(2-Methoxyethyl)phenoxy]-3-[(1-methylethyl)amino]-2-propanol Hemi (+)-Tartrate
  • Lapressor
  • Prelis
  • rac Metoprolol Hemi (+)-Tartrate
  • Selopral
  • 1-(isopropylaMino)-3-(4-(2-Methoxyethyl)phenoxy)propan-2-ol (2R,3R)-2,3-dihydroxysuccinate