Labetalol hydrochloride Chemical Properties

Melting point:

187-189°

storage temp. 

2-8°C

solubility 

H₂O: soluble

form 

powder

color 

white

Safety Information

Hazard Codes 

Xn

Risk Statements 

22

Safety Statements 

36

WGK Germany 

3

RTECS 

CV5376000

HS Code 

2924296000

Toxicity

LD50 in male, female mice, male, female rats (mg/kg): 114, 120, 113, 107 i.p.; 47, 54, 60, 53 i.v.; 1450, 1800, 4550, 4000 orally (Shimpo)

MSDS

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Labetalol hydrochloride Usage And Synthesis

Chemical Properties

White or almost white powder.

Originator

Trandate,Allen and Hanburys,UK,1977

Uses

tropane alkaloid, anticholinergic drug

Uses

vasoconstrictor

Definition

ChEBI: Labetalol hydrochloride is a member of salicylamides.

Manufacturing Process

(a) 5-Bromoacetylsalicylamide (2.6 g), N-benzyl-N-(1-methyl-3-phenylpropyl) amine (4.8 g) and methyl ethyl ketone (50 ml) were heated at reflux for 40 minutes. The solvent was removed and the residue was treated with benzene. The secondary amine hydrobromide was filtered off and discarded, and the filtrate was evaporated to dryness. The residue was treated with an excess of ethanolic hydrogen chloride when 5-[N-benzyl-N-(1-methyl-3-phenylpropyl)- glycyl]-salicylamide hydrochloride (1.15 g) crystallized out, MP 139°C to 141°C.
(b) 5-[N-benzyl-N-(1-methyl-3-phenylpropyl)glycyl]-salicylamide hydrochloride (0.75 g), 10% mixture of PdO and PtO on carbon catalyst (0.1 g) and ethanol (20 ml) were shaken at room temperature and pressure with hydrogen until uptake ceased. The catalyst was filtered off and the filtrate evaporated to dryness. The residue was crystallized from ethanol to give 5-[1- hydroxy-2-(1-methyl-3-phenylpropyl)aminoethyl]salicylamide hydrochloride as a white solid (0.40 g), MP 188°C.

brand name

Normodyne (Schering); Trandate (Promethus).

Therapeutic Function

Alpha-adrenergic blocker, Beta-adrenergic blocker

Biological Activity

labetalol hcl is a selective antagonist for the α1-adrenergic receptor and a non-selective antagonist for the β-adrenergic receptor. labetalol hcl has been used for the treatment of high blood pressure. labetalol hcl competitively targets the α1-adrenergic receptors expressed in vascular smooth muscle, thus inhibiting adrenergic stimulation on endothelial cells and vasoconstriction in peripheral blood vessels. labetalol hcl also blocks the β-adrenergic receptors in bronchial and vascular smooth muscle to counteract adrenergic stimulation. ultimately, labetalol hcl causes decreases in resting and exercise heart rates, cardiac output, as well as in both systolic and diastolic blood pressure, exherting vasodilation, as well as negative chronotropic and inotropic cardiac effects.1. national center for biotechnology information (2021). pubchem compound summary for cid 3869, labetalol. retrieved august 21, 2021.2. dage rc, hsieh cp. direct vasodilatation by labetalol in anaesthetized dogs. british journal of pharmacology, 1980, 70(2): 287-293.

Labetalol hydrochloride(32780-64-6)Related Product Information

• 5-acetyl-2-(phenylmethoxy)benzamide
• Labetalol IMpurity A
• Labetalol EP impurity D
• 5-formyl-2-hydroxybenzamide
• 5-(N,N-Dibenzylglycyl)salicylamide
• MDAT
• Labetalone hydrochloride
• DILEVALOL HYDROCHLORIDE
• Labetalol IMpurity B
• 5-(bromoacetyl)-2-(phenylmethoxy)benzamide
• (R)-N-benzyl-4-phenylbutan-2-amine
• Labetalol EP impurity C
• 5-(2-Bromo-1-hydroxyethyl)-2-hydroxy-benzoic Acid Methyl Ester
• Labetalol Hydrochloride Impurity 19（(R,S)-Labetalol Hydrochloride）
• rac 4-(3-Aminobutyl)phenol
• Salicylamide
• DILEVALOL
• SYNEPHRINE