Ranitidine Hydrochloride Chemical Properties

Melting point:

134°C (dec.)

storage temp. 

2-8°C

solubility 

H₂O: 1.8 mg/mL

form 

solid

color 

tan

Water Solubility 

Soluble in water, 2-hydroxypropyl-beta-cyclodextrin, acetic acid, methanol, ethanol and dimethyl sulfoxide. Insoluble in chloroform.

Sensitive 

Hygroscopic

Merck 

14,8110

BCS Class

3/1

Stability:

Hygroscopic

CAS DataBase Reference

66357-59-3(CAS DataBase Reference)

Safety Information

Hazard Codes 

F,T

Risk Statements 

20/21/22-39/23/24/25-23/24/25-11

Safety Statements 

22-24/25-45-36/37-16-7

WGK Germany 

2

RTECS 

KM6557000

HS Code 

2932190002

MSDS

• Language:English Provider:SigmaAldrich
• Language:English Provider:ALFA

Ranitidine Hydrochloride Usage And Synthesis

Background and overview

Ranitidine Hydrochloride (RHCl) is a kind of histamine H2 receptor antagonist. Since its listing in 1981, ranitidine hydrochloride has been widely used in nearly one hundred countries in the world, including China. It is clinically used for the treatment of duodenal ulcer, reflux esophagitis and Zollinger-Ellison syndrome. It is also used for the prevention of gastrointestinal bleeding caused by stress ulcer and recurrent hemorrhage of peptic ulcer. In recent decade, through the combination of ranitidine and other drugs, it has found that it has high efficiency and remarkable features in the treatment of Helicobacter pylori-positive duodenal ulcer, urticaria and post-cerebral hemorrhage stress ulcer with better efficacy than other similar drugs. Owing to its rapid effect, good potency and low price, ranitidine hydrochloride plays an important role in the anti-ulcer drug market today. Therefore, strict quality control plays important roles in guiding patients with reasonable, safe medication.

Pharmacological effects

This product is a H2 receptor inhibitor, being capable of inhibiting the gastric acid secretion. After oral administration, it is absorbed through the gastrointestinal tract quickly. Synthetic route [4]
The intermediates (3) and (5) were synthesized as follows. The intermediates (3) and (5) were then reacted to produce (6) ranitidine. The (6) is subject to purification and salt formation to generate ranitidine hydrochloride, as shown:

Pharmacokinetics

After oral administration, it is absorbed rapidly from the gastrointestinal tract with a bioavailability (F) of about 50% and peak plasma concentration (tmax) reaching within 1 to 2 hours. Plasma protein binding rate is 15% ± 3%; effective blood concentration is 100ng / ml, widely distributed in the body with the apparent volume of distribution (Vd) of 1.1 ~ 1.9L / Kg. It can penetrate through the blood brain barrier with the drug concentration in cerebrospinal fluid being 1/30 ~ 1 / 20 of blood concentration. 30% is subject to liver metabolism with the metabolites including N-oxide, S-oxide and demethylation metabolites. 50% of the prototype is subject to urine excretion through kidney. Half-life (t1 / 2) is 2 to 3 hours, which is similar to cimetidine. Renal failure causes corresponding increase in the half-life. The goods can be transplanted via the placenta with the milk concentration being higher than the plasma concentration of drugs.

Indications

For the treatment of duodenal ulcer, gastric ulcer, reflux esophagitis, Zollinger-Ellison syndrome and other high acid secretion disorders.

Adverse reactions

• Common reactions are: nausea, rash, constipation, fatigue, headache, dizziness and so on.
• Light adverse reactions on the renal function, gonadal function and central nervous system.
• A small number of patients get mild liver damage after taking the drug with the symptoms disappearing after stopping, liver function returned to normal.

Medicine interactions

• Combination with procainamide reduces the clearance rate of the later one.
• Drug interactions may occur if used with other medications, consult physician or pharmacist for details.

Precautions

• This product mustn’t be used continuously for more than 7 days, the symptom is not relieved, consult your physician or pharmacist.
• Elderly patients or patients with liver and kidney dysfunction use with caution.
• If overdose or serious adverse reactions, should seek medical treatment immediately.
• Disable it for people who are allergic to this product; allergies should use with caution.
• This product is not allowed for administration upon change of its traits.
• Please put this product where children cannot touch.
• Children must be under adult guardianship. 
• If you are using other drugs, please consult your physician or pharmacist before using this product.

Contraindication

• Children under 8 years should be disabled.
• Pregnant and lactating women should be disabled.

Elderly patients medication

The elderly have reduced liver and kidney function; in order to ensure drug safety, dosage should be adjusted.

Chemical Properties

Off-White Crystalline Solid

Uses

A histamine H2-receptor antagonist which inhibits gastric acid secretion. Antiulcerative.

Uses

antifungal

Uses

An H-2 histamine receptor antagonistRanitidine hydrochloride is mainly used as an H2-receptor antagonist and helps in the treatment of gastrointestinal lesions because of excessive gastric acid secretion. It also serves as an antiulcer drug.

brand name

Zantac (GlaxoSmithKline).

Biological Activity

ranitidine is a histamine h2-receptor antagonist that inhibits stomach acid production.ranitidine (zantac) is a histamine h2-receptor antagonist with ic50 of 3.3 ± 1.4 um. it inhibits stomach acid production. it is also used alongside fexofenadine and oth

Biochem/physiol Actions

H2 histamine receptor antagonist; anti-ulcer agent.

Contact allergens

Ranitidine, an H2-receptor antagonist, can cause contact dermatitis within the pharmaceutical industry and in health care workers, or may induce systemic drug reactions in patients.

storage

+4°C (desiccate)

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