Guaifenesin
Guaifenesin
  • CAS No.:93-14-1
Other grades of this product :
Guaifenesin Basic information
Description References
Product Name:Guaifenesin
Synonyms:1,2-Dihydroxy-3-(2-methoxyphenoxy)propane;1,2-Propanediol, 3-(2-methoxyphenoxy)-;1,2-Propanediol, 3-(o-methoxyphenoxy)-;2/G;2-G;3-(2-Methoxyphenosy)-1,2-propamediol;3-(2-methoxyphenoxy)-2-propanediol;3-(o-methoxyphenoxy)-2-propanediol
CAS:93-14-1
MF:C10H14O4
MW:198.22
EINECS:202-222-5
Product Categories:Building Blocks;C10;Chemical Synthesis;Ethers;Organic Building Blocks;Oxygen Compounds;Aromatics Compounds;Aromatics;Intermediates & Fine Chemicals;Pharmaceuticals;API's;Methocarbamol;API;MUCINEX;Benzhydrols, Benzyl & Special Alcohols
Mol File:93-14-1.mol
Guaifenesin Chemical Properties
Melting point 77-81 °C
Boiling point 215 °C (19 mmHg)
density 1.1825 (rough estimate)
refractive index 1.5550 (estimate)
Fp 215°C/19mm
storage temp. 2-8°C
solubility 50g/l (experimental)
form neat
pka13.53±0.20(Predicted)
color White to Off-White
Water Solubility 5 g/100 mL (25 ºC)
Merck 14,4555
BRN 2049375
InChIKeyHSRJKNPTNIJEKV-UHFFFAOYSA-N
CAS DataBase Reference93-14-1(CAS DataBase Reference)
NIST Chemistry Reference3-(O-methoxyphenoxy)-1,2-propanediol(93-14-1)
EPA Substance Registry SystemGuaifenesin (93-14-1)
Safety Information
Hazard Codes Xn
Risk Statements 22-36/37/38
Safety Statements 26-36
WGK Germany 1
RTECS TY8400000
Hazard Note Harmful
TSCA Yes
HS Code 29093090
Hazardous Substances Data93-14-1(Hazardous Substances Data)
ToxicityLD50 oral in rabbit: 2553mg/kg
MSDS Information
ProviderLanguage
ACROS English
SigmaAldrich English
ALFA English
Guaifenesin Usage And Synthesis
DescriptionGuaifenesin is an oral expectorant drug. The expectorant action of guaifenesin is mediated by stimulation of the gastrointestinal tract. It is a common ingredient in prescription and over-the-counter medications used to treat cough due to colds and minor upper respiratory infections.
References[1] Peter V. Dicpinigaitis and Yvonne E. Gayle, Effect of Guaifenesin on Cough Reflex Sensitivity, 2003, vol. 124, 2178-2181 [2] Leonid Kagan, Eran Lavy and Ammon Hoffmann, Effect of mode of administration on guaifenesin pharmacokinetics and expectorant action in the rat model, Pulmonary Pharmacology & Therapeutics, 2009, vol. 22, 260-265
DescriptionGuaifenesin was originally derived from the guaiac tree and used by Native Americans for health purposes. Synthesis of guaifenesin was first reported in 1912. Guaifenesin has been used in the treatment of respiratory diseases since the nineteenth century. The United States’ Food and Drug Administration (FDA) approved guaifenesin for use in overthe- counter medications in 1989. Guaifenesin is widely consumed alone and combined with antihistamines, cough suppressants, and decongestants. Guaifenesin is also a centrally acting muscle relaxant and is used routinely in combination with analgesics and sedatives in large-animal veterinary surgery.
Chemical PropertiesWhite Solid
OriginatorGG Cen,Central,US,1975
UsesCentrally acting muscle relaxant with expectorant properties
UsesUsed to assist the expectoration of phlegm from the airways in acute respiratory tract infections.
UsesGuaifenesin is commonly used as an expectorant. Guaifenesin comes in tablet and capsule form, as syrup, as dissolving granules, and recently as an extended-release (longacting) tablet. The tablets, capsules, dissolving granules, and syrup are usually taken with or without food every 4 h as needed. The extended-release tablet is usually taken with or without food every 12 h. In veterinary medicine, guaifenesin is given intravenously to induce muscle relaxation when administering anesthesia. It relaxes both laryngeal and pharyngeal muscles, allowing easier intubation. Guaifenesin is also used in the treatment of horses with exertional rhabdomyolysis and in dogs with strychnine intoxication.
Manufacturing ProcessA mixture of o-methoxyphenol (57 g), glycidol (32 g) and pyridine (1 g) is warmed to 95°C at which temperature a vigorous reaction takes place. The reaction mixture is cooled to prevent the temperature rising above 110°C. When the exothermic reaction has subsided the reactants are heated at 95°C for one hour longer and then distilled under low pressure. The main fraction boils in the range 176°C to 180°C/0.5 mm. It crystallizes on cooling. Recrystallization from benzene gives the pure product, MP 78.5°C to 79.0°C.
Brand nameMucinex (Adams).
Therapeutic FunctionExpectorant
General DescriptionGuaifenesin is an expectorant, widely used in the treatment of cough. Its mode of action involves the alleviating of cough discomfort by increasing sputum volume and decreasing its viscosity, thus resulting in effective cough.Pharmaceutical secondary standards for application in quality control, provide pharma laboratories and manufacturers with a convenient and cost-effective alternative to the preparation of in-house working standards.
Mechanism of actionGuaiphenesin facilitates secretion from bronchial mucous membranes, thus relieving a cough in colds, bronchitis, and bronchial asthma.
SynthesisGuaiphenesin, 3-(o-methoxyphenoxy)-1,2-propandiol (23.2.3), is synthesized by reacting guiacol with 3-chloropropan-1,2-diol or with glycidol.
Veterinary Drugs and TreatmentsIn veterinary medicine, guaifenesin is used to induce muscle relaxation and restraint as an adjunct to anesthesia for short procedures (30 – 60 minutes) in large and small animal species. There are combination oral products containing guaifenesin for treating respiratory conditions in horses. In human medicine, guaifenesin has long been touted as an oral expectorant, but definitive proof of its efficacy is lacking.
Environmental FateGuaifenesin’s production and use as veterinary and human medicines may result in its release to the environment through various waste streams. If released to air, an estimated vapor pressure of 1.5× 10–6 mm Hg at 25 ℃ indicates that guaifenesin will exist in both the vapor and particulate phase. Based upon an estimated Henry’s law constant of 4.4 × 10-11 atm-m3 mol-1, volatilization from moist soil surfaces or from water surfaces are not expected to be important fate processes for guaifenesin. Guaifenesin is expected to have high mobility in soil based upon an organic carbon–water partition coefficient (Koc) of 140, which indicates that it will have more solubility in water and is less likely to adsorb onto organic matter in soil and plants.
Toxicity evaluationGuaifenesin is an adrenergic antagonist in a class of medications called expectorants. It stimulates afferent receptors in the gastric mucosa, reflexively increasing glandular secretion by the respiratory epithelium promoting lower respiratory tract drainage by thinning bronchial secretions, lubricating irritated respiratory tract membranes through increased mucous flow, and facilitating removal of viscous mucus. The onset of action appears to be within 15–30 min. Guaifenesin is believed to alleviate cough discomfort by improving sinus and bronchial drainage, increasing sputum volume, and decreasing sputum viscosity, thereby promoting effective cough. In one study, the effect of guaifenesin to increase mucociliary clearance from the lung was greater in patients with chronic bronchitis than in healthy subjects. In another study, guaifenesin inhibited the cough reflex sensitivity in subjects with an upper respiratory tract infection (cough receptors are transiently hypersensitive), but not in healthy volunteers. Possible mechanisms include a central antitussive effect or a peripheral effect by increased sputum volume serving as a physical barrier, shielding cough receptors within the respiratory epithelium. As a centrally acting muscle relaxant, guaifenesin is believed to depress or block nerve impulse transmission at the internuncial neuron level of the subcortical areas of the brain, brain stem, and spinal cord. It also has mild analgesic and sedative actions.
Guaifenesin Preparation Products And Raw materials
Raw materialsAmmonium hydroxide-->Diethyl carbonate-->Guaiacol-->3-Chloro-1,2-propanediol-->Glycidol
Preparation ProductsZinc oxide-->Lithopone-->Zinc nitrate hexahydrate-->Methocarbamol-->2-METHOXYPHENOXYACETIC ACID

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