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Guaifenesin

CAS No.
93-14-1
Chemical Name:
Guaifenesin
Synonyms
GLYCERYL GUAIACOLATE;GUAIPHENESIN;3-(2-methoxyphenoxy)propane-1,2-diol;gge;XL-90;Robitussin;RAC GUAIFENESIN;Glyceryl guaiacyl ether;GUAIACOL GLYCEROL ETHER;Glyceryl guaiacolate ether
CBNumber:
CB1743199
Molecular Formula:
C10H14O4
Molecular Weight:
198.22
MDL Number:
MFCD00016873
MOL File:
93-14-1.mol
MSDS File:
SDS
Last updated:2024-04-09 22:15:29

Guaifenesin Properties

Melting point 77-81 °C
Boiling point 215 °C (19 mmHg)
Density 1.1825 (rough estimate)
refractive index 1.5550 (estimate)
Flash point 215°C/19mm
storage temp. 2-8°C
solubility 50g/l (experimental)
pka 13.53±0.20(Predicted)
color White to Off-White
Water Solubility 5 g/100 mL (25 ºC)
Merck 14,4555
BRN 2049375
InChIKey HSRJKNPTNIJEKV-UHFFFAOYSA-N
LogP 1.390
CAS DataBase Reference 93-14-1(CAS DataBase Reference)
EWG's Food Scores 1-3
FDA UNII 495W7451VQ
ATC code R05CA03
NIST Chemistry Reference 3-(O-methoxyphenoxy)-1,2-propanediol(93-14-1)
EPA Substance Registry System Guaifenesin (93-14-1)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302
Precautionary statements  P264-P270-P301+P312-P501
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
Toxicity LD50 oral in rabbit: 2553mg/kg
NFPA 704
1
2 0

Guaifenesin price More Price(42)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich G5627 Guaiacol glyceryl ether ≥98% (GC) 93-14-1 25g $28.3 2024-03-01 Buy
Sigma-Aldrich 1301007 Guaifenesin United States Pharmacopeia (USP) Reference Standard 93-14-1 200mg $436 2024-03-01 Buy
TCI Chemical G0159 Guaiacol Glycerol Ether >98.0%(HPLC)(E) 93-14-1 25g $30 2024-03-01 Buy
TCI Chemical G0159 Guaiacol Glycerol Ether >98.0%(HPLC)(E) 93-14-1 500g $152 2024-03-01 Buy
Alfa Aesar A16827 3-(2-Methoxyphenoxy)-1,2-propanediol, 99+% 93-14-1 50g $31.65 2024-03-01 Buy
Product number Packaging Price Buy
G5627 25g $28.3 Buy
1301007 200mg $436 Buy
G0159 25g $30 Buy
G0159 500g $152 Buy
A16827 50g $31.65 Buy

Guaifenesin Chemical Properties,Uses,Production

Description

Guaifenesin 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. Additionally, Guaifenesin is also a centrally-acting muscle relaxant and is used routinely in combination with analgesics and sedatives in large-animal veterinary surgery.

Chemical Properties

This substance is a white crystalline powder with a melting point of 78.5-79°C and a boiling point of 215°C (2.53kPa). It is soluble in 20ml of water and ethanol, chloroform, glycerin, and dimethylformamide. It is easily soluble in benzene but insoluble in petroleum ether. It has a slightly bitter taste and a slightly particular odor.

Originator

GG Cen,Central,US,1975

History

Guaifenesin 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.

Uses

Guaifenesin is a muscle relaxant with expectorant properties often used as an expectorant to facilitate the removal of phlegm from the airways in acute respiratory tract infections. 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.

Definition

ChEBI: Guaifenesin is a member of methoxybenzenes.

Manufacturing Process

A 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 name

Mucinex (Adams).

General Description

Guaifenesin 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 action

Guaiphenesin facilitates secretion from bronchial mucous membranes, thus relieving a cough in colds, bronchitis, and bronchial asthma.

Synthesis

Guaiphenesin, 3-(o-methoxyphenoxy)-1,2-propandiol (23.2.3), is synthesized by reacting guiacol with 3-chloropropan-1,2-diol or with glycidol.

Synthesis_93-14-1

Veterinary Drugs and Treatments

In 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 Fate

Guaifenesin’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 evaluation

Guaifenesin 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.

References

[1] Peter V. Dicpinigaitis and Yvonne E. Gayle, Effect of Guaifenesin on Cough Reflex Sensitivity, 2003, vol. 124, 2178-2181 DOI:10.1378/CHEST.124.6.2178
[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 DOI:10.1016/j.pupt.2008.12.020
[3] Sittig's Pharmaceutical Manufacturing Encyclopedia
[4] Synthesis of Essential Drugs (2006, Elsevier)
[5] Plumb's Veterinary Drug Handbook
[6] https://pubchem.ncbi.nlm.nih.gov/compound/Guaifenesin

556-52-5
90-05-1
14007-09-1
93-14-1
Synthesis of Guaifenesin from Glycidol and Guaiacol
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View Lastest Price from Guaifenesin manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
guaifenesin pictures 2024-04-09 guaifenesin
93-14-1
US $0.00-0.00 / kg 1kg 99.99% 20 tons airuikechemical co., ltd.
Guaifenesin pictures 2024-01-02 Guaifenesin
93-14-1
US $55.00 / kg 10kg 0.99 20tons Zibo Hangyu Biotechnology Development Co., Ltd
POLYQUATERNIUM-37 pictures 2023-09-05 POLYQUATERNIUM-37
93-14-1
US $0.00 / KG 1KG 99% 50000KG/month Hebei Mojin Biotechnology Co., Ltd
  • guaifenesin pictures
  • guaifenesin
    93-14-1
  • US $0.00-0.00 / kg
  • 99.99%
  • airuikechemical co., ltd.
  • Guaifenesin pictures
  • Guaifenesin
    93-14-1
  • US $55.00 / kg
  • 0.99
  • Zibo Hangyu Biotechnology Development Co., Ltd
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 3-(o-Methoxyphenoxy)-propanediol-1,2 GUAIFENESIN /( )-3-(O-METHOXYPHENOXY)-1,2-PROPANEDIOL 3-(2-Methoxyphenoxy)-1,2-propanediol, erythro + threo, 99+% 3-o-Methoxyphenoxypropane 1:2-diol 3-o-methoxyphenoxypropane1:2-diol Aeronesin alpha-Glyceryl guaiacol ether alpha-Glyceryl guaiacolate ether alpha-glycerylguaiacolateether alpha-glycerylguaiacolether Aresol Breonesin Bronchol Calmipan component of Brondecon component of Colrex Expectorant component of Hycotuss component of Trind component of Trind-DM Cortussin Creson Dilyn Dorassin Flartussin G 87 g87 Gaiamar Glycerin guaiacolate Glycerin monoguaiacol ether glyceringuaiacolate glycerinmonoguaiacolether glycero-guaiacolether Glycerol alpha-(2-methoxyphenyl) ether Glycerol alpha-(o-methoxyphenyl)ether Glycerol alpha-guaiacyl ether Glycerol alpha-guiacyl ether Glycerol alpha-monoguaiacol ether Glycerol mono(2-methoxyphenyl) ether glycerolalpha-(2-methoxyphenyl)ether glycerolalpha-(o-methoxyphenyl)ether glycerolalpha-guaiacylether glycerol-alpha-guajakolether glycerol-alpha-monoguaiacolether glycerolmono(2-methoxyphenyl)ether Glyceryl guaiacol Glyceryl guaiacol ether Glyceryl guaicolate Glyceryl guiacolate glycerylguaiacol glycerylguaiacolateether