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1-(4-Methoxyphenoxy)-2-propanol, commonly known as guaifenesin, is a medication primarily used as an expectorant to facilitate the loosening of mucus in the airways, thereby making coughs more productive. It is a safe and well-tolerated over-the-counter remedy that works by increasing the volume and reducing the viscosity of respiratory secretions, easing the expulsion of mucus.

42900-54-9

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42900-54-9 Usage

Uses

Used in Pharmaceutical Industry:
1-(4-Methoxyphenoxy)-2-propanol is used as an expectorant for the relief of chest congestion and coughs caused by common cold, bronchitis, and other respiratory infections. It functions by enhancing the volume and decreasing the viscosity of secretions in the respiratory tract, making it easier for individuals to cough up mucus.
Available in various forms such as tablets, syrups, and liquids, guaifenesin is a widely accessible medication for respiratory relief. However, it is crucial to consult with a healthcare professional before use, particularly for those with specific medical conditions or who are taking other medications, to prevent potential side effects or interactions.

Check Digit Verification of cas no

The CAS Registry Mumber 42900-54-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,9,0 and 0 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 42900-54:
(7*4)+(6*2)+(5*9)+(4*0)+(3*0)+(2*5)+(1*4)=99
99 % 10 = 9
So 42900-54-9 is a valid CAS Registry Number.

42900-54-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-Methoxyphenoxy)-2-propanol

1.2 Other means of identification

Product number -
Other names 4-(2-Hydroxypropoxy)anisole

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:42900-54-9 SDS

42900-54-9Relevant academic research and scientific papers

Ruthenium-Catalyzed Selective Hydrogenation of Epoxides to Secondary Alcohols

Thiyagarajan, Subramanian,Gunanathan, Chidambaram

supporting information, p. 9774 - 9778 (2019/12/02)

A ruthenium(II)-catalyzed highly selective Markovnikov hydrogenation of terminal epoxides to secondary alcohols is reported. Diverse substitutions on the aryl ring of styrene oxides are tolerated. Benzylic, glycidyl, and aliphatic epoxides as well as diepoxides also underwent facile hydrogenation to provide secondary alcohols with exclusive selectivity. Metal-ligand cooperation-mediated ruthenium trans-dihydride formation and its reaction involving oxygen and the less substituted terminal carbon of the epoxide is envisaged for the origin of the observed selectivity.

Design, synthesis, and biological evaluation of new growth inhibitors of Trypanosoma cruzi (epimastigotes)

Schvartzapel, Andrea J.,Zhong, Li,Docampo, Roberto,Rodriguez, Juan B.,Gros, Eduardo G.

, p. 2314 - 2322 (2007/10/03)

As a continuation of our project aimed at the search for new chemotherapeutic agents against Chagas' disease, several drugs structurally related to the insect growth regulator Fenoxycarb and the naturally occurring juvenfie hormone of insects were designed, synthesized, and evaluated as antiproliferative agents against the parasite responsible of this disease. Isoprenoid derivatives (compounds 33, 34, 36, and 37) were potent growth inhibitors of Trypanosoma cruzi epimastigotes. In addition, taking into account the high activity observed for compound 30 and the inhibitory action of related compounds, the allyl ether moiety bonded at the polar extreme of these inhibitors proved to be a promising group for the design of new drugs.

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