14160-71-5

Basic information

• Product Name: 5-ETHOXYSALICYLIC ACID
• Synonyms: 5-ETHOXYSALICYLIC ACID;5-ETHOXY-2-HYDROXYBENZOIC ACID
• CAS NO: 14160-71-5
• Molecular Formula: C₉H₁₀O₄
• Molecular Weight: 182.17
• EINECS: 238-004-1
• Product Categories: Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts;C9;Carbonyl Compounds;Carboxylic Acids
• Mol File: 14160-71-5.mol

Chemical Properties

• Melting Point: 159-163 °C(lit.)
• Boiling Point: 354.1°Cat760mmHg
• Flash Point: 145.2°C
• Appearance: /
• Density: 1.292g/cm³
• Vapor Pressure: 1.26E-05mmHg at 25°C
• Refractive Index: 1.572
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 5-ETHOXYSALICYLIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 5-ETHOXYSALICYLIC ACID(14160-71-5)
• EPA Substance Registry System: 5-ETHOXYSALICYLIC ACID(14160-71-5)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36
• WGK Germany: 3
• Hazardous Substances Data: 14160-71-5(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
5-Ethoxysalicylic acid is used as an intermediate in the production of pharmaceuticals for its anti-inflammatory and antiseptic properties, making it a valuable component in the development of medications aimed at treating various conditions.
Used in Organic Synthesis:
In the field of organic chemistry, 5-Ethoxysalicylic acid serves as a key intermediate in the synthesis of other organic compounds, facilitating the creation of a wide array of chemical products.
Used in Topical Treatments for Skin Conditions:
Leveraging its anti-inflammatory and antiseptic properties, 5-Ethoxysalicylic acid is used as an active ingredient in topical treatments, providing relief and support for various skin conditions.
Used in Drug Therapy Development:
5-ETHOXYSALICYLIC ACID holds potential in the development of new drug therapies, where its unique properties can be harnessed to address specific medical needs or to enhance the effectiveness of existing treatments.
Used as a Reagent in Organic Chemistry Reactions:
5-Ethoxysalicylic acid also finds application as a reagent in various organic chemistry reactions, playing a crucial role in advancing chemical research and innovation.

InChI:InChI=1/C9H10O4/c1-2-13-6-3-4-8(10)7(5-6)9(11)12/h3-5,10H,2H2,1H3,(H,11,12)

Upstream product

• 74-96-4 ethyl bromide 
• 490-79-9 2,5-dihydroxybenzoic acid. 
• 75-03-6 ethyl iodide 
• 141-52-6 sodium ethanolate 

Downstream Products

• 14160-70-4 ethyl 5-ethoxy-2-hydroxybenzoate 
• 1383934-21-1 N-(4-chloro-3-(trifluoromethyl)phenyl)-2-(2-(dimethylamino)ethoxy)-5-ethoxybenzamide 
• 1383934-20-0 N-(4-chloro-3-(trifluoromethyl)phenyl)-5-ethoxy-2-hydroxybenzamide 
• 862845-77-0 3,3-diethoxy-6-oxo-N-phenylcyclohexa-1,4-dienecarboxamide 
• 862845-76-9 methyl 3,3-diethoxy-6-oxocyclohexa-1,4-dienecarboxylate 
• 862845-74-7 5-ethoxy-2-hydroxy-N-phenylbenzamide 
• 5315-78-6 methyl 5-ethoxy-2-hydroxybenzoate 

Relevant articles and documents

External preparation for skin

An external preparing for skin comprising one or more than two types of 2-hydroxy benzoic acid derivative and/or salt thereof represented by the following formula: STR1 wherein R is an alkoxy group or alkyl group in the formula. The external preparation for the skin according to the present invention has a suppression effect on melanine generation by inhibition of tyrosinase activity. Accordingly, an excellent bleaching effect based upon the suppression of chromatosis and a high degree of safety can be obtained.