3535-34-0

Basic information

• Product Name: 4-BUTOXY-3-METHOXY-BENZOIC ACID
• Synonyms: Albb-008962
• CAS NO: 3535-34-0
• Molecular Formula: C₁₂H₁₆O₄
• Molecular Weight: 224.26
• Mol File: 3535-34-0.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 344.2 °C at 760 mmHg
• Flash Point: 128 °C
• Appearance: /
• Density: 1.124 g/cm³
• Vapor Pressure: 2.56E-05mmHg at 25°C
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 4-BUTOXY-3-METHOXY-BENZOIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 4-BUTOXY-3-METHOXY-BENZOIC ACID(3535-34-0)
• EPA Substance Registry System: 4-BUTOXY-3-METHOXY-BENZOIC ACID(3535-34-0)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 3535-34-0(Hazardous Substances Data)

Usage

General Description

4-Butoxy-3-methoxy-benzoic acid, also known as p-butoxy-m-anisic acid, is a chemical compound with the molecular formula C12H16O4. It is an organic carboxylic acid that belongs to the class of benzoic acids. This chemical is commonly used as a UV filter in sunscreens and other cosmetics due to its ability to absorb and dissipate ultraviolet radiation. It also has potential pharmaceutical applications, particularly in the development of anti-inflammatory and analgesic drugs. Additionally, it is used in the manufacturing of dyes and pigments. 4-Butoxy-3-methoxy-benzoic acid may have potential environmental and health risks, as it can persist in the environment and may cause skin irritation or other adverse effects in high concentrations.

InChI:InChI=1/C12H16O4/c1-3-4-7-16-10-6-5-9(12(13)14)8-11(10)15-2/h5-6,8H,3-4,7H2,1-2H3,(H,13,14)/p-1

Upstream product

• 109-65-9 1-bromo-butane 
• 121-34-6 3-methoxy-4-hydroxybenzoic acid 
• 113628-75-4 4-butoxy-3-methoxy-benzoic acid methyl ester 
• 51301-87-2 4-butoxy-3-methoxybenzaldehyde 

Downstream Products

• 1123756-45-5 5-oxo-2,5-dihydrofuran-3-yl-4-butoxy-3-methoxybenzoate 
• 3535-43-1 4-n-butoxy-3-methoxybenzoil chloride 

Relevant articles and documents

Oxime Carbamate-Discovery of a series of novel FAAH inhibitors

A series of novel oxime carbamates have been identified as potent inhibitors of the key regulatory enzyme of the endocannabinoid signaling system, fatty acid amide hydrolase (FAAH). In this Letter, the rationale behind the discovery and the biological evaluations of this novel class of FAAH inhibitors are presented. Both in vitro and in vivo results of selected targets are discussed, along with inhibition kinetics and molecular modeling studies.1.

Substituted N-aryl heterocycles, process for their preparation and their use as medicaments

The invention relates to substituted N-aryl heterocycles and to the physiologically tolerated salts and physiologically functional derivatives thereof. Compounds of the formula I in which the radicals have the stated meanings, the N-oxides and the physiologically tolerated salts thereof and process for the preparation thereof are described. The compounds are suitable for example as anorectic agents.

Synthesis and biological activity of some 3,4-dialkoxy-substituted phenylethanolamines

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