24793-83-7

Basic information

• Product Name: 1-(4-methoxyphenyl)-2,2-dimethylpropane-1,3-diol
• CAS NO: 24793-83-7
• Molecular Formula: C₁₂H₁₈O₃
• Molecular Weight: 210.2695
• Mol File: 24793-83-7.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 359.6°C at 760 mmHg
• Flash Point: 171.3°C
• Density: 1.097g/cm³
• Vapor Pressure: 8.46E-06mmHg at 25°C
• Refractive Index: 1.532
• CAS DataBase Reference: 1-(4-methoxyphenyl)-2,2-dimethylpropane-1,3-diol(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-methoxyphenyl)-2,2-dimethylpropane-1,3-diol(24793-83-7)
• EPA Substance Registry System: 1-(4-methoxyphenyl)-2,2-dimethylpropane-1,3-diol(24793-83-7)

Safety Data

• Hazardous Substances Data: 24793-83-7(Hazardous Substances Data)

Usage

Description

1-(4-methoxyphenyl)-2,2-dimethylpropane-1,3-diol, also known as Bisabolol, is a chemical compound derived from the essential oil of chamomile. It is recognized for its anti-inflammatory, anti-irritant, and anti-microbial properties, which contribute to its wide range of applications across various industries.

Uses

Used in Cosmetic and Personal Care Industry:
1-(4-methoxyphenyl)-2,2-dimethylpropane-1,3-diol is used as an active ingredient for its soothing and skin-healing properties, making it ideal for products targeting sensitive or irritated skin.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 1-(4-methoxyphenyl)-2,2-dimethylpropane-1,3-diol is utilized as an anti-inflammatory agent, contributing to the effectiveness of medical ointments and related products.
Used in Fragrance Industry:
1-(4-methoxyphenyl)-2,2-dimethylpropane-1,3-diol is employed as a fragrance component for its pleasant, floral scent, enhancing the sensory experience of various products.
Overall, Bisabolol's safety and non-irritating nature render it a versatile compound suitable for a broad spectrum of applications in the cosmetic, pharmaceutical, and fragrance industries.

Upstream product

• 123-11-5 4-methoxy-benzaldehyde 
• 78-84-2 isobutyraldehyde 
• 64284-51-1 3-(4'-Methoxyphenyl)-3-hydroxy-2,2-dimethyl-propansaeure-ethylester 

Downstream Products

• 1354658-71-1 (R)-1-(4-methoxyphenyl)-5-phenylpentan-3-ol 
• 1181812-29-2 2,2-dimethyl-1-(4-methoxyphenyl)-1,3-propanediol 
• 602304-80-3 3-(4-methoxyphenyl)-2,2-dimethyl-3-oxopropan-1-yl 2,2-dimethylpropanoate 

Relevant articles and documents

Heterocyclization involving benzylic C(sp3)-H functionalization enabled by visible light photoredox catalysis

A general and efficient method for heterocyclization involving benzylic C(sp3)-H functionalization enabled by visible light photoredox catalysis to access a wide range of structurally diverse oxygen as well as nitrogen heterocycles up to a gram scale is reported. The potential application of this new methodology is demonstrated by the total synthesis of (-)-codonopsinine and (+)-centrolobine. Herein it is proposed that selectfluor, unlike a fluorinating reagent, acts as an oxidative quencher and a hydrogen radical acceptor.

Synthesis and biological activity of cis 2-(6-chloropyridine-3-yl) methylamino-4-substitutedphenyl-5,5-dimethyl-1,3,2-dioxaphosphinane 2-oxides

A series of novel, asymmetric-cyclic phosphoramides containing substituted pyridine were synthesized via the condensation reactions of trans 2-chloro-4-substitutedphenyl-5, 5-dimethyl-1,3,2-dioxaphosphinane 2-oxide with 2-chloro-5-aminomethylpyridine or 3

Fluoride-induced chemiluminescent decomposition of dioxetanes bearing a siloxyaryl moiety to produce an alkyl aryl ketone as an emitter

Tetrabutylammonium fluoride induces the decomposition of 1-tert-butyl-4,4-dimethyl-5-(3-siloxyphenyl)-2,6,7-trioxabicyclo[3.2.0] heptane (4a) in DMSO to form an oxyanion of aromatic ketone (14a) as an emitter with high singlet-chemiexcitation yield comparable with that for a chemically initiated electron exchange luminescence (CIEEL) active dioxetane producing an oxyanion of aromatic ester as an emitter. A 7-siloxynaphthalen-2-yl analog (4b) was found on similar treatment to emit light with the maximum wavelength the longest among CIEEL-active dioxetanes hitherto known.