18096-62-3

Basic information

• Product Name: INDOLAROME
• Synonyms: INDENO-M-DIOXIN TETRAHYDRO;INDOFLOR;INDOLAROME;2-d]-1,3-dioxin,4,4a,5,9b-tetrahydro-indeno[;2-d]-1,3-dioxin,4,4a,5,9b-tetrahydro-Indeno[1;4,4a,5,9b-tetrahydroindeno(1,2-d)-1,3-dioxin;4,5-Indeno-1,3-dioxan;1-Hydroxy-2-hydroxymethyl indan, methylene ether
• CAS NO: 18096-62-3
• Molecular Formula: C₁₁H₁₂O₂
• Molecular Weight: 176.21
• EINECS: 241-997-4
• Mol File: 18096-62-3.mol

Chemical Properties

• Boiling Point: 282.9°Cat760mmHg
• Flash Point: 131.4°C
• Appearance: /
• Density: 1.154g/cm³
• Vapor Pressure: 0.00557mmHg at 25°C
• Refractive Index: 1.554
• Water Solubility: 3.89g/L at 20℃
• CAS DataBase Reference: INDOLAROME(CAS DataBase Reference)
• NIST Chemistry Reference: INDOLAROME(18096-62-3)
• EPA Substance Registry System: INDOLAROME(18096-62-3)

Safety Data

• Hazardous Substances Data: 18096-62-3(Hazardous Substances Data)

Usage

Uses

Used in Perfumery Industry:
INDOLAROME is used as a fragrance ingredient for its indole-like odor, adding a distinct and pleasant scent to soaps and detergents. Its unique aroma makes it a valuable addition to the perfumer's palette, enhancing the overall sensory experience of these products.
Used in Soap and Detergent Manufacturing:
INDOLAROME is used as a scent enhancer in the production of soaps and detergents, providing a long-lasting and appealing fragrance to these cleaning products. Its incorporation into these products not only improves the user experience but also contributes to the overall effectiveness of the cleaning agents by attracting consumers through their sense of smell.

Flammability and Explosibility

Nonflammable

Trade name

Indoflor? (Symrise), Indolarome (IFF)

InChI:InChI=1/C11H12O2/c1-2-4-10-8(3-1)5-9-6-12-7-13-11(9)10/h1-4,9,11H,5-7H2

Upstream product

• 50-00-0 formaldehyd 
• 95-13-6 1-indene 

Downstream Products

• 5445-45-4 2-(hydroxymethyl)indan 

Relevant articles and documents

Highly efficient synthesis of 1,3-dioxanes via prins reaction in bronsted-acidic imidazolium ionic liquid

The high-yielding synthesis of a wide variety of 1,3-dioxanes via the Prins reaction under mild conditions has been demonstrated using Bronsted- acidic imidazolium ionic liquid [bmim(SO3H)][OTf] or bmimOTf. The use of ionic liquid makes this synthesis simple, convenient, cost-effective, and environmentally friendly. Furthermore, bmimOTf was conveniently separated from the products and can be easily recycled for the Prins reaction with excellent yields. This method works well with a variety of aliphatic aldehydes including formaldehyde, acetaldehyde, propionaldehyde, and cyclohexanecarboxaldehyde. [Supplementary materials are available for this article. Go to the publisher's online edition of Synthetic Communications for the following free supplemental resource(s): Full experimental and spectral details.]

Iodine as a mild and versatile reagent for the synthesis of 1,3-dioxane derivatives via the Prins reaction

Iodine is found to be an effective reagent for the cross-coupling of olefins with aldehydes under mild conditions to produce 4-substituted 1,3-dioxane derivatives in excellent yields and in short reaction times with high selectivity. The use of iodine makes this procedure simple, convenient, cost-effective and practical. This method works not only with formaldehyde but also with acetaldehyde, propionaldehyde and cyclohexanecarboxaldehyde.

Novel hydrophobic Bronsted acidic ionic-liquids as efficient and reusable catalysts for organic reactions in water

Novel Hydrophobic Bronsted acidic ionic liquids (HBAIL) were prepared and utilized as acid catalysts in organic reactions in water. HBAILs were demonstrated, for the first time, to be effective catalysts for Prins cyclization of styrene derivatives in water with a formaldehyde water solution. Many styrene derivatives could be successfully converted to the corresponding 1,3-dioxanes. Other dehydration reactions also proceeded well using HBAILs in water. After reactions, HBAILs could be easily recovered and reused without significant loss of activity. Copyright