InChI Code for 3-Bis Hydroxypropyl Tetramethyldisiloxane

This article discusses the InChI code and the chemical formula for 3,3′-(1,1,3,3-Tetramethyldisiloxane-1,3-propan-1-ol). This chemical structure is presented in a three-dimensional visualization using a ball-and-stick model. The smaller the sphere, the clearer the view of the atoms and bonds. Interactive 3D visualization makes the chemical structure even clearer and easier to comprehend.

InChI code

The InChI code for 3-Bis hydratepropyl tetramethyldiloxane is a unique character string that represents the chemical substance. It was developed by the International Union of Pure and Applied Chemistry (IUPAC) Division VIII and is the standard for identifying chemical substances.

The IUPAC International Chemical Identifier is an international standard for molecular identifiers, which can be used in electronic and printed data sources. The InChI codes are managed by a subcommittee in IUPAC, which is a group of scientists and experts in the respective field.

The InChI identifier is a string of characters that describes a chemical substance. A chemical identifier includes atoms, chemical bonds, and tautomer information.

Other important information includes stereochemistry and electronic charge. There are 14 non-H bonds in the InChI code for 1,3-Bis(hydroxypropyl)tetramethyldisiloxane.

Chemical formula

This research shows the synthesis of 1-Bis-hydroxypropyl-tetramethyldisiloxan, or BHT, by using microwave irradiation. The resulting compound was investigated by means of nuclear magnetic resonance hydrogen spectroscopy and infrared spectroscopy.

Using the single factor method, an optimal reaction condition was identified, and a high yield of 83.9 percent was achieved. Additionally, the purity of the finished compound was 99.1%, making it one of the most pure and highly useful compounds.

Once you have the molecular formula of 3-Bis hydroxypropylesteredioxane, you can use the structure data file (SDF) to further investigate its chemical properties. The SDF file provides information about each atom, bond, and connectivity as well as its coordinates. This file can be imported into most chemistry-related software for three-dimensional visualization and further analysis.


This study presents a new method for the synthesis of 3,Bis-hydroxypropyl-tetramethyldisiloxan and reports on the characterization of the compound’s properties. The novel hydroxyester disiloxanes are prepared from the known monomers, triisobutylaluminum and tetraisobutylxane.

These compounds were further characterized by infrared spectroscopy and in the reaction process with diisocyanates. The results show that the synthesis process is a rapid and effective method of preparing this compound.

The tetraisobutylalumoxane reacts with diols to form oligomer compounds. The isobutyl radical is replaced, causing a molecular weight increase. The products are white glassy compounds with high solubility in benzene. The compounds synthesized from tetraisobutylalumoxane and g-diol do not dissolve in heptane, indicating that the oligomer may consist of oxyorganosiloxane fragments.


In this article, we discuss the methods of preparation of 3-Bis hydroxypropyl disiloxane. The basic steps are listed below. The catalyst is Lewissauren.

The first step is to mix the carboxylic acid unsaturated ester with dimethylchlorosilane. In the second step, an inert gas is added. The product of this step is hydrolyzed using Lewissauren.

Alternatively, the monomer may be hydrosilylated with an allylic cyclic siloxane. The latter is useful for dual-curable silicone compositions. The resulting cyclic siloxane polymer is either tetramethylcyclotetramethyldisiloxane (CAS:18001-97-3) or pentamethylcyclotetrasiloxane.


The chemical structure of 3,3′-(1,1,3,3)-Tetramethyldisiloxane-1,3-propan-1-ol can be deduced from its molecular formula. This structure includes 40 bond(s) with 14 non-H atoms, a carbon atom at the corner(s) and two primary alcohols.

A simulation of the reaction conditions revealed that the product ions were silanol-containing. Without such a property, the disiloxane ions lacked the hydrogen atom necessary for the product ions.

The result was a product ion that contained a hydrogen atom that is not labile. The structure of 3-Bis hydroxypropyl tetramethyldisiloxane can be visualized using the visualization tool.

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