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TRIMETHYLSILYL-MESO-INOSITOL is a synthetic chemical compound derived from inositol, a type of sugar alcohol. It is comprised of three methyl groups and one silyl group attached to the inositol molecule, which enhances its properties for various applications.

2582-79-8

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2582-79-8 Usage

Uses

Used in Analytical Chemistry:
TRIMETHYLSILYL-MESO-INOSITOL is used as a derivatization agent for improving the volatility and stability of analytes in gas chromatography-mass spectrometry analysis. This allows for more accurate and reliable detection and quantification of target compounds.
Used in Organic Synthesis:
In the field of organic synthesis, TRIMETHYLSILYL-MESO-INOSITOL serves as a precursor for the preparation of silyl ethers and esters. These silyl derivatives are valuable intermediates in the synthesis of various organic compounds.
Used in Pharmaceutical Industry:
TRIMETHYLSILYL-MESO-INOSITOL has potential applications in the pharmaceutical industry due to its ability to enhance the solubility and absorption of active ingredients. This can lead to improved bioavailability and therapeutic efficacy of drugs.
Used in Cosmetic Industry:
Similarly, in the cosmetic industry, TRIMETHYLSILYL-MESO-INOSITOL can be utilized to improve the solubility and absorption of active ingredients in cosmetic formulations, resulting in better performance and skin penetration of beneficial compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 2582-79-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,8 and 2 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2582-79:
(6*2)+(5*5)+(4*8)+(3*2)+(2*7)+(1*9)=98
98 % 10 = 8
So 2582-79-8 is a valid CAS Registry Number.
InChI:InChI=1/C24H60O6Si6/c1-31(2,3)25-19-20(26-32(4,5)6)22(28-34(10,11)12)24(30-36(16,17)18)23(29-35(13,14)15)21(19)27-33(7,8)9/h19-24H,1-18H3/t19-,20-,21-,22+,23-,24-

2582-79-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name trimethyl-[2,3,4,5,6-pentakis(trimethylsilyloxy)cyclohexyl]oxysilane

1.2 Other means of identification

Product number -
Other names Trimethylsilyl-meso-inositol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:2582-79-8 SDS

2582-79-8Downstream Products

2582-79-8Relevant academic research and scientific papers

Building blocks for oligospiroketal (OSK) rods and evaluation of their influence on rod rigidity

Wessig, Pablo,Moellnitz, Kristian

supporting information; experimental part, p. 3907 - 3920 (2012/06/30)

We report on the synthesis of three new sleeves and their incorporation in OSK rods. The structures of these sleeves are based on neo-inositol, terephthalaldehyde diacetals, and indacene. To quantify the influence of the sleeves on rod rigidity, we applied the worm-like chain (WLC) model on the new rods and found that this approach is rather disappointing. As the chief cause of this result, we assume that the rigidity of typical molecular rods largely exceeds the rigidity of polymers, which were successfully described by the WLC model. Alternatively, we suggest quantifying the rigidity of molecular rods by fitting an empirical function on the end-to-end distance distribution curve obtained by MD simulations. After checking various function types, the Levy-Martin function proved to be most suitable for this purpose. On the basis of this function, we defined the Levy-Martin parameter and suggest using this parameter for the characterization of the rigidity of molecular rods.

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