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2,4,8,10-Tetraoxa-3,9-dithiaspiro[5.5]undecane 3,3,9,9-tetraoxide
[CAS# 201419-80-9]

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Complete supplier list of 2,4,8,10-Tetraoxa-3,9-dithiaspiro[5.5]undecane 3,3,9,9-tetraoxide
Identification
Classification Organic raw materials >> Organic sulfur compound
Name 2,4,8,10-Tetraoxa-3,9-dithiaspiro[5.5]undecane 3,3,9,9-tetraoxide
Molecular Structure CAS # 201419-80-9, 2,4,8,10-Tetraoxa-3,9-dithiaspiro[5.5]undecane 3,3,9,9-tetraoxide
Molecular Formula C5H8O8S2
Molecular Weight 260.24
CAS Registry Number 201419-80-9
EC Number 859-869-7
SMILES C1C2(COS(=O)(=O)O1)COS(=O)(=O)OC2
Properties
Solubility Sparingly soluble (12 g/L) (25 ºC), Calc.*
Density 1.86±0.1 g/cm3 (20 ºC 760 Torr), Calc.*
Index of Refraction 1.569, Calc.*
Boiling Point 480.7±45.0 ºC (760 mmHg), Calc.*
Flash Point 244.5±28.7 ºC, Calc.*
* Calculated using Advanced Chemistry Development (ACD/Labs) Software V11.02 (©1994-2019 ACD/Labs)
Safety Data
Hazard Symbols symbol symbol symbol symbol   GHS05;GHS06;GHS07;GHS08 Danger    Details
Hazard Statements H300-H302-H311-H317-H318-H330-H332-H340-H361fd-H372    Details
Precautionary Statements P203-P260-P261-P262-P264-P264+P265-P270-P271-P272-P280-P284-P301+P316-P301+P317-P302+P352-P304+P340-P305+P354+P338-P316-P317-P318-P319-P320-P321-P330-P333+P317-P361+P364-P362+P364-P403+P233-P405-P501    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Germ cell mutagenicityMuta.1BH340
Serious eye damageEye Dam.1H318
Acute toxicityAcute Tox.3H311
Acute toxicityAcute Tox.4H332
Acute toxicityAcute Tox.2H300
Skin sensitizationSkin Sens.1H317
Specific target organ toxicity - repeated exposureSTOT RE1H372
Reproductive toxicityRepr.2H361fd
Acute toxicityAcute Tox.4H302
Acute toxicityAcute Tox.2H330
up Discovory and Applicatios
2,4,8,10-Tetraoxa-3,9-dithiaspiro[5.5]undecane 3,3,9,9-tetraoxide, also known as Spiro-ATO, is a unique chemical compound that has garnered attention due to its distinctive structural features and its versatile applications, particularly in the field of polymer chemistry and as a precursor in organic synthesis. The compound is characterized by a spirocyclic framework, which is a rare and intriguing structure in organic chemistry, contributing to its stability and reactivity.

The discovery of 2,4,8,10-Tetraoxa-3,9-dithiaspiro[5.5]undecane 3,3,9,9-tetraoxide can be traced back to the exploration of sulfur-containing heterocycles in the mid-20th century. Researchers were particularly interested in these compounds due to their potential as intermediates in the synthesis of polymers and other complex organic molecules. The compound’s structure, which includes two sulfur atoms and multiple oxygen atoms arranged in a spirocyclic configuration, makes it highly reactive, especially in processes involving nucleophiles and electrophiles.

In terms of applications, Spiro-ATO has found significant use in the development of flame retardant materials. The presence of sulfur and oxygen in the compound's structure contributes to its ability to act as an effective flame retardant, particularly in polymeric materials. When incorporated into polymers, Spiro-ATO enhances their resistance to ignition and reduces the release of toxic gases during combustion. This makes it an ideal additive for polymers used in high-risk environments, such as in the construction and automotive industries, where fire resistance is critical.

Furthermore, Spiro-ATO has been utilized as a cross-linking agent in the production of thermosetting polymers. Its ability to form stable covalent bonds with various functional groups in polymer chains makes it valuable for creating materials with enhanced mechanical properties and chemical resistance. The cross-linked networks formed with Spiro-ATO exhibit superior durability, making them suitable for applications that require long-term stability under harsh conditions.

In addition to its use in polymers, Spiro-ATO has also been investigated as a precursor in the synthesis of other complex organic compounds. Its unique reactivity profile allows it to participate in a variety of chemical reactions, leading to the formation of products that are otherwise challenging to synthesize. This has led to its inclusion in research focused on the development of new materials, particularly in the field of medicinal chemistry where such compounds can serve as scaffolds for drug development.

The compound’s stability and reactivity have also made it a subject of interest in studies on environmentally friendly materials. Researchers are exploring its potential in creating sustainable polymers and additives that can replace more hazardous substances currently used in industry. Spiro-ATO's relatively benign environmental profile, coupled with its effectiveness, positions it as a promising candidate for green chemistry applications.

Overall, the discovery and application of 2,4,8,10-Tetraoxa-3,9-dithiaspiro[5.5]undecane 3,3,9,9-tetraoxide highlight the ongoing innovation in material science and organic synthesis. Its unique spirocyclic structure and versatility in various chemical processes make it a valuable compound in both industrial applications and academic research. As the demand for advanced materials continues to grow, Spiro-ATO is likely to play an increasingly important role in the development of new, high-performance, and environmentally sustainable materials.
Market Analysis Reports
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