3047-10-7

Basic information

• Product Name: HEXA(CYCLOHEXYL)DITIN
• Synonyms: HEXA(CYCLOHEXYL)DITIN;HEXA(CYCOHEXYL)DITIN
• CAS NO: 3047-10-7
• Molecular Formula: C₃₆H₆₆Sn₂
• Molecular Weight: 736.33
• Mol File: 3047-10-7.mol

Chemical Properties

• Melting Point: >300°C
• Appearance: /
• CAS DataBase Reference: HEXA(CYCLOHEXYL)DITIN(CAS DataBase Reference)
• NIST Chemistry Reference: HEXA(CYCLOHEXYL)DITIN(3047-10-7)
• EPA Substance Registry System: HEXA(CYCLOHEXYL)DITIN(3047-10-7)

Safety Data

• TSCA: No
• Hazardous Substances Data: 3047-10-7(Hazardous Substances Data)

Usage

Uses

Used in Plastics Industry:
HEXA(CYCLOHEXYL)DITIN is used as a stabilizer and performance enhancer in the production of plastics. It helps to improve the durability, flexibility, and resistance to environmental factors, ensuring the longevity and quality of the final product.
Used in Rubber Industry:
In the rubber industry, HEXA(CYCLOHEXYL)DITIN serves as a crucial additive that enhances the elasticity, strength, and overall performance of rubber materials. Its incorporation into rubber formulations contributes to the creation of more reliable and durable rubber products.
Used in Adhesives Industry:
HEXA(CYCLOHEXYL)DITIN is used as a stabilizing agent in the production of adhesives, improving their bonding strength and resistance to various conditions. This results in more effective and long-lasting adhesives for a wide range of applications.
Used as a Stabilizer in Polyvinyl Chloride (PVC):
HEXA(CYCLOHEXYL)DITIN plays a significant role as a stabilizer in PVC, a widely used plastic material. It helps to prevent the degradation of PVC under heat and light exposure, ensuring the material's stability and maintaining its desirable properties.
Used in Fungicides:
This organotin compound is also utilized in some fungicides, where it exhibits antifungal properties. HEXA(CYCLOHEXYL)DITIN helps to protect crops and other plants from fungal infections, contributing to healthier and more productive agricultural yields.

InChI:InChI=1/6C6H11.2Sn/c6*1-2-4-6-5-3-1;;/h6*1H,2-6H2;;/r2C18H33Sn/c2*1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18/h2*16-18H,1-15H2

Upstream product

• 931-51-1 cyclohexylmagnesiumchloride 
• 3023-92-5 tris(cyclohexyl)tin bromide 
• 6056-50-4 tricyclohexyltin hydride 
• 1599-67-3 1-docosene 
• 7621-20-7 (cyclo-C₆H₁₁)3SnN(C₂H₅)2 
• 931-50-0 cyclohexylmagnesium bromide 

Downstream Products

• 20204-08-4 tris(cyclohexyl)(phenyl)stannane 

Relevant articles and documents

Synthesis and characterization of lipophilic organotins. Application to the functionalization of silica gel

The synthesis of the lipophilic docosyltri(hex-1-ynyl)tin was achieved in three steps according to two different synthetic pathways. This compound reacted with nonporous silica to yield surface-modified silica via the loss of the three alkynyl functionalities and the formation of Sibulk_O-Sn-C bonds. The reactivity and the maximum chain loading reached were compared to those obtained with the heptadecafluorodecyltin analogue. The differences observed were rationalized in terms of electronic demand and cross-sectional area of the grafted chain, as evidenced by FTIR spectroscopy and X-ray crystal structures of the precursors.