Bis(triethoxysilylpropyl) disulfide CAS 56706-10-6

Introduction:Basic information about Bis(triethoxysilylpropyl) disulfide CAS 56706-10-6, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

Bis(triethoxysilylpropyl) disulfide Basic informationApplication

Product Name:Bis(triethoxysilylpropyl) disulfide
Synonyms:BIS(TRIETHOXYSILYLPROPYL)DISULFIDE;BIS[3-(TRIETHOXYSILYL)PROPYL]-DISULFIDE;4,4,13,13-tetraethoxy-3,14-dioxa-8,9-dithia-4,13-disilahexadecane;4,4,,-Tetraethoxy-3,-dioxa-8,9-dithia-4,-disilahexadecan;[Dithiobis(trimethylene)]bis(triethoxysilane);A-1589;Bis[3-(triethoxysilyl)propyl] perdisulfide;Bis[3-(triethoxysilyl)propyl] persulfide
CAS:56706-10-6
MF:C18H42O6S2Si2
MW:474.82
EINECS:260-350-7
Product Categories:silane;Adhesion Promoters;Coupling Agents;Dispersing Agents;Sulfur Silanes;Surface Modifiers;Industrial/Fine Chemicals;Sulfur
Mol File:56706-10-6.mol

Bis(triethoxysilylpropyl) disulfide Chemical Properties

Melting point °C
Boiling point 250
density 1.03
vapor pressure 0-7910Pa at 20-25℃
refractive index 1.457
Fp 75°C
storage temp. 2-8°C
Specific Gravity1.03
AppearanceColorless to light yellow Liquid
Water Solubility 14-1000000000μg/L at 20℃
Hydrolytic Sensitivity7: reacts slowly with moisture/water
InChIInChI=1S/C18H42O6S2Si2/c1-7-19-27(20-8-2,21-9-3)17-13-15-25-26-16-14-18-28(22-10-4,23-11-5)24-12-6/h7-18H2,1-6H3
InChIKeyFBBATURSCRIBHN-UHFFFAOYSA-N
SMILESCCO[Si](OCC)(OCC)CCCSSCCC[Si](OCC)(OCC)OCC
LogP-3-5.2 at 20℃
CAS DataBase Reference56706-10-6(CAS DataBase Reference)
EPA Substance Registry System3,14-Dioxa-8,9-dithia-4,13-disilahexadecane, 4,4,13,13-tetraethoxy- (56706-10-6)

Safety Information

Risk Statements 20/21/22-36/37/38
Safety Statements 26-36/37/39
TSCA TSCA listed

Bis(triethoxysilylpropyl) disulfide Usage And Synthesis

ApplicationFootwear
- Abrasion resistance
- Cutting and chunking resistance
- Flex life improvement
Rolls
- Abrasion resistance
- Aging resistance
- Processing- Set reduction (better load bearing)
- Reduced water swell
- Lower hysteresis
Mechanical Molded Goods
- Increased modulus
- Better heat aging
- Compression set reduction
- Dynamic property improvement
- Reduced swell to polar liquids
- Filler substitution (non-black for black)
Hose
- Improved abrasion on cover
- Better heat aging
- Increased modulus
- Lower compression set
- Improved adhesion to reinforcing elements
Solid Tires
- Improved abrasion
- Lower hysteresis
- Higher modulus
- Improved processing
- Possibly better adhesion
Tires
- Treads for abrasion, hot tear
- Carcass for adhesion and/or filler substitution
- Breaker (belt) stocks for adhesion
Belts
Flat Belts
- Increased abrasion
- Improved reversion resistance
- Reduced cost with clay substitution for black
- Improved cord adhesion
- Increased flex life and modulus
V Belts
- Increased modulus
- Improved abrasion
- Longer flex life
- Improved adhesion to reinforcing elements
Chemical PropertiesYellowish clear liquid
Flammability and ExplosibilityNot classified
Synthesis

5089-70-3

14814-09-6

60764-86-5

56706-10-6

General procedure for the synthesis of (3-mercaptopropyl)triethoxysilane (MPTES), compounds (CAS:60764-86-5) and bis-[3-(triethoxysilyl)propyl]-disulfide (TESPD) from 3-chloropropyltriethoxysilane (CPTES): during the reaction, 50 wt.% NaHSO4 was added drop-wise to a NaHS solution solution. 325 g (2.69 mol) of NaHS solution with 8.2 g (0.0124 mol) of tetrabutylammonium bromide (TBAB) solution were added to a glass reactor, mixed well and heated to 75 °C. Subsequently, NaHSO4 solution was added slowly and dropwise just before the imminent addition. Next, CPTES was added. 497.8 g (2.07 moles) of CPTES was added to the reaction mixture within 8 min. the addition of NaHSO4 solution needed to be completed within 30 min. After 5 hours of reaction, the organic phase was separated and analyzed by gas chromatography (GC). The analysis showed that the product contained 2.0% wt. of CPTES, 87.6% wt. of MPTES, 2.7% wt. of TESPM, and 0.7% wt. of TESPD.Finally, the product was distilled under vacuum to yield MPTES with a purity of 95.4%, which is about 84% yield based on the amount of CPTES used.

References[1] Patent: US6680398, 2004, B1. Location in patent: Page column 10-11
[2] Patent: US6680398, 2004, B1. Location in patent: Page column 8-9
[3] Patent: US6680398, 2004, B1. Location in patent: Page column 10
[4] Patent: US6680398, 2004, B1. Location in patent: Page column 9-10
[5] Patent: US6680398, 2004, B1. Location in patent: Page column 9

Bis(triethoxysilylpropyl) disulfide Preparation Products And Raw materials

Raw materials3-Chloropropyltriethoxysilane-->Sodium hydrosulfide-->Sodium bisulfate
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