Basic information
- Standard SMILES
C=C[Si](OCCOC)(OCCOC)OCCOC- InChIKey
WOXXJEVNDJOOLV-UHFFFAOYSA-N- Molecular formula
- C11H24O6Si
- Average molar mass
- 280.39 g/mol
- Monoisotopic mass
- 280.13421502
Names & identifiers
- Preferred name
- Tris(2-methoxyethoxy)vinylsilane
- IUPAC
- ethenyl-tris(2-methoxyethoxy)silane
- English name
- Vinyl tris(2-methoxyethoxy) silane
- Molecular formula
- C11H24O6Si
- Molecular weight
- 280.39
Names & synonyms
Show more names
Database identifiers
- CAS
1067-53-4- PubChem CID
- 14025
- DTXSID
DTXSID5027356- ChEMBL
CHEMBL1874769- UNII
- 907I50BC2S
- EC Number
- 213-934-0
- Nikkaji
- J150.388J
Properties
Computed structural properties
- Topological polar surface area
- 55.4 Ų
- Hydrogen bond donors
- 0
- Hydrogen bond acceptors
- 6
- Rotatable bonds
- 13
- Heavy atoms
- 18
- Formal charge
- 0
- Complexity
- 175
Experimental & physicochemical properties
Physicochemical properties
- Melting point
- -30 °C · -30 °C
- Boiling point
- 136.2 °C5.5 · 136.2 °C5.5 mm Hg(lit.)
- Density
- 1.034 g/mL · 1.034 g/mL at 25 °C(lit.)
- vapor pressure
- 0.017 · 0.017-1300Pa at 25℃
- refractive index
- 20 · n20/D 1.43(lit.)
- Flash point
- 230 °F · >230 °F
- storage temp.
- 2 · Sealed in dry,2-8°C
- solubility
- Chloroform (Slightly), Methanol (Slightly)
- form
- Liquid
- pka
- 10 · 10[at 20 ℃]
- color
- Colourless
- Specific Gravity
- 1.033 · 1.033
- Viscosity
- 1 · 1-2cs (25C)
- Water Solubility
- REACTS
- FreezingPoint
- -70 · < -70
- Hydrolytic Sensitivity
- 7 · 7: reacts slowly with moisture/water
- Sensitive
- Moisture Sensitive
- BRN
- 1795316 · 1795316
- Henry's Law Constant
- 5.9 · 5.9×102 mol/(m3Pa) at 25℃, Ebert et al. (2023)
- InChI
- 1S/C11H24O6Si/c1-5-18(15-9-6-12-2,16-10-7-13-3)17-11-8-14-4/h5H,1,6-11H2,2-4H3
- InChIKey
- WOXXJEVNDJOOLV-UHFFFAOYSA-N
- SMILES
- COCCO[Si](OCCOC)(OCCOC)C=C
- LogP
- -2 · -2-0.3 at 20℃
- Substances of Very High Concern (SVHC) Candidate List
- tris(2-methoxyethoxy)vinylsilane (1067-53-4)
- CAS DataBase Reference
- 1067 · 1067-53-4(CAS DataBase Reference)
- EWG's Food Scores
- 1 · 1
- FDA UNII
- 907 I50BC2S · 907I50BC2S
- NIST Chemistry Reference
- 2 · 2,5,7,10-Tetraoxa-6-silaundecane, 6-ethenyl-6-(2-methoxyethoxy)-(1067-53-4)
- EPA Substance Registry System
- 2 · 2,5,7,10-Tetraoxa-6-silaundecane, 6-ethenyl-6-(2-methoxyethoxy)- (1067-53-4)
- UNSPSC Code
- 12162002 · 12162002
- NACRES
- 23 · NA.23
- Symbol(GHS)
- 8 · GHS08
- Signal word
- Danger
- Hazard statements
- 360 FD · H360FD
- Precautionary statements
- 201 · P201-P202-P280-P308+P313-P405-P501
- PPE
- Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
- Hazard Codes
- Xn,T
- Risk Statements
- 21 · 21-36-62-61-20/21/22
- Safety Statements
- 26 · 26-36/37-53-45-36/37/39
- RIDADR
- 1993 · UN 1993
- WGK Germany
- 1 · 1
- RTECS
- 6826000 · VV6826000
- TSCA
- TSCA listed
- HazardClass
- 3.2 · 3.2
- PackingGroup
- III
- HS Code
- 29319090 · 29319090
- Storage Class
- 6.1 C · 6.1C - Combustible acute toxic Cat.3toxic compounds or compounds which causing chronic effects
- Hazard Classifications
- 1 B · Repr. 1B
- Toxicity
- 50 oral · LD50 oral in rat: 2960mg/kg
- REACH Registrations
- Active
Safety & regulation
GHS classification
GHS Classification
Danger
H360FD: May damage fertility; May damage the unborn child [Danger Reproductive toxicity]
P203, P280, P318, P405, and P501 (click each P-code to see the statement)
This chemical does not meet GHS hazard criteria for 2% (5 of 244) of reports.
Danger
H312 (28.7%): Harmful in contact with skin [Warning Acute toxicity, dermal]
Hazard information
Regulatory Information
Chemical: 2,5,7,10-Tetraoxa-6-silaundecane, 6-ethenyl-6-(2-methoxyethoxy)-
Hazard Traits - Reproductive Toxicity
2,5,7,10-Tetraoxa-6-silaundecane, 6-ethenyl-6-(2-methoxyethoxy)- is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of 2,5,7,10-Tetraoxa-6-silaundecane, 6-ethenyl-6-(2-methoxyethoxy)- are required to report information about their production and use of this chemical to the EPA under the Toxic Substances Control Act (TSCA). (40 eCFR Part 711)
Status: Active Update: 06-01-2022 https://echa.europa.eu/registration-dossier/-/registered-dossier/14177
Substance: tris(2-methoxyethoxy)vinylsilane
2,5,7,10-Tetraoxa-6-silaundecane, 6-ethenyl-6-(2-methoxyethoxy)-: Does not have an individual approval but may be used as a component in a product covered by a group standard. It is not approved for use as a chemical in its own right.
Hazard Classes and Categories
Acute Tox. 4 (28.7%)
Reproductive toxicity - category 1B
Flammable liquids - Category 4
Repr. 1B
Safety data
- PPE
- Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
- wgk
- 1
- tsca
- TSCA listed
- rtecs
- VV6826000
- ridadr
- UN 1993
- hs_code
- 29319090
- Toxicity
- LD50 oral in rat: 2960mg/kg
- risk_code
- 21-36-62-61-20/21/22
- Signal word
- Danger
- Symbol(GHS)
- GHS08
- hazard_code
- Xn,T
- safety_code
- 26-36/37-53-45-36/37/39
- hazard_class
- 3.2
- Storage Class
- 6.1C - Combustible acute toxic Cat.3toxic compounds or compounds which causing chronic effects
- packing_group
- III
- Hazard statements
- H360FD
- REACH Registrations
- Active
- Hazard Classifications
- Repr. 1B
- Precautionary statements
- P201-P202-P280-P308+P313-P405-P501
Chemistry & industry
Uses & manufacturing
General Manufacturing Information
Not Known or Reasonably Ascertainable
2,5,7,10-Tetraoxa-6-silaundecane, 6-ethenyl-6-(2-methoxyethoxy)-: ACTIVE
Applications
UsesA-172 is a bifunctional molecule that reacts with both inorganic fillers and organic polymers. It can be used as a binder accelerator for polymers filled with various minerals such as aluminum hydroxide, magnesium hydroxide, kaolin, and silica, improving their mechanical and electrical properties, especially after exposure to moisture. When combined with inorganic fillers, it hydrophobizes the filler surface, improving the compatibility between the filler and polymer, resulting in better dispersibility, lower melt viscosity, and easier processing of filled plastics.
DescriptionVinyltris(2-methoxyethoxy)silane is a vinyl-functional coupling agent that promotes adhesion among unsaturated, polyester-type resins or crosslinked polyethylene resins or elastomers and inorganic substrates, including fiber glass, silica, silicates and many metal oxides. When used as coupling agent, it reduces the sensitivity of the products’ mechanical and electrical properties to heat and/or moisture. Vinyl tris(2-methoxyethoxy) silane is mainly applied in these aspects: As an efficient adhesion promoter for various mineral-filled polymers, improving mechanical and electrical properties especially after exposure to moisture. A co-monomer for the preparation of different polymers such as polyethylene or acrylics. Those polymers show an improved adhesion to inorganic surfaces and they can also be crosslinked with moisture. Improving the compatibility of fillers with polymers, leading to a better dispersibility, reduced melt viscosity and easier processing of filled plastics. Pre-treating of glass, metals, or ceramic surfaces, improve the adhesion of coatings on these surfaces and corrosion resistance.
Upstream & downstream products
Upstream raw materials
Suppliers50 total
Related reactions
Linked notes
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