基本情報
- 標準SMILES
C=C[Si](C)(C)O[Si](C)(C)C=C- InChIKey
BITPLIXHRASDQB-UHFFFAOYSA-N- 分子式
- C8H18OSi2
- 平均分子量
- 186.4 g/mol
- 単同位体質量
- 186.08961826
名称と識別子
- 優先名称
- 1,3-Divinyltetramethyldisiloxane
- IUPAC
- ethenyl-[ethenyl(dimethyl)silyl]oxy-dimethylsilane
- 現地名
- 1,3-ジビニルテトラメチルジシロキサン
- 英語名
- Divinyltetramethyldisiloxane
- 分子式
- C8H18OSi2
- 分子量
- 186.4
名称と別名
名称をさらに表示
データベース識別子
- CAS
2627-95-4、68083-19-2- PubChem CID
- 75819
- DTXSID
DTXSID7038810- ChEMBL
CHEMBL1878672- UNII
- SJ4D71ZQF4
- EC Number
- 220-099-6
- Nikkaji
- J7.637F
物性
構造計算による物性
- 極性表面積
- 9.2 Ų
- 水素結合供与体数
- 0
- 水素結合受容体数
- 1
- 回転可能結合数
- 4
- 重原子数
- 11
- 形式電荷
- 0
- 複雑度
- 143
実験および物理化学的性質
Physical Description
Liquid
Colorless liquid; [Alfa Aesar MSDS]
物理化学的性質
- 融点
- -99 °C · -99 °C (lit.)
- 沸点
- 139 °C · 139 °C (lit.)
- 比重(密度)
- 0.809 g/mL · 0.809 g/mL at 25 °C (lit.)
- 蒸気圧
- 17 hPa · 17hPa at 25℃
- 屈折率
- 20 · n20/D 1.411(lit.)
- 闪点
- 76 °F · 76 °F
- 貯蔵温度
- Flammables area
- 外見
- 液体
- 比重
- 0.811 · 0.811
- 色
- 無色
- 水溶解度
- 不溶性
- BRN
- 1762585 · 1762585
- 化粧品成分の機能
- キレート化
- InChI
- 1S/C8H18OSi2/c1-7-10(3,4)9-11(5,6)8-2/h7-8H,1-2H2,3-6H3
- InChIKey
- BITPLIXHRASDQB-UHFFFAOYSA-N
- SMILES
- C[Si](C)(O[Si](C)(C)C=C)C=C
- LogP
- 5.4 at · 5.4 at 20℃
- CAS データベース
- 2627 · 2627-95-4(CAS DataBase Reference)
- NISTの化学物質情報
- 1 · Disiloxane, 1,3-diethenyl-1,1,3,3-tetramethyl-(2627-95-4)
- EPAの化学物質情報
- 1 · 1,3-Divinyl-1,1,3,3-tetramethyl disiloxane (2627-95-4)
化学的性質
化学的特性Colorless or yellowish transparent liquid
安全と法規制
GHS分類
GHS Classification
This chemical does not meet GHS hazard criteria for 0.4% (1 of 263) of reports.
Danger
H225 (94.3%): Highly Flammable liquid and vapor [Danger Flammable liquids]
P203, P210, P233, P240, P241, P242, P243, P261, P264, P264+P265, P271, P280, P302+P352, P303+P361+P353, P304+P340, P305+P351+P338, P318, P319, P321, P332+P317, P337+P317, P362+P364, P370+P378, P403+P233, P403+P235, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 263 reports by companies from 18 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
危険有害性情報
Regulatory Information
Chemical: Disiloxane, 1,3-diethenyl-1,1,3,3-tetramethyl-
Disiloxane, 1,3-diethenyl-1,1,3,3-tetramethyl- is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of Disiloxane, 1,3-diethenyl-1,1,3,3-tetramethyl- 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: 12-04-2023 https://echa.europa.eu/registration-dossier/-/registered-dossier/14606
Disiloxane, 1,3-diethenyl-1,1,3,3-tetramethyl-: 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.
毒性情報
安全データ
- F
- 10-21
- wgk
- 2
- tsca
- TSCA listed
- rtecs
- JM9235250
- ridadr
- UN 1993 3/PG 2
- hs_code
- 29319090
- risk_code
- 11-36/37/38-10
- 化審法
- (7)-483
- 消防法
- 危-4-2-III
- hazard_code
- F,Xi
- safety_code
- 16-26-36-37/39
- hazard_class
- 3
- packing_group
- III
- Hazard Classifications
- Flam. Liq. 2
- ストレージクラス
- 3 - Flammable liquids
化学と産業
用途と製造
General Manufacturing Information
All Other Chemical Product and Preparation Manufacturing
Disiloxane, 1,3-diethenyl-1,1,3,3-tetramethyl-: ACTIVE
応用分野
使用Divinyl tetramethyl disiloxane could be used as a additives(intermediates) in the production process of addition silicone rubber, silicone gel, liquid silicone, vinyl silicone resin, vinyl silicone oil, platinum chromium compound and others. POTENTIAL VINYL NUCLEOPHILE IN CROSS-COUPLING REACTIONS. 1,3-Divinyltetramethyldisiloxane acts as a potential vinyl donor used in cross-coupling reactions. It is also involved in the copolymerization reaction with aromatic ketones.
調製方法
製造方法The patent reports a method for preparing tetramethyldivinyldisiloxane, comprising the following steps: (1) mixing tetramethyldihydrogendisiloxane with a chloroplatinic acid catalyst to obtain a mixed solution; (2) bubbling acetylene into the mixed solution to carry out a hydrosilylation reaction, and after the reaction is completed, separating and purifying the reaction solution to obtain Divinyltetramethyldisiloxane.
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