トリブチルクロロシラン

Tributylchlorosilane

HCID 70448CAS 995-45-9

基本情報

標準SMILES
CCCC[Si](Cl)(CCCC)CCCC
InChIKey
JSQJUDVTRRCSRU-UHFFFAOYSA-N
分子式
C12H27ClSi
平均分子量
234.88 g/mol
単同位体質量
234.15705507

名称と識別子

優先名称
Tributylchlorosilane
IUPAC
tributyl(chloro)silane
現地名
トリブチルクロロシラン
英語名
Tributylchlorosilane
分子式
C12H27ClSi
分子量
234.88

名称と別名

TributylchlorosilaneSilane, tributylchloro-EINECS 213-627-1NSC 139852DTXSID6061367RefChem:190914DTXCID7049130213-627-1JSQJUDVTRRCSRU-UHFFFAOYSA-N995-45-9Chlorotributylsilanetributyl(chloro)silane
名称をさらに表示
トリブチルクロロシラントリ-N-ブチルクロロシラン(クロロトリ-N-ブチルシラン)クロロトリブチルシランDK963CHLOROTRI-N-BUTYLTributylchorosilanetributylchloro-silan
Chlorotri-n-butylsilaneTri-N-butylchlorosilaneTributylsilyl chlorideC12H27ClSiMFCD00000509tri-n-butylchlorosilane(chlorotri-n-butylsilane)CX2EDU6MJ7NSC-139852

データベース識別子

CAS
995-45-9
PubChem CID
70448
DTXSID
DTXSID6061367
UNII
CX2EDU6MJ7
EC Number
213-627-1
Nikkaji
J298.598E

物性

構造計算による物性

極性表面積
0 Ų
水素結合供与体数
0
水素結合受容体数
0
回転可能結合数
9
重原子数
14

物理化学的性質

沸点
250 · 250-252 °C (lit.)
比重(密度)
0.879 g/mL · 0.879 g/mL at 25 °C (lit.)
屈折率
20 · n20/D 1.446(lit.)
闪点
220 °F · 220 °F
貯蔵温度
Store at room temperature, keep dry and cool
外見
clear liquid

安全と法規制

GHS分類

GHS Classification · 4 件

Danger

H314 (100%): Causes severe skin burns and eye damage [Danger Skin corrosion/irritation]

P260, P264, P280, P301+P330+P331, P302+P361+P354, P304+P340, P305+P354+P338, P316, P321, P363, P405, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 45 reports by companies from 4 notifications to the ECHA C&L Inventory.

危険有害性情報

Hazard Classes and CategoriesSkin Corr. 1B (100%)

安全データ

F
10-21
wgk
1
tsca
TSCA listed
ridadr
UN 2987 8/PG 2
hs_code
29349990
risk_code
34-37

化学と産業

用途と製造

General Manufacturing InformationSilane, tributylchloro-: ACTIVE
応用分野 · 3 件

説明Tributylchlorosilane is a silanising agent widely used as a surface modification reagent and coupling agent in various chemical processes. It enhances hydrophobicity and improves adhesion properties by reacting with hydroxyl groups on surfaces to form stable siloxane bonds. Therefore, it is valuable in applications such as coating materials, silicone polymer manufacturing, and reagents for chromatographic analysis. The mechanism is that the chlorosilane group reacts with the surface hydroxyl group, replacing the surface chlorine atom by a covalent bond, while the butyl group provides hydrophobic properties.

使用Chlorotri-n-butylsilane is as silylating agent. It can react with bromo-trifluoro-methane, to product tributyl-trifluoromethyl-silane.

一般的な説明Visit our Sensor Applications portal to learn more.

調製方法

純化方法Fractionally distil it and store it in small aliquots in sealed ampoules. [Gilman et al. J Am Chem Soc 74 1361 1952, Osthoff & Clark J Org Chem 24 219 1959, Beilstein 4 IV 4072.]

サプライヤー50 社

苏州道澜生物医药科技有限公司15952404857 · [email protected]
上海阿拉丁生化科技股份有限公司400-6206333 13167063860 · [email protected]
Hebei Chuanghai Biotechnology Co., Ltd+86-17732866630 · [email protected]
上海麦克林生化科技股份有限公司021-50706066 15221275939 · [email protected]
武汉欣扬瑞和化学科技有限公司13720274133 · [email protected]

関連反応

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