트리부틸클로로실란

Tributylchlorosilane

HCID 70448CAS 995-45-9

기본 정보

표준 SMILES
CCCC[Si](Cl)(CCCC)CCCC
InChIKey
JSQJUDVTRRCSRU-UHFFFAOYSA-N
분자식
C12H27ClSi
평균 분자량
234.88 g/mol
단동위원소 질량
234.15705507

이름 및 식별자

우선 이름
Tributylchlorosilane
IUPAC
tributyl(chloro)silane
현지명
트리부틸클로로실란
영어명
Tributylchlorosilane
분자식
C12H27ClSi
분자량
234.88

이름 및 동의어

TributylchlorosilaneSilane, tributylchloro-EINECS 213-627-1NSC 139852DTXSID6061367RefChem:190914DTXCID7049130213-627-1JSQJUDVTRRCSRU-UHFFFAOYSA-N995-45-9Chlorotributylsilanetributyl(chloro)silane
이름 더 보기
트리부틸클로로실란DK963CHLOROTRI-N-BUTYLTributylchorosilanetributylchloro-silan
Chlorotri-n-butylsilaneTri-N-butylchlorosilaneTributylsilyl chlorideC12H27ClSiMFCD00000509tri-n-butylchlorosilane(chlorotri-n-butylsilane)CX2EDU6MJ7NSC-139852

데이터베이스 식별자

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

물성

구조 계산 물성

극성 표면적
0 Ų
수소 결합 공여자 수
0
수소 결합 수용자 수
0
회전 가능 결합 수
9
무거운 원자 수
14

물리화학적 성질

끓는 점
250 · 250-252 °C (lit.)
밀도
0.879 g/mL · 0.879 g/mL at 25 °C (lit.)
굴절률
20 · n20/D 1.446(lit.)
인화점
220 °F · 220 °F
저장 조건
Store at room temperature, keep dry and cool
물리적 상태
투명한 액체

안전 및 규제

GHS 분류

GHS Classification · 4건

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.

유해성 정보

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

안전 데이터

wgk
1
tsca
TSCA listed
ridadr
UN 2987 8/PG 2
HS 번호
29349990
risk_code
34-37
hazard_code
C

화학 및 산업

용도 및 제조

General Manufacturing InformationSilane, tributylchloro-: ACTIVE
응용 분야 · 3건

개요Tributylchlorosilane 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.

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

일반 설명Visit our Sensor Applications portal to learn more.

공급사50 곳

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]

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15건

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