0-sec-부틸페놀

0-sec-부틸페놀
0-sec-부틸페놀 구조식 이미지
카스 번호:
89-72-5
한글명:
0-sec-부틸페놀
동의어(한글):
0-sec-부틸페놀;오쏘-이차-부틸페놀;2-(1-메틸프로필)페놀
상품명:
2-sec-Butylphenol
동의어(영문):
OSBP;O-S-BUTYLPHENOL;2-sec.Butylfenol;O-SEC-BUTYLPHENOL;2-SEC-BUTYLPHENOL;2-(2-butyl)phenol;o-sec-butyl-pheno;2-sek.Butylphenol;0-sec-butylphenol;Phenol,o-sec-butyl-
CBNumber:
CB4734578
분자식:
C10H14O
포뮬러 무게:
150.22
MOL 파일:
89-72-5.mol
MSDS 파일:
SDS

0-sec-부틸페놀 속성

녹는점
12 °C(lit.)
끓는 점
226-228 °C(lit.)
밀도
0.982 g/mL at 25 °C(lit.)
증기압
0.03 mm Hg ( 20 °C)
굴절률
n20/D 1.522(lit.)
인화점
234 °F
산도 계수 (pKa)
10.36±0.35(Predicted)
물리적 상태
액체
색상
흰색에서 밝은 노란색
수용성
불용성. 20°C에서 <0.1g/100mL
BRN
1210026
노출 한도
ACGIH: TWA 5 ppm (Skin)
NIOSH: TWA 5 ppm(30 mg/m3)
안정성
안정적이지만 공기에 민감합니다. 산 염화물, 산 무수물, 염기, 강산화제, 구리 및 그 합금, 황동과 호환되지 않습니다.
LogP
3 at 20℃
CAS 데이터베이스
89-72-5(CAS DataBase Reference)
NIST
Phenol, 2-(1-methylpropyl)-(89-72-5)
EPA
o-sec-Butylphenol (89-72-5)
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
위험품 표기 C
위험 카페고리 넘버 20/21/22-34-22
안전지침서 26-27-28-36/37/39-45
유엔번호(UN No.) UN 3145 8/PG 2
WGK 독일 2
RTECS 번호 SJ8920000
TSCA Yes
위험 등급 8
포장분류 III
HS 번호 29071910
유해 물질 데이터 89-72-5(Hazardous Substances Data)
기존화학 물질 KE-25306
그림문자(GHS): GHS hazard pictogramsGHS hazard pictograms
신호 어: Danger
유해·위험 문구:
암호 유해·위험 문구 위험 등급 범주 신호 어 그림 문자 P- 코드
H302 삼키면 유해함 급성 독성 물질 - 경구 구분 4 경고 GHS hazard pictograms P264, P270, P301+P312, P330, P501
H314 피부에 심한 화상과 눈에 손상을 일으킴 피부부식성 또는 자극성물질 구분 1A, B, C 위험 GHS hazard pictograms P260,P264, P280, P301+P330+ P331,P303+P361+P353, P363, P304+P340,P310, P321, P305+ P351+P338, P405,P501
예방조치문구:
P270 이 제품을 사용할 때에는 먹거나, 마시거나 흡연하지 마시오.
P280 보호장갑/보호의/보안경/안면보호구를 착용하시오.
P301+P312 삼켜서 불편함을 느끼면 의료기관(의사)의 진찰을 받으시오.
P303+P361+P353 피부(또는 머리카락)에 묻으면 오염된 모든 의복은 벗거나 제거하시오 피부를 물로 씻으시오/샤워하시오.
P305+P351+P338 눈에 묻으면 몇 분간 물로 조심해서 씻으시오. 가능하면 콘택트렌즈를 제거하시오. 계속 씻으시오.
NFPA 704
1
3 0

0-sec-부틸페놀 MSDS


2-sec-Butylphenol

0-sec-부틸페놀 C화학적 특성, 용도, 생산

화학적 성질

colourless to light yellow liquid

용도

Chemical intermediate in preparation of resins, plasticizers, surface-active agents.

정의

ChEBI: A member of the class of phenols that is phenol carrying a butan-2-yl group at position 2.

일반 설명

Clear colorless liquid.

공기와 물의 반응

Insoluble in water.

반응 프로필

Phenols, such as 2-sec-Butylphenol, do not behave as organic alcohols, as one might guess from the presence of a hydroxyl (-OH) group in their structure. Instead, they react as weak organic acids. Phenols and cresols are much weaker as acids than common carboxylic acids (phenol has Ka = 1.3 x 10^[-10]). These materials are incompatible with strong reducing substances such as hydrides, nitrides, alkali metals, and sulfides. Flammable gas (H2) is often generated, and the heat of the reaction may ignite the gas. Heat is also generated by the acid-base reaction between phenols and bases. Such heating may initiate polymerization of the organic compound. Phenols are sulfonated very readily (for example, by concentrated sulfuric acid at room temperature). The reactions generate heat. Phenols are also nitrated very rapidly, even by dilute nitric acid.

위험도

Skin, eye, and upper respiratory tract irri- tant.

건강위험

o-sec-Butylphenol is a skin, eye, and respiratory irritant.
Acute occupational exposures have resulted in mild respiratory irritation as well as skin burns.

화재위험

2-sec-Butylphenol is combustible.

Safety Profile

A poison by intraperitoneal and intravenous routes. Moderately toxic by ingestion and skin contact. A severe skin and eye irritant. Combustible when exposed to heat or flame. To fight fire, use foam, spray, CO2, dry chemical. When heated to decomposition it emits acrid and irritating fumes. See also PHENOL and other butyl phenols

잠재적 노출

Butylphenols may be used as intermediates in manufacturing varnish and lacquer resins; as a germicidal agent in detergent disinfectants; as a pour point depressant, in motor-oil additives; de-emulsifier for oil; soap-antioxidant, plasticizer, fumigant, and insecticide

운송 방법

UN2430 Alkylphenols, solid, n.o.s. (including C2-C12 homologues), Hazard class: 8; Labels: 8— Corrosive material

비 호환성

Vapors may form explosive mixture with air. These phenol/cresol materials can react with oxidizers; reaction may be violent. Incompatible with strong reducing substances such as hydrides, nitrides, alkali metals, and sulfides. Flammable gas (H2) is often generated, and the heat of the reaction may cause the gas to ignite and explode. Heat is also generated by the acid-base reaction with bases; such heating may initiate polymerization of the organic compound. React with boranes, alkalies, aliphatic amines, amides, nitric acid, sulfuric acid. Phenols are sulfonated very readily (for example, by concentrated sulfuric acid at room temperature). These reactions generate heat. Phenols are also nitrated very rapidly, even by dilute nitric acid and can explode when heated. Many phenols form metal salts that may be detonated by mild shock

0-sec-부틸페놀 준비 용품 및 원자재

원자재

준비 용품


0-sec-부틸페놀 공급 업체

글로벌( 187)공급 업체
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Henan Tianfu Chemical Co.,Ltd.
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career henan chemical co
+86-0371-86658258
sales@coreychem.com China 29914 58
NINGBO INNO PHARMCHEM CO., LTD.
13867897135
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18871490254
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+8618530059196
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SIMAGCHEM CORP
+86-13806087780
sale@simagchem.com China 17367 58
Dayang Chem (Hangzhou) Co.,Ltd.
571-88938639 +8617705817739
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+86-89586680 +86-13289823923
1026@dideu.com China 9165 58
LEAP CHEM CO., LTD.
+86-852-30606658
market18@leapchem.com China 24738 58

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