P-크레졸

P-크레졸
P-크레졸 구조식 이미지
카스 번호:
106-44-5
한글명:
P-크레졸
동의어(한글):
P-크레솔;p-크레졸;크레졸;1-메틸-4-하이드록시벤젠;1-하이드록시-4-메틸벤젠;4-메틸페놀;4-크레솔;4-크레졸;4-하이드록시-1-메틸벤젠;4-하이드록시톨루엔;P-하이드록시톨루엔;크레솔, P-;파라-크레실릭산
상품명:
p-Cresol
동의어(영문):
4-METHYLPHENOL;para-cresol;P-HYDROXYTOLUENE;4-Cresol;P-METHYLPHENOL;p-Tolyl alcohol;Paracresol;Phenol,4-methyl-;Paramethyl phenol;p-Cresol, extra pure
CBNumber:
CB5453502
분자식:
C7H8O
포뮬러 무게:
108.14
MOL 파일:
106-44-5.mol
MSDS 파일:
SDS

P-크레졸 속성

녹는점
32-34 °C(lit.)
끓는 점
202 °C(lit.)
밀도
1.034 g/mL at 25 °C(lit.)
증기 밀도
3.72 (vs air)
증기압
1 mm Hg ( 20 °C)
FEMA
2337 | P-CRESOL
굴절률
nD20 1.5395
인화점
193 °F
저장 조건
Store below +30°C.
용해도
20g/L
산도 계수 (pKa)
10.17(at 25℃)
물리적 상태
결정질 고체 또는 액체
색상
무색~연황색, 빛에 노출되면 어두워질 수 있음
Specific Gravity
1.0341 (20/4℃)
냄새
디프로필렌 글리콜 중 0.10%. 페놀 수선화 동물 미모사
?? ??
페놀성
Odor Threshold
0.000054ppm
폭발한계
1%(V)
수용성
20g/L(20℃)
감도
Light Sensitive
JECFA Number
693
Merck
14,2579
BRN
1305151
Henry's Law Constant
6.17 at 20.00 °C, 9.31 at 25.00 °C (dynamic equilibrium system-GC, Feigenbrugel et al., 2004a)
노출 한도
NIOSH REL: TWA 2.3 ppm (10 mg/m3), IDLH 250 ppm; OSHA PEL: TWA 5 ppm (22 mg/m3); ACGIH TLV: TWA for all isomers 5 ppm (adopted).
Dielectric constant
5.6(21.0℃)
안정성
안정적인. 타기 쉬운. 강한 산화제와 호환되지 않습니다. 공기와 빛에 민감합니다. 흡습성.
LogP
1.94
CAS 데이터베이스
106-44-5(CAS DataBase Reference)
NIST
Phenol, 4-methyl-(106-44-5)
EPA
p-Cresol (106-44-5)
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
위험품 표기 T,Xi
위험 카페고리 넘버 24/25-34-39/23/24/25-23/24/25
안전지침서 36/37/39-45-36/37
유엔번호(UN No.) UN 3455 6.1/PG 2
WGK 독일 1
RTECS 번호 GO6475000
F 고인화성물질 8
자연 발화 온도 555 °C
위험 참고 사항 Irritant
TSCA Yes
위험 등급 6.1
포장분류 II
HS 번호 29071200
유해 물질 데이터 106-44-5(Hazardous Substances Data)
독성 LD50 orally in rats: 1.8 g/kg (Deichmann, Witherup)
기존화학 물질 KE-24794
유해화학물질 필터링 97-1-268
함량 및 규제정보 물질구분: 유독물질; 혼합물(제품)함량정보: 크레졸 및 이를 5% 이상 함유한 혼합물
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
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:
P260 분진·흄·가스·미스트·증기·...·스프레이를 흡입하지 마시오.
P270 이 제품을 사용할 때에는 먹거나, 마시거나 흡연하지 마시오.
P280 보호장갑/보호의/보안경/안면보호구를 착용하시오.
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
2
3 0

P-크레졸 MSDS


4-Methylphenol

P-크레졸 C화학적 특성, 용도, 생산

물성

무색 황색을 띠는 투명한 액체.

용도

P- 크레졸,흰색 또는 무색 결정. 알코올에 용해, 에테르, 클로로포름 및 온수에. 주요 용도: 의학, 살충제, 향수, 합성 수지 및 염료, 등.

화학적 성질

Cresol is a mixture of three isomeric forms: o-, m-, and p-cresol. These compounds are slightly soluble in water. The m-isomer is a colorless or yellow liquid with characteristic odor. The p-cresol is a colorless to pink crystals with a characteristics phenol-like odor. The concentration at which the odor becomes detectable in water is 55 parts per billion (Buttery et al., 1988). Another study by Leonardos et al. (1969) reported an experimental odor threshold concentration of 1 parts per billion, which is higher than the 0.054 parts per billion reported by Nagata and Takeuchi (1990).

출처

Has been found in a score of essential oils including ylang ylang and oil of jasmine (Gildemeister & Hoffman, 1966).

용도

p-Cresol is utilized in the production of artificial resins, liquid crystal intermediates, disinfectants, fumigants, and as an industrial solvent. It is also involved in the manufacturing of Bupranolol, a non-selective beta blocker.

정의

ChEBI: P-cresol is a cresol that consists of toluene substituted by a hydroxy group at position 4. It is a metabolite of aromatic amino acid metabolism produced by intestinal microflora in humans and animals. It has a role as a uremic toxin, a human metabolite and an Escherichia coli metabolite.

생산 방법

The cresols (cresylic acids) are methyl phenols and generally appear as a mixture of isomers. p-Cresol is a 4-methyl derivative of phenol and is prepared from m-toluic acid or obtained from coal tar or petroleum. Crude cresol is obtained by distilling “gray phenic acid” at a temperature of ~180–201°C. p-Cresol may be separated from the crude or purified mixture by repeated fractional distillation in vacuo. It can also be prepared synthetically by diazotization of the specific toluene or by fusion of the corresponding toluenesulfonic acid with sodium hydroxide.

제조 방법

It can be prepared by fractional distillation of coal tar where it occurs together with the ortho- and para- isomers.

일반 설명

Colorless solid with a tar like odor. Sinks and mixes slowly with water.

공기와 물의 반응

Insoluble in water.

반응 프로필

p-Cresol is sensitive to heat. p-Cresol is also sensitive to light. p-Cresol is incompatible with strong oxidizers and strong alkalis. p-Cresol will attack some forms of plastics, coatings and rubber.

건강위험

INHALATION: Irritation of nose or throat. EYES: Intense irritation and pain, swelling of conjunctiva and corneal damage may occur. SKIN: Intense burning, loss of feeling, white discoloration and softening. Gangrene may occur. INGESTION: Burning sensation in mouth and esophagus. Vomiting may result. Absorption by all routes may cause muscular weakness, gastroenteric disturbance, severe depression and collapse. Effects are primarily on central nervous system, edema of lungs, injury of spleen and pancreas may occur.

Safety Profile

Poison by ingestion, skin contact, subcutaneous, intravenous, and intraperitoneal routes. A severe skin and eye irritant. Questionable carcinogen with experimental neoplastigenic data by itself and with 7,12-dirnethyl benz(a)anthracene. Combustible when exposed to heat or flame. Moderately explosive in the form ofvapor when exposed to heat or flame. To fight fire, use CO2, dry chemical, alcohol foam. See also other cresol entries and PHENOL.

잠재적 노출

Cresol is used as a disinfectant and fumigant; as an ore flotation agent, and as an intermediate in the manufacture of chemicals, dyes, plastics, and antioxidants. A mixture of isomers is generally used; the concentrations of the components are determined by the source of the cresol.

Carcinogenicity

o-Cresol has been induced a few papillomas but no carcinomas in tumor studies.

신진 대사

p-Cresol is oxidized at the methyl group in both dogs and rabbits to yield ρ-hydroxybenzoic acid. In the rabbit up to 10% of oral doses of 0.25-0.5 g is excreted as free and conjugated p-hydroxybenzoic acid (Williams, 1959).

운송 방법

UN2076 Cresols, liquid, Hazard class: 6.1; Labels: 6.1-Poisonous materials, 8-Corrosive material. UN3455 Cresols, solid, Hazard class: 6.1; Labels: 6.1- Poisonous materials, 8-Corrosive material.

Purification Methods

It can be separated from m-cresol by fractional crystalisation of its melt. Purify it by distillation, by precipitation from *benzene solution with pet ether, and via its benzoate, as for phenol. Dry it under vacuum over P2O5. It has also been crystallised from pet ether (b 40-60o) and by conversion to sodium p-cresoxyacetate which, after crystallisation from water is decomposed by heating with HCl in an autoclave [Savard Ann Chim (Paris) 11 287 1929]. The 3,5-dinitrobenzoate (prepared with 3,5-dinitrobenzoyl chloride in dry pyridine, and recrystallised from EtOH or aqueous Me2CO) has m 189o. [Beilstein 6 II 2093.]

비 호환성

Vapors may form explosive mixture with air. Incompatible with strong acids; oxidizers, alkalies, aliphatic amines; amides, chlorosulfonic acid; oleum. Decomposes on heating, producing strong acids and bases, causing fire and explosion hazard. Liquid attacks some plastics and rubber. Attacks many metals.

폐기물 처리

Wastewaters may be subjected to biological treatment. Concentrations may be further reduced by ozone treatment. High concentration wastes may be destroyed in special waste incinerators.

P-크레졸 준비 용품 및 원자재

원자재

준비 용품


P-크레졸 공급 업체

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