크로톤알데하이드
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크로톤알데하이드 속성
- 녹는점
- −76 °C(lit.)
- 끓는 점
- 104 °C(lit.)
- 밀도
- 0.853 g/mL at 20 °C(lit.)
- 증기 밀도
- 2.41 (vs air)
- 증기압
- 32 mm Hg ( 20 °C)
- 굴절률
- n
20/D 1.437
- 인화점
- 48 °F
- 저장 조건
- 2-8°C
- 용해도
- 알코올, 벤젠, 휘발유, 등유, 솔벤트 나프타, 톨루엔과 혼합 가능(Hawley, 1981)
- 물리적 상태
- 무색의 액체
- 색상
- 무색
- Odor Threshold
- 0.023ppm
- 수용성
- 물에 용해됩니다. (150g/L), 20°C에서.
- 감도
- Air Sensitive
- Merck
- 13,2624
- BRN
- 1209254
- Henry's Law Constant
- 1.92 x 10-5 atm?m3/mol (Buttery et al., 1971)
- 노출 한도
- NIOSH REL: TWA 2 ppm (6 mg/m3), IDLH 50 ppm; OSHA PEL: TWA 2 ppm; ACGIH TLV: ceiling 0.3 ppm (adopted).
- 안정성
- Air sensitive. Highly flammable. Readily forms explosive mixtures with air. May polymerize in the presence of acids, alkalies or amines. Uncontrolled polymerisation may lead to a rapid temperature rise. Incompatible with acids, bases, amines, strong oxidizing agents, butadiene, ketones, oxygen. May contain a stabilizer.
- LogP
- 0.6 at 25℃
- CAS 데이터베이스
- 4170-30-3(CAS DataBase Reference)
- IARC
- 3 (Vol. 63) 1995
안전
- 위험 및 안전 성명
- 위험 및 사전주의 사항 (GHS)
위험품 표기 | F,T+,N | ||
---|---|---|---|
위험 카페고리 넘버 | 11-24/25-26-37/38-41-48/22-50-68 | ||
안전지침서 | 26-28-36/37/39-45-61-16 | ||
OEB | B | ||
OEL | TWA: 2 ppm (6 mg/m3) (Aldehydes) | ||
유엔번호(UN No.) | UN 1143 6.1/PG 1 | ||
WGK 독일 | 3 | ||
RTECS 번호 | GP9625000 | ||
F 고인화성물질 | 9-13-23 | ||
TSCA | Yes | ||
위험 등급 | 6.1(a) | ||
포장분류 | I | ||
유해 물질 데이터 | 4170-30-3(Hazardous Substances Data) | ||
독성 | LD50 orally in rats: 0.3 g/kg (Smyth, Carpenter) | ||
IDLA | 50 ppm | ||
기존화학 물질 | KE-05-0370 | ||
유해화학물질 필터링 | 97-1-270 | ||
함량 및 규제정보 | 물질구분: 유독물질; 혼합물(제품)함량정보: 크로톤알데히드 및 이를 1% 이상 함유한 혼합물 |
크로톤알데하이드 C화학적 특성, 용도, 생산
화학적 성질
Crotonaldehyde is water-white (turns paleyellow on contact with air) with an irritating, pungent, suffocating odor.물리적 성질
Clear, colorless to straw-colored liquid with a pungent, irritating, suffocating odor. An odor threshold concentration of 23 ppbv was reported by Nagata and Takeuchi (1990). Katz and Talbert (1930) reported experimental detection odor threshold concentrations ranged from 180 to 570 μg/m3 (63 to 200 ppbv).용도
Crotonaldehyde is used in organic synthesis, in the manufacture of butyl alcohol and butyraldehyde, and as a warning agent in fuel gases. It is also used in the manufacture of nbutanol and sorbic acid as well as in the production of flavoring agents, surface-active agents, textiles, and insecticidal compounds.정의
Commercial crotonaldehyde is the trans isomer.일반 설명
A clear colorless to straw colored liquid with a penetrating pungent odor. Flash point 55°F. Density 7.1 lb / gal. Very toxic by inhalation. May polymerize with the release of heat under exposure to heat or contamination. If polymerization takes place inside a container, the container may rupture violently. Less dense than water. Vapors heavier than air.공기와 물의 반응
Highly flammable. Slightly soluble in water.반응 프로필
CROTONALDEHYDE can react violently with strong oxidizing reagents, e.g., reaction with conc. nitric acid leads to instantaneous ignition [Andrussow, L., Chim. Ind. (Paris), 1961, 86, p. 542]. In contact with strong acids or bases CROTONALDEHYDE will undergo an exothermic condensation reaction. Reaction with 1,3-butadiene is particularly violent [Greenlee, K. W., Chem. Eng. News, 1948, 26, p. 1985]. Crotonaldehyde may rapidly polymerize with ethyl acetoacetate (Soriano, D.S. et al. 1988. Journal of Chemical Education 65:637.).위험도
An animal carcinogen. Irritating to eyes, skin, and upper respiratory tract irritant. Flammable, dangerous fire risk. Explosive limits in air 2.9–15.5% by volume. Questionable carcinogen.건강위험
CROTONALDEHYDE is an extreme eye, respiratory, and skin irritant and can cause corneal damage. A 15 minute exposure at 4.1 ppm is highly irritating to the nose and upper respiratory tract and causes tearing. Brief exposure at 45 ppm proved very disagreeable with prominent eye irritation.화재위험
Flammable/combustible material; may be ignited by heat, sparks or flames. Vapor may travel to a source of ignition and flash back. Container may explode in heat of fire. Vapor explosion and poison hazard indoors, outdoors or in sewers. Runoff to sewer may create fire or explosion hazard. Readily converted by oxygen to hazardous peroxides and acids and is incompatible with caustics, ammonia, organic amines, mineral acids, and strong oxidizers. Readily resinifies to dimer when pure and slowly oxidizes to crotonic acid. Altered by light and air. Hazardous polymerization may occur. Polymerization may take place at high temperatures.Safety Profile
Suspected carcinogen with experimental carcinogenic data. Poison by ingestion and inhalation. Mutation data reported. An eye, skin, and mucous membrane irritant. A lachrymating material that can cause corneal burns and is very dangerous to the eyes. Caution: Keep away from heat and open flame. Keep container closed. Use with adequate ventilation. Extremely irritating to eyes, slim, mucous membranes. When necessary, the lachrymatory effect of the vapors may be counteracted by ammonia fumes. Dangerous fire hazard when exposed to heat or flame; can react with oxidizing materials. To fight fire, use alcohol foam, CO2, dry chemical. Reacts violently with 1,3 butadlene. Violent hypergolic reaction with concentrated nitric acid. When heated to decomposition it emits acrid smoke and fumes. See also ALDEHYDES.잠재적 노출
Crotonaldehyde is used as a warning agent in fuel gases and gas line leaks; as solvent; in Crotonaldehyde 935 chemical warfare; as an intermediate in the manufacture of n-butanol and crotonic and sorbic acids; in resin and rubber antioxidant manufacture; also used as a solvent in mineral oil purification; as an alcohol denaturant.Carcinogenicity
Similar to acrolein, crotonaldehyde is suspected of having tumorigenic activity and of involvement in the metabolism of N-nitrosopyrrolidine . Nevertheless, it has been proven that crotonaldehyde does have a carcinogenic effect on rats. Indeed, crotonaldehyde and nitrosopyrrolidine (a metabolite of crotonaldehyde) induced neoplastic lesions in the liver, hepatocellular carcinomas, neoplastic nodules, and liver damage when administered orally to rats over long periods of time.환경귀착
Biological. Heukelekian and Rand (1955) reported a 10-d BOD value of 1.30 g/g which is 56.8% of the ThOD value of 2.29 g/g.Chemical/Physical. Slowly oxidizes in air forming crotonic acid (Windholz et al., 1983). At elevated temperatures, crotonaldehyde may polymerize (NIOSH, 1997).
Crotonaldehyde undergoes addition of water across the CH=CH bond yielding 3- hydroxybutanal (Kollig, 1995).
At an influent concentration of 1,000 mg/L, treatment with GAC resulted in effluent concentration of 544 mg/L. The adsorbability of the carbon used was 92 mg/g carbon (Guisti et al., 1974).