디에틸에테르
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디에틸에테르 속성
- 녹는점
- -116 °C
- 끓는 점
- 34.6 °C(lit.)
- 밀도
- 0.714
- 증기 밀도
- 2.6 (vs air)
- 증기압
- 28.69 psi ( 55 °C)
- 굴절률
- n
20/D 1.3530(lit.)
- 인화점
- -40 °F
- 저장 조건
- Store at RT.
- 용해도
- 물에 용해되며 에탄올(96%), 염화메틸렌 및 지방유와 혼합됩니다. 가연성이 높습니다.
- 물리적 상태
- 액체
- Specific Gravity
- 0.714 (20/4℃) ; 0.712 (25℃)
- 색상
- clearAPHA: ≤10
- 냄새
- 0.33ppm에서 매운 냄새 감지 가능
- 상대극성
- 2.9
- 폭발한계
- 1.7-36%(V)
- 수용성
- 69g/L(20℃)
- 어는점
- -116.3℃
- Merck
- 14,3806
- Henry's Law Constant
- 12.50(x 10-4 atm?m3/mol at 25 °C) (Signer et al., 1969)
- 노출 한도
- TLV-TWA 1200 mg/m3 (400 ppm) (ACGIH and OSHA); STEL 1500 mg/m3 (500 ppm) (ACGIH).
- Dielectric constant
- 4.0(40℃)
- 안정성
- Stable, but light-sensitive, sensitive to air. May contain BHT (2,6-di-tert-butyl-4-methylphenol) as a stabilizer. Substances to be avoided include zinc, halogens, halogen-halogen compounds, nonmetals, nonmetallic oxyhalides, strong oxidizing agents, chromyl chloride, turpentine oils, turps substitutes, nitrates, metallic chlorides. Extre
- LogP
- 0.890
- 표면장력
- 17.153mN/m at 293.15K
- CAS 데이터베이스
- 60-29-7(CAS DataBase Reference)
안전
- 위험 및 안전 성명
- 위험 및 사전주의 사항 (GHS)
위험품 표기 | F+,Xn,T,F | ||
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위험 카페고리 넘버 | 12-19-22-66-67-39/23/24/25-23/24/25-11 | ||
안전지침서 | 9-16-29-33-45-36/37-7 | ||
유엔번호(UN No.) | UN 1155 3/PG 1 | ||
WGK 독일 | 1 | ||
RTECS 번호 | KI5775000 | ||
F 고인화성물질 | 10 | ||
자연 발화 온도 | 160 °C | ||
TSCA | Yes | ||
HS 번호 | 2909 11 00 | ||
위험 등급 | 3 | ||
포장분류 | I | ||
유해 물질 데이터 | 60-29-7(Hazardous Substances Data) | ||
독성 | LD50 oral (rat) 1215 mg/kg LC50 inhal (rat) 73,000 ppm (2 h) PEL (OSHA) 400 ppm STEL (ACGIH) 500 ppm |
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IDLA | 1,900 ppm [10% LEL] | ||
기존화학 물질 | KE-27690 |
디에틸에테르 C화학적 특성, 용도, 생산
물성
무색의 유동하지 않는 액체인데 단맛, 자극적인 냄새가 있다. 녹는점 -116.2℃, 끓는점 34.5℃, 0.7135, 1.35424. 알코올과 임의의 비율로 혼합되고 물에 조금 녹는다. 휘발성으로 인화되기 쉽고 공기와의 혼합물은 폭발을 일으킨다. 공기에 의해 복잡한 산화를 받아 과산화물을 만든다. 할로겐, 클로로포름, 금속염 등과 첨가 화합물을 형성한다. 6국에는 에테르 및 마취용 에테르가 기록되어 있다. 모두 에틸에테르 함량 96~98%, 소량의 에틸알코올 및 물을 함유한다.용도
1) 마취용 에테르는 물로 씻어 염화칼슘으로 건조하고 재증류하여 만든다. 약국방에서는 특히 용기에서 꺼내 24시간 이상 경과한 것을 마취용으로 사용하면 안 되는 것을 주의로 규정하고 있다. 이것은 광선과 공기 중의 산소에 의해 자동 산화를 일으켜 아세트알데히드와 과산화물을 생성하고 특히 후자는 폐렴, 기관지염을 일으키기 쉽기 때문이다. 흡입 마취약으로 가장 많이 사용된다. 2) 금속의 염화물을 염산 용액에서 추출 분리하는 데 사용되는 중요한 시약의 하나.합성
알코올에 진한 황산을 첨가하고 가열하여 유출시킨다. 공업적으로는 에틸렌에서 에틸알코올 합성시의 부산물로 얻어진다.개요
Diethyl ether is a component of starting fluids and is used as a solvent in the manufacture of synthetic dyes and plastics. Because of its characteristics, diethyl ether was widely used in many countries as an anesthetic agent, but was then replaced by other substances in the 1960s.화학적 성질
Ether, (C2H5)2,also known as ethyl ether, is a colorless liquid. It is used as a solvent,a denaturant, and as an anesthetic in medicine. lt is an organic compound in which two hydrocarbon radicals are joined by an atom of oxygen.물리적 성질
Colorless, hygroscopic, volatile liquid with a sweet, pungent odor. Odor threshold concentration is 330 ppb (quoted, Keith and Walters, 1992).역사
Ether was supposedly discovered by Raymundus Lullus (1232–1315) around 1275, although there is no extant evidence of this in his writings. The discoverer of ether is often credited to the German physician and botanist Valerius Cordus (1515–1554), who gave the first description of the preparation of ether in the mid-16th century. Cordus called the substance oleum vitrioli dulce, which is translated as sweet oil of vitriol. Cordus used sulfuric acid (oil of vitriol) to catalyze the conversion of alcohol to ether. At approximately the same time Paracelsus (1493–1541), a Swiss physician who is also cited as a discoverer of ether, observed that chickens were safely put to sleep by breathing vapors from sweet oil of vitriol. In 1730, August Siegmund Frobenius changed the name of sweet vitriol to ether.용도
Diethyl ether has been used extensively as a general anesthetic.생산 방법
Ether is produced by the dehydration of ethanol using sulfuric acid: 2CH3CH2OH +2H2SO4 → (CH3CH2)2O + H2SO4 + H2O.the temperature of the reaction is carriedout at about 140°C to control for unwanted products.the volatile ether is distilled from themixture. Ether can also be prepared by Williamson synthesis. In this reaction, ethanol reactswith sodium to form sodium ethanolate (Na+C2H5O?). Sodium ethanolate then reacts withchloroethane to form ether and sodium chloride: Na+C2H5O? +C2H5Cl → C2H5OC2H5 +NaCl. Ether is also produced as a by-product in the production of ethanol.정의
diethyl ether: A colourless flammablevolatile ether, C2H5OC2H5; r.d. 0.71;m.p. –116°C; b.p. 34.5°C. It can bemade by Williamson’s synthesis. Itis an anaesthetic and useful organicsolvent.일반 설명
A clear colorless liquid with an anesthetic odor. Flash point -49°F. Less dense than water and slightly soluble in water. Hence floats on water. Vapors are heavier than air. Used as a solvent and to make other chemicals.공기와 물의 반응
Highly flammable. Oxidizes readily in air to form unstable peroxides that may explode spontaneously [Bretherick, 1979 p.151-154, 164]. A mixture of liquid air and Diethyl ether exploded spontaneously, [MCA Case History 616(1960)].반응 프로필
Occasional explosions have occurred when aluminum hydride was stored in ether. The explosions have been blamed on the presence of carbon dioxide impurity in the ether, [J. Amer. Chem. Soc. 70:877(1948)]. Diethyl ether and chromium trioxide react violently at room temperature. Solid acetyl peroxide in contact with ether or any volatile solvent may explode violently. A 5-gram portion in ether detonated while being carried, [Chem. Eng. News 27:175(1949)]. Nitrosyl perchlorate ignites and explodes with Diethyl ether. A mixture of ether and ozone forms aldehyde and acetic acid and a heavy liquid, ethyl peroxide, an explosive, [Mellor 1:911(1946-1947)].위험도
CNS depressant by inhalation and skin absorption. Very flammable, severe fire and explosion hazard when exposed to heat or flame. Forms explosive peroxides. Explosive limits in air 1.85– 48%.건강위험
The acute toxicity of diethyl ether is low. Inhalation of high concentrations can cause sedation, unconsciousness, and respiratory paralysis. These effects are usually reversible upon cessation of exposure. Diethyl ether is mildly irritating to the eyes and skin, but does not generally cause irreversible damage. Repeated contact can cause dryness and cracking of the skin due to removal of skin oils. The liquid is not readily absorbed through the skin, in part because of its high volatility. Diethyl ether is slightly toxic by ingestion. Diethyl ether is regarded as having adequate warning properties. There is no evidence for carcinogenicity of diethyl ether, and no reproductive effects have been reported. Chronic exposure to diethyl ether vapor may lead to loss of appetite, exhaustion, drowsiness, dizziness, and other central nervous system effects.화재위험
Diethyl ether is extremely flammable (NFPA rating = 4) and is one of the most dangerous fire hazards commonly encountered in the laboratory, owing to its volatility and extremely low ignition temperature. Ether vapor may be ignited by hot surfaces such as hot plates and static electricity discharges, and since the vapor is heavier than air, it may travel a considerable distance to an ignition source and flash back. Ether vapor forms explosive mixtures with air at concentrations of 1.9 to 36% (by volume). Carbon dioxide or dry chemical extinguishers should be used for ether fires. Diethyl ether forms unstable peroxides on exposure to air in a reaction that is promoted by light; the presence of these peroxides may lead to explosive residues upon distillation.인화성 및 폭발성
Diethyl ether is extremely flammable (NFPA rating = 4) and is one of the most dangerous fire hazards commonly encountered in the laboratory, owing to its volatility and extremely low ignition temperature. Ether vapor may be ignited by hot surfaces such as hot plates and static electricity discharges, and since the vapor is heavier than air, it may travel a considerable distance to an ignition source and flash back. Ether vapor forms explosive mixtures with air at concentrations of 1.9 to 36% (by volume). Carbon dioxide or dry chemical extinguishers should be used for ether fires. Diethyl ether forms unstable peroxides on exposure to air in a reaction that is promoted by light; the presence of these peroxides may lead to explosive residues upon distillation.화학 반응
Reactivity with Water No reaction; Reactivity with Common Materials: No reaction; Stability During Transport: Stable; Neutralizing Agents for Acids and Caustics: Not pertinent; Polymerization: Not pertinent; Inhibitor of Polymerization: Not pertinent.공업 용도
Diethyl ether as a commercial product is available in several grades and is used as an extraction solvent, reaction solvent, and as a general anesthetic. Ethyl ether is an excellent solvent for alkaloids, dyes, fats, gums, oils, resins, and waxes. Blends of ethyl ether and ethanol are excellent solvents for cellulose nitrate used in the manufacture of guncotton, in collodion solutions and pyroxylin plastics. Ethyl ether is used in the recovery of acetic acid from aqueous solutions in the cellulose acetate and plastic industry. It is used as a starter fuel for diesel engines and as a denaturant in denatured ethanol formulations. Grignard and Wurtz-Fillig synthesis reactions use diethyl ether as an anhydrous, inert reaction medium.잠재적 노출
Ethyl ether is used as a solvent for waxes, fats, oils, perfumes, alkaloids, dyes, gums, resins, nitrocellulose, hydrocarbons, raw rubber, and smokeless powder. It is also used as an inhalation anesthetic; a refrigerant; in diesel fuels; in dry cleaning; as an extractant; and as a chemical reagent for various organic reactions환경귀착
Photolytic. The rate constant for the reaction of ethyl ether and OH radicals in the atmosphere at 300 K is 5.4 x 10-12 cm3/molecule?sec (Hendry and Kenley, 1979).Chemical/Physical. The atmospheric oxidation of ethyl ether by OH radicals in the presence of nitric oxide yielded ethyl formate as the major product. Minor products included formaldehyde and nitrogen dioxide. In the absence of nitric oxide, the products were ethyl formate and acetaldehyde (Wallington and Japar, 1991).
Ethyl ether will not hydrolyze (Kollig, 1993).
저장
ether should be used only in areas free of ignition sources (including hot plates, incandescent light bulbs, and steam baths), and this substance should be stored in tightly sealed metal containers in areas separate from oxidizers. Because of the tendency of diethyl ether to form peroxides on contact with air, containers should be dated upon receipt and at the time they are opened. Diethyl ether is generally supplied with additives that inhibit peroxide formation; distillation removes these inhibitors and renders the liquid more prone to peroxide formation. Material found to contain peroxides should be treated to destroy the peroxides before use or disposed of properly.운송 방법
UN1155 Diethyl ether or Ethyl ether, Hazard Class: 3; Labels: 3-Flammable liquid비 호환성
May form explosive mixture with air. Incompatible with strong acids; strong oxidizers halogens, sulfur, sulfur compounds, causing fire and explosion hazard. Can form peroxides from air, heat, sunlight; may explode when container is unstoppered or otherwise opened. Attacks some plastics, rubber and coatings. Being a nonconductor, chemical may accumulate static electric charges that may result in ignition of vapor.폐기물 처리
Concentrated waste containing no peroxides-discharge liquid at a controlled rate near a pilot flame. Concentrated waste containing peroxidesperforation of a container of the waste from a safe distance followed by open burning. Consult with environmental regulatory agencies for guidance on acceptable disposal practices. Generators of waste containing this contaminant (≥100 kg/mo) must conform with EPA regulations governing storage, transportation, treatment, and waste disposal디에틸에테르 준비 용품 및 원자재
원자재
준비 용품
2-페닐-2-프로판올
피리딘보란 부가물
6-MORPHOLINONICOTINALDEHYDE
2-Methoxy-5-pyridineboronic acid
2-Methoxyphenylboronic acid
(6-ETHOXYPYRIDIN-3-YL)BORONIC ACID
1,2-(Methylenedioxy)-4-nitrobenzene
락타마이드
2-Bromo-4-nitro-1-(trifluoromethoxy)benzene
N,N,N',N'-TETRAMETHYL-2-BUTENE-1,4-DIAMINE
2-(4-Ethoxyphenyl)-2-methylpropanol
2-[5-(Benzyloxy)-1H-indol-3-yl]-2-oxoacetic acid ,97%
포스포몰리브드 산 수화물
2-Bromo-1-indanone
1,5-헥사다이엔
4-tert-Butylbenzoyl chloride
2,6-Difluorophenylboronic acid
에틸1-메틸피롤-2-카르복실레이트
멜라노사이트초콜릿호르몬합성
3-메틸벤질아민
티아나프텐-2-붕소산
엑고닌염화물아미노알코올부분
제니스테인
17beta-Hydroxy-17-methylandrosta-4,9(11)-dien-3-one
2-아세틸티아졸
7-OXABICYCLO[2.2.1]HEPTANE
에틸렌디아민디아세테이트
카보닐산알릴메틸에스테르
N-Boc-N,N-비스(2-클로로에틸)아민
N,N-디에틸-1-프로피닐아민
레보노게스트렐
다이드제인
2,4-Dibromothiophene
2-Amino-6-methyl-4-pyrimidinol
2,2′:5′,2′′-터티오펜
4-(Trifluoromethyl)phenacyl bromide
1-메틸-1H-피라졸-5-카르복실산
에폭시옥탄(1,2-)
methylated albumin
3-(4-브로모페녹시)프로판산