클로로포름
클로로포름 · R20(냉각제) · 메탄트리염화물(METHANETRICHLORIDE)메틸트리염화물 · 메테닐트리염화물 · 클로로폼 · 트리클로로메탄 · 트리클로로메탄,클로로포롬 · 트리클로로포름

식별자 및 물리적 특성
| CAS No. | 67-66-3 |
|---|---|
| 분자식 | CHCl3 |
| 평균 분자량 | 119.37 g/mol |
| 단동위원소 질량 | 117.914383 g/mol |
| SMILES | ClC(Cl)Cl |
| InChIKey | HEDRZPFGACZZDS-UHFFFAOYSA-N |
| PubChem CID | 6212 |
| ChEMBL | CHEMBL44618 |
| ChEBI | CHEBI:35255 |
| EC No. | 200-663-8 |
| DTXSID | DTXSID1020306 |
| 현지명 | 클로로포름 |
화학 및 물리적 성질
| XLogP | 2.3 |
|---|---|
| 극성 표면적 | 0 |
| 수소 결합 공여자 수 | 0 |
| 수소 결합 수용자 수 | 0 |
| 회전 가능 결합 수 | 0 |
| 무거운 원자 수 | 4 |
| 형식 전하 | 0 |
| 복잡도 | 8 |
| 물질 분류 | Hazardous Air Pollutants (HAPs)Urban Hazardous Air Pollutants (HAPs) - EPA specified greatest potential health threat in urban areasCarcinogens |
| Solvents | Solvents -> Chlorinated Aliphatics |
| SpringerMaterials Properties | Coriolis coupling |
| 농약 | Pesticide -> EPA IRISVolatile Organic Compound (VOC) (Pesticide/Volatile Organic Compound (VOC)) |
| LogP(분배 계수) | log Kow = 1.97 |
| 냄새 | Pleasant, etheric, nonirritatingPleasant odorOdor threshold: 205-307 ppmCharacteristic odor133~276ppm(평균 = 192ppm)에서 감지 가능한 미묘하고 달콤한 냄새 |
| 맛 | Sweet taste |
| 식품 첨가물 | PROCESSING AID -> FDA Substance added to food |
| 밀도 | 1.4832 at 68 °F (EPA, 1998) - Denser than waterwill sink1.4788 g/cu cm at 25 °CDensity: 1.484 at 20 °C/20 °CAn alcholic solution of chloroform containing 6% by volume of chloroform, corresponding to 10.5% by weight and approximately 89% absolute alcohol by volume. Colorless, clear liquid. Chloroform odor. Density: approximately 0.85 /Spirit of chloroform/Density (at 20 °C): 1.48 g/mlRelative density of the vapour/air-mixture at 20 °C (air = 1): 1.71.492 g/mL at 25 °C(lit.) |
| Viscosity | 5.63 millipoises at 20 °C5.10 millipoises at 30 °C |
| Color/Form | Highly refractive, nonflammable, heavy, very volatile liquidClear, colorless liquidColorless, highly refractive, heavy volatile liquid. |
| 용해도 | less than 1 mg/mL at 66 °F (NTP, 1992)In water, 7.95X10+3 mg/L at 25 °CHighly soluble in waterOne mL dissolves in about 200 mL water at 25 °CMiscible with alcohol, benzene, ether, petroleum ether, carbon tetrachloride, carbon disulfide, oilsFor more Solubility (Complete) data for Chloroform (6 total), please visit the HSDB record page.디에틸 에테르, 오일, 리그로인, 알코올, 사염화탄소 및 이황화탄소와 혼합 가능합니다. |
| 녹는점 | -63 °C |
| 끓는 점 | 61 °C |
| 증기 밀도 | 4.1 (vs air) |
| 증기압 | 160 mm Hg ( 20 °C) |
| 굴절률 | n20/D 1.445(lit.) |
| 인화점 | 60.5-61.5°C |
| 저장 조건 | 2-8°C |
| pKa(산도 계수) | 15,5(at 25℃) |
| 물리적 상태 | 액체 |
| 색상 | ≤10(APHA) |
| 후각 역치 | 3.8ppm |
| 용해도 | 8g/L(20℃) |
| 비열 | Cp(liquid): 0.96 J/(g·K)Cp(gas): 0.55 J/(g·K), at 25℃ |
| Merck | 14,2141 |
| BRN | 1731042 |
| 헨리 상수 | 1.07 at 2 °C, 1.49 at 6 °C, 1.79 at 10 °C, 3.02 at 18 °C, 4.02 at 25 °C, 5.20 at 30 °C, 7.60 at 40 °C, 11.1 at 50 °C, 14.8 at 60 °C (EPICS-SPME-GC, Grgényi et al., 2002)) |
| 유전율 | 5.5(0℃) |
| 안정성 | 휘발성 물질 |
| 화장품 원료 기능 | 용제 |
| InChI | 1S/CHCl3/c2-1(3)4/h1H |
| InChIKey | HEDRZPFGACZZDS-UHFFFAOYSA-N |
| SMILES | ClC(Cl)Cl |
| LogP(분배 계수) | 1.970 |
| 표면장력 | 27.5mN/m at 20°C |
| NIST | Chloroform(67-66-3) |
| EPA | Chloroform (67-66-3) |
화학적 성질
Chloroform is a noncombustible, clear, colorless liquid with a pleasant, sweet odor. The Odor Threshold is 12 ppm.
안전 및 규제
| GHS 분류 | DangerH302: Harmful if swallowed [Warning Acute toxicity, oral]P203, P260, P261, P264, P264+P265, P270, P271, P280, P301+P317, P302+P352, P304+P340, P305+P351+P338, P316, P318, P319, P321, P330, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)This chemical does not meet GHS hazard criteria for < 0.1% (1 of 1499) of reports.H302 (94.8%): Harmful if swallowed [Warning Acute toxicity, oral] |
|---|---|
| 규제 정보 | Chemical: Methane, trichloro-Hazard Traits - CarcinogenicityCardiovascular ToxicityDevelopmental ToxicityHepatotoxicity and Digestive System ToxicityNephrotoxicity and Other Toxicity to the Urinary SystemNeurotoxicityReproductive ToxicityRespiratory ToxicityMethane, trichloro- is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of Methane, trichloro- are required to report information about their production and use of this chemical to the EPA under the Toxic Substances Control Act (TSCA). (40 eCFR Part 711)REACH registered substance: Chloroform (EC: 200-663-8)Restricted substance: ChloroformChloroform: HSNO Approval: HSR002937 Approved with controls |
| 기타 안전 정보 | IMAP assessments - Methane, trichloro-: Human health tier II assessment |
| 운송 라벨(DOT) | Poison |
| 화재 위험 | Container may explode in the heat of fire. When heated it liberates phosgene, hydrogen chloride, chlorine and toxic and corrosive oxides of carbon and chlorine. Chloroform explodes when in contact with aluminum powder or magnesium powder or with alkali metals (e.g., lithium, sodium, and potassium) and dinitrogen tetroxide. It reacts vigorously with acetone in the presence of potassium hydroxide or calcium hydroxide. It is oxidized by strong oxidizers such as chromic acid forming phosgene and chlorine. It reacts vigorously with triisopropylphosphine. It develops acidity from prolonged exposure to air and light. (EPA, 1998)· Non-combustible, substance itself does not burn but may decompose upon heating to produce corrosive and/or toxic fumes.Not combustible. Gives off irritating or toxic fumes (or gases) in a fire. Risk of fire and explosion on contact with incompatible substances. See Chemical Dangers. |
용도
용도
클로로포름이 사람에게 처음 마취제로서 투약되었고,마취 효과가 빠르고 강하게 나타나 수술용 마취제로 널리 사용되게 되었습니다.하지만 시간이 지나면서 마취용 클로로포름 사용에 의해 환자가 사망하는 사건들이 발생하고, 더욱 안전한 마취제들이 새롭게 등장하며 더 이상 마취제로 사용되지 않게 되었습니다. 클로로포름은 현재 주로 살충제와 곰팡이 제거제로 많이 사용되며,지방과 오일, 고무, 알칼로이드, 왁스 등의 용매제 및 분석 시약으로도 사용되고 있습니다.
개요
Chloroform is a trichlorinated organic substance with the chemical formula of CHCl3. It is a clear liquid at room temperature and has a pleasant, sweet odor. Chloroform is only slightly soluble in water and evaporates quickly into surrounding air, increasing the risk of inhalation exposure. In addition, chloroform persists for a long time in both water and air. There are no natural sources of chloroform, but this contaminant enters the environment through a variety of industrial operations, including the chlorination of water. Humans can be exposed to chloroform through inhalation, ingestion, and dermal contact. Chloroform has a relatively narrow margin of safety and has been replaced by better inhalation anesthetics. In addition, it is believed to be toxic to the liver and kidneys and may cause liver cancer. Chloroform was once widely used as a solvent, but safety and environmental concerns have reduced this use as well. Nevertheless, chloroform has remained an important industrial chemical.
역사
Chloroform (CHCl3) was first discovered in 1831 by American physician Samuel Guthrie; and independently a few months later by Frenchman Eugène Soubeiran and Justus von Liebig in Germany. Chloroform was named and chemically characterised in 1834 by Jean-Baptiste Dumas. Its anaesthetic properties were noted early in 1847 by Marie-Jean-Pierre Flourens. Unlike ether, chloroform's characteristically sweet odour isn't irritating, although inhalation of concentrated chloroform vapour may cause irritation of exposed mucous surfaces. Chloroform is a more effective anaesthetic than nitrous oxide. In 1864, the Report of Chloroform Committee of Royal Medical and Chirurgical Society endorsed chloroform as Britain's favourite anaesthetic. But ether was safer for patients. In 1871, leading anaesthetic manufacturer Edward E. Squibb of Brooklyn estimated [New York Medical Journal (April 1871) 13;389] that of 400,000 administrations of anaesthesia in the USA in 1870, chloroform was the agent used in some 50%, ether for 40%, and other gases and mixtures accounted for the rest.
용도
Chloroform is a widely used industrial and laboratory solvent. It is a volatile chlorinated organic solvent whose vapors have a narcotic effect.Due to its light sensitivity, it may undergo degradation with time. This can be suppressed by adding ethanol as a stabilizer. The addition will increase the polarity of the solvent and potentially impact certain applications. Chloroform has been used as a solvent for dissolving lipids and also as a cleansing agent. It may also be used in solvent extraction process and also for recrystallization. Suitable for HPLC, spectrophotometry, environmental testing Facilitates recovery of the aqueous phase of PCRs which have been overlaid with mineral oil. Meets ACS specifications.
제조 및 합성 방법
생산 방법
Chloroform was first synthesized by treating acetone or ethanol with calcium hypochlorite or sodium hypochlorite bleaching powder. Chlorination of ethanol produces acetaldehyde and then trichloroacetaldehyde. Acetaldehyde yields chloroform and the formate ion by action of hydroxide ion. Acetone is chlorinated to trichloroacetone, which then splits into chloroform and the acetateion. The modern industrial preparation of chloroform involves the chlorination of methane or methyl chloride, CH3Cl, using heat to substitute the chlorine atoms for hydrogen. The reaction is carried out at approximately 500°C. Hydrochlorination by reacting methanol and hydrogen chloride can also be used to produce chloroform.