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HCID 7932생성일: 2026년 10월 26일

M-클로로아닐린

1-프로펜-2-올,아세테이트 · m-아미노클로로벤젠 · M-클로로아닐린 · 1-아미노-3-클로로벤젠 · 3-클로로벤자민 · Orange GC base · M-CHLOROANILINE · 3-CHLOROBENZENAMINE

https://huagongshe.com/ko/chemical/7932

M-클로로아닐린 분자 구조식

식별자 및 물리적 특성

CAS No.108-42-9
분자식C6H6ClN
평균 분자량127.57 g/mol
단동위원소 질량127.01887687 g/mol
SMILESNc1cccc(Cl)c1
InChIKeyPNPCRKVUWYDDST-UHFFFAOYSA-N
PubChem CID7932
ChEMBLCHEMBL325415
ChEBICHEBI:229245
EC No.203-581-0
DTXSIDDTXSID0024761
현지명M-클로로아닐린

화학 및 물리적 성질

XLogP1.9
극성 표면적26
수소 결합 공여자 수1
수소 결합 수용자 수1
회전 가능 결합 수0
무거운 원자 수8
형식 전하0
복잡도74.9
물질 분류Nitrogen Compounds -> Amines, Aromatic
SpringerMaterials Properties13C nuclear magnetic resonance spectrum
LogP(분배 계수)log Kow = 1.881.9
냄새Characteristic sweet odor특유의 냄새
밀도1.216 at 68 °F (NTP, 1992) - Denser than waterwill sink1.2150 at 22 °C/4 °CRelative density (water = 1): 1.2161.206 g/mL at 25 °C(lit.)
Color/FormColorless to light amber, tends to darken during storage
용해도less than 1 mg/mL at 64 °F (NTP, 1992)Soluble in most common organic solventsMiscible in ethanol, ether, and acetoneIn water, 5,400 mg/L at 20 °CSolubility in water, g/100ml at 20 °C: 0.66.2g/L
인화점255 °F (NTP, 1992)118 °C c.c.
끓는 점446.9 °F at 760 mmHg (NTP, 1992)230.5 °C95-96 °C11 mm Hg(lit.)
DecompositionWhen heated to decomposition, it emits toxic fumes of /hydrogen chloride and nitrogen oxides/.230 °C
녹는점13.5 °F (NTP, 1992)-10.4 °C-10 °C−11-−9 °C(lit.)
증기 밀도4.41 (NTP, 1992) - Heavier than airwill sink (Relative to Air)Relative vapor density (air = 1): 4.4
증기압1 mm Hg ( 63.5 °C)
굴절률n20/D 1.594(lit.)
저장 조건Store below +30°C.
물리적 상태액체
pKa(산도 계수)3.46(at 25℃)
색상투명하고 연한 노란색에서 갈색까지
pH7.3 (H2O)(saturated aqueous solution)
용해도6.8g/L(20℃)
비열Cp(liquid): 1.56 J/(g·K), at 25℃
Merck14,2118
BRN605969
헨리 상수4.7×100 mol/(m3Pa) at 25℃, Chao et al. (2017)
유전율13.4(19℃)
안정성Material darkens in storage with no loss in purity, Material Darkens In Storage
InChI1S/C6H6ClN/c7-5-2-1-3-6(8)4-5/h1-4H,8H2
InChIKeyPNPCRKVUWYDDST-UHFFFAOYSA-N
SMILESNc1cccc(Cl)c1
LogP(분배 계수)0.77-2.03 at 25-30℃
NISTm-Chloroaniline(108-42-9)
EPAm-Chloroaniline (108-42-9)

화학적 성질

3-Chloroaniline is a clear pale yellow to brown liquid, which becomes darker during storage, insoluble in water, but soluble in ethanol, ether and acid solution.

안전 및 규제

GHS 분류DangerH301+H311 (25%): Toxic if swallowed or in contact with skin [Danger Acute toxicity, oralacute toxicity, dermal]P203, P260, P261, P262, P264, P264+P265, P270, P271, P272, P273, P280, P284, P301+P316, P302+P352, P304+P340, P305+P351+P338, P316, P318, P319, P320, P321, P330, P333+P317, P337+P317, P361+P364, P362+P364, P391, P403+P233, P405, and P501 (click each P-code to see the statement)Aggregated GHS information provided per 160 reports by companies from 15 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.H301: Toxic if swallowed [Danger Acute toxicity, oral]
규제 정보Chemical: Benzenamine, 3-chloro-Commission Regulation No 844/2012Benzenamine, 3-chloro- is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of Benzenamine, 3-chloro- 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)Status: Cease Manufacture Update: 07-11-2014 https://echa.europa.eu/registration-dossier/-/registered-dossier/68553-Chloroaniline: Does not have an individual approval but may be used under an appropriate group standard
운송 라벨(DOT)Poison
화재 위험This chemical is combustible. (NTP, 1992)Combustible. Gives off irritating or toxic fumes (or gases) in a fire.
건강 유해성SYMPTOMS: Symptoms of exposure to this chemical may include methemoglobinemia and, in large concentrations cyanosisdermatitis, liver and kidney damage, and death.
유해성 요약In the United Kingdom between 1961 and 1980, chloroaniline, p-toluidine, nitrobenzene, and nitrochlorobenzene were the most common industrial causes of methemoglobinemia. Dermal exposure was a more frequent route of toxicity than inhalation with these compounds. (Ellenhorn, M.J. and D.G. Barceloux. Medical Toxicology - Diagnosis and Treatment of Human Poisoning. New York, NY: Elsevier Science Publishing Co., Inc. 1988.) A skin and eye irritantCan induce methemoglobinemia[ICSC] Danger of skin sensitization[MAK]
반응성 그룹Aryl Halides
EC 분류Symbol: T, NR: 23/24/25-33-50/53S: (1/2)-28-36/37-45-60-61Note: C
UN 분류UN Hazard Class: 6.1UN Pack Group: II
Special ReportsSakamoto Y, Watanabe SBull Chem Soc Jpn 59 (10): 3033-8 (1986). The relation between chem structure and carcinogenicity was investigated in 38 polycyclic aromatic cmpd and 44 chlorinated aromatic hydrocarbons by means of (13)C-NMR.
TSCA 요건Pursuant to section 8(d) of TSCA, EPA promulgated a model Health and Safety Data Reporting Rule. The section 8(d) model rule requires manufacturers, importers, and processors of listed chemical substances and mixtures to submit to EPA copies and lists of unpublished health and safety studies. Benzenamine, 3-chloro- is included on this list.
Reactivity ProfileM-CHLOROANILINE is incompatible with acids, acid chlorides, acid anhydrides, chloroformates and strong oxidizing agents. (NTP, 1992)
대기 기준This action promulgates standards of performance for equipment leaks of Volatile Organic Compounds (VOC) in the Synthetic Organic Chemical Manufacturing Industry (SOCMI). The intended effect of these standards is to require all newly constructed, modified, and reconstructed SOCMI process units to use the best demonstrated system of continuous emission reduction for equipment leaks of VOC, considering costs, non air quality health and environmental impact and energy requirements. m-chloroaniline is produced, as an intermediate or a final product, by process units covered under this subpart.
소화Fires involving this compound can be controlled with a dry chemical, carbon dioxide or Halon extinguisher. (NTP, 1992)Use powder, AFFF, foam, carbon dioxide.
응급 조치Fresh air, rest. Artificial respiration may be needed. Refer for medical attention.Remove contaminated clothes. Rinse and then wash skin with water and soap. Refer for medical attention .First rinse with plenty of water for several minutes (remove contact lenses if easily possible), then refer for medical attention.Rinse mouth. Give one or two glasses of water to drink. Refer for medical attention .
응급 처치EYES: First check the victim for contact lenses and remove if present. Flush victim's eyes with water or normal saline solution for 20 to 30 minutes while simultaneously calling a hospital or poison control center. Do not put any ointments, oils, or medication in the victim's eyes without specific instructions from a physician. IMMEDIATELY transport the victim after flushing eyes to a hospital even if no symptoms (such as redness or irritation) develop.
안전 보관Separated from food and feedstuffs. Keep in the dark. Well closed.
노출 관리 및 개인 보호Biological Exposure Indices (BEI) [ACGIH] - Methemoglobin in blood = 1.5% of hemoglobin during or at end of shift. [ACGIH]
소화 절차Water, dry chemical, foam or carbon dioxide. /4-Chloroaniline/
비화재 누출 대응SMALL SPILLS AND LEAKAGE: If you spill this chemical, FIRST REMOVE ALL SOURCES OF IGNITION. Then, use absorbent paper to pick up all liquid spill material. Your contaminated clothing and absorbent paper should be sealed in a vapor-tight plastic bag for eventual disposal. Solvent wash all contaminated surfaces with 60-70% ethanol followed by washing with a soap and water solution. Do not reenter the contaminated area until the Safety Officer (or other responsible person) has verified that the area has been properly cleaned.
처리 방법SRP: The most favorable course of action is to use an alternative chemical product with less inherent propensity for occupational exposure or environmental contamination. Recycle any unused portion of the material for its approved use or return it to the manufacturer or supplier. Ultimate disposal of the chemical must consider: the material's impact on air qualitypotential migration in soil or watereffects on animal, aquatic, and plant lifeand conformance with environmental and public health regulations.
누출 처리Personal protection: chemical protection suit including self-contained breathing apparatus. Do NOT let this chemical enter the environment. Collect leaking and spilled liquid in sealable containers as far as possible. Absorb remaining liquid in sand or inert absorbent. Then store and dispose of according to local regulations.
Preventive MeasuresImmediately wash contaminated areas of body with concentrated soap solution. Remove contaminated clothing, dry, then wash with concentrated soap solution or dispose as waste. Contaminated shoes may be disposed of in an incinerator....Precaution should be taken to avoid inhalation of vapors.SRP: The scientific literature for the use of contact lenses in industry is conflicting. The benefit or detrimental effects of wearing contact lenses depend not only upon the substance, but also on factors including the form of the substance, characteristics and duration of the exposure, the uses of other eye protection equipment, and the hygiene of the lenses. However, there may be individual substances whose irritating or corrosive properties are such that the wearing of contact lenses would be harmful to the eye. In those specific cases, contact lenses should not be worn. In any event, the usual eye protection equipment should be worn even when contact lenses are in place.SRP: Contaminated protective clothing should be segregated in such a manner so that there is no direct personal contact by personnel who handle, dispose, or clean the clothing. Quality assurance to ascertain the completeness of the cleaning procedures should be implemented before the decontaminated protective clothing is returned for reuse by the workers. Contaminated clothing should not be taken home at end of shift, but should remain at employee's place of work for cleaning.
Isolation and EvacuationExcerpt from ERG Guide 152 [Substances - Toxic (Combustible)]:
Eye PreventionWear safety goggles or face shield.
생태독성 수치LC50 Eisenia andrei (Earthworm) 568-725 ug/L/14 daysLC50 Lumbricus rubellus (Earthworm) 388-469 ug/L/14 daysLC50 Poecilia reticulata (Guppy) 13 mg/L/14 days /Conditions of bioassay not specified in source examined/LC50 Crangon septemspinosa (Bay shrimp, Sand shrimp) 25 mg/L/96 hrrenewal, aerated sea water, 10 °CFor more Ecotoxicity Values (Complete) data for 3-CHLOROANILINE (9 total), please visit the HSDB record page.
환경 거동TERRESTRIAL FATE: Based on a classification scheme(1), an estimated Koc value of 250(SRC), determined from a log Kow of 1.88(2) and a regression-derived equation(3), indicates that 3-chloroaniline is expected to have moderate mobility in soil(SRC). However, aromatic amines are expected to bind strongly to humus or organic matter in soils due to the high reactivity of the aromatic amino group(4,5), suggesting that mobility may be much lower in some soils(SRC). 3-Chloroaniline may undergo covalent chemical bonding with humic materials which results in its chemical alteration and tight adsorption(6). There is evidence to suggest that this complexing may extend the residual life of these substances in soil for as much as 10 years(7). Due to this covalent bonding, significant leaching in soil systems is not generally expected to occur(SRC). The pKa of 3-chloroaniline is 3.52(10), indicating that this compound will primarily exist in its nonionic form in the environment. Volatilization of 3-chloroaniline from moist soil surfaces is expected to occur(SRC) given a Henry's Law constant of 1.0X10-6 atm-cu m/mole(8). However, adsorption to soil is expected to attenuate volatilization(SRC). 3-Chloroaniline is not expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure of 0.066 mm Hg(9). 3-Chloroaniline may degrade in soil by chemical and microbial processes(11). When 3-chloroaniline (30 ppm) was incubated in Guelph loam with water added to 60% water-holding capacity, levels declined rapidly for 2 weeks after which time the rate of loss decreased(11). The percent of 3-chlororaniline remaining in soil after 2 and 8 weeks were 38% and 18%, respectively(11).AQUATIC FATE: Based on a classification scheme(1), an estimated Koc value of 250(SRC), determined from a log Kow of 1.88(2) and a regression-derived equation(3), indicates that 3-chloroaniline may adsorb to suspended solids and sediment(SRC). In addition, 3-chloroaniline may undergo chemical bonding with humic materials in the water column and in the sediment(4). Volatilization from water surfaces is expected(3) based upon a Henry's Law constant of 1.0X10-6 atm-cu m/mole(5). Using this Henry's Law constant and an estimation method(3), volatilization half-lives for a model river and model lake are 42 and 310 days, respectively(SRC). However, aromatic amines are expected to bind strongly to humus or organic matter in soils due to the high reactivity of the aromatic amino group(13,14), and volatilization from water surfaces is expected to be attenuated by adsorption to suspended solids and sediment in the water column(SRC). The pKa of 3-chloroaniline is 3.52(6), indicating that this compound will primarily exist in its nonionic form in the environment. According to a classification scheme(7), measured BCF values ranging from 0.8 to 11.5(8,9) suggests the potential for bioconcentration in aquatic organisms is low(SRC). In a 3-day cultivation test using 2 different river waters from Japan and two different sea waters, 50% of initial 3-chloroaniline was degradedthe degradation was paralleled by growth of microbes(9,10). A biotransformation half-life of 0.4 year was determined for 3-chloroaniline in laboratory studies using two pond and one river water samples obtained near Athens, GA(12). Irradiation of an aqueous solution of 3-chloroaniline in a quartz tube with a fluorochemical lamp (wavelengths above 300 nm) resulted in a photodegradation half-life of 2.6 hours(14).ATMOSPHERIC FATE: According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere(1), 3-chloroaniline, which has a vapor pressure of 0.066 mm Hg at 25 °C(2), is expected to exist solely as a vapor in the ambient atmosphere. Vapor-phase 3-chloroaniline is degraded in the atmosphere by reaction with photochemically-produced hydroxyl radicals(SRC)the half-life for this reaction in air is estimated to be 5.1 hours(SRC), calculated from its rate constant of 7.6X10-11 cu cm/molecule-sec at 25 °C(SRC) that was derived using a structure estimation method(3). 3-Chloroaniline absorbs light with wavelengths >290 nm(4) and may be susceptible to direct photolysis by sunlight(SRC).
식품 조사 수치3-Chloroaniline was detected in several samples of potato peels, 0.18-0.36 ppb, from potatoes obtained from various geographic locations(1).
유해 작용Methemoglobinemia - The presence of increased methemoglobin in the bloodthe compound is classified as primary toxic effect.
노출 경로The substance can be absorbed into the body by inhalation, through the skin and by ingestion.
생태독성 발췌/AQUATIC SPECIES/ 21 day Daphnia reproduction tests were conducted in line with the provisional procedure proposed by the Federal Environmental Agency, as of Jan 1, 1984. Groups of 20, 24-hr old Daphnia magna Straus were exposed to 6.3 to 800 ug/L 3-chloroaniline in semi-static test vessels. Parent animals in the test and control vessels had to be pipetted 3 times/wk in freshly prepared test and control media at the corresponding concentration level. The no observed effect concentration (NOEC) was determined from the parameters of mortality of the parent animals, reproduction rate and appearance of the first offspring during the test period. In preliminary acute Daphnia tests, the 24 hr EC50 was 0.9 mg/L for 3-chloroaniline, the EC0 was 0.40 mg/L. The nominal 21 day no observed effect concn was 0.013 mg/L, with the more sensitive parameters being reproductive rate and the appearance of first offspring.
Plant Concentrations3-Chloroaniline, which is the main metabolite of chloropropham, corresponded to about 50% of the applied dosage of chloropropham in the 2nd of 3rd successive lettuce cultures(1). After the 3rd culture, the amount of chloropropham and 3-chloroaniline increased lettuce, as well as soil(1).
Signs and SymptomsBlue lips, fingernails and skin. Dizziness. Headache. Shortness of breath. Nausea. Vomiting. Convulsions. Weakness. Confusion. Unconsciousness.MAY BE ABSORBED! Redness. Burning sensation. Further see Inhalation.Redness. Pain.Abdominal pain. Further see Inhalation.
Ongoing Test StatusThe following link will take the user to the National Toxicology Program (NTP) Test Agent Search Results page, which tabulates all of the "Standard Toxicology & Carcinogenesis Studies", "Developmental Studies", and "Genetic Toxicity Studies" performed with this chemical. Clicking on the "Testing Status" link will take the user to the status (i.e., in review, in progress, in preparation, on test, completed, etc.) and results of all the studies that the NTP has done on this chemical. [http://ntp-apps.niehs.nih.gov/ntp_tox/index.cfm?fuseaction=ntpsearch.searchresults&searchterm=108-42-9]
Effluent ConcentrationsIn a comprehensive survey of wastewater from 4,000 industrial and publicly owned treatment works (POTWs) sponsored by the Effluent Guidelines Division of the U.S. EPA, 3-chloroaniline was identified in discharges of the following industrial category (positive occurrences, median concn in ug/L): organics and plastics (596.7), soaps and detergents (128.0), pharmaceuticals (658.7), organic chemicals (313.8), publicly owned treatment works (142.6)(3). The highest effluent concn was 612 ug/L in the pharmaceutical industry(3). Unspecified isomers of chloroaniline have been detected in the effluent from the publicly owned treatment works (POTW) of Sauget, IL(1). 3-Chloroaniline has been qualitatively detected in effluent water concentrates collected in 1974 and 1975 from advanced waste treatment facilities in Pomona, CA(2).
ICSC Environmental DataThe substance is toxic to aquatic organisms.
Soil Adsorption/MobilityThe Koc of 3-chloroaniline is estimated as 250(SRC), using a log Kow of 1.88(1) and a regression-derived equation(2). According to a classification scheme(3), this estimated Koc value suggests that 3-chloroaniline is expected to have moderate mobility in soil. However, aromatic amines are expected to bind strongly to humus or organic matter in soils due to the high reactivity of the aromatic amino group(4,5), suggesting that mobility may be much lower in some soils(SRC). In laboratory persistence studies using non-sterilized Hagerstown silty clay loam soil, 73% of applied 3-chloroaniline remained chemically bound to soil particles after 64 days of incubation(6). A related chemical, 2-chloroaniline, has been observed to undergo rapid and reversible covalent bonding with humic materials in aqueous solutionthe initial bonding reaction is followed by a slower and much less reversible reaction believed to represent the addition of the amine to quinoidal structures followed by oxidation of the product to give an amino-substituted quinone(7).
수질 위해 등급(WGK)2
TSCA 등재 상태TSCA listed
RTECS 번호BX0350000
운송 번호(UN)UN 2019 6.1/PG 2
독성LD50 orally in Rabbit: 256 mg/kg LD50 dermal Rat 250 mg/kg
관세 코드29214210
위험 문구(R)23/24/25-33-50/53
위험 표시T,N
안전 문구(S)28-36/37-45-60-61-28A
포장분류II
위험 등급6.1Acute Tox. 2 InhalationAcute Tox. 3 DermalAcute Tox. 3 OralAquatic Acute 1Aquatic Chronic 1Eye Irrit. 2Skin Sens. 1BSTOT RE 2 Oral
기존화학 물질KE-05524
F 고인화성물질8-10-23
위험 참고 사항Toxic
자연 발화 온도705 °C
저장 분류6.1A - Combustible acute toxic Cat. 1 and 2very toxic hazardous materials
유해 물질 데이터108-42-9(Hazardous Substances Data)
함량 및 규제정보물질구분: 유독물질혼합물(제품)함량정보: m-아미노클로로벤젠 및 이를 25% 이상 함유한 혼합물
유해화학물질 필터링97-1-448

용도

일반 설명

Colorless to light amber liquid with a sweet odor.

제조 및 합성 방법

제조 방법

3-Chloroaniline is obtained by reducing 3-Nitrochlorobenzene with iron powder in the presence of ferrous sulfate.