기본 정보
- 표준 SMILES
Cc1ccccc1S- InChIKey
LXUNZSDDXMPKLP-UHFFFAOYSA-N- 분자식
- C7H8S
- 평균 분자량
- 124.21 g/mol
- 단동위원소 질량
- 124.03467126
개요
2-Methylbenzenethiol is a thiol.
이름 및 식별자
- 우선 이름
- 2-Thiocresol
- IUPAC
- 2-methylbenzenethiol
- 영어명
- 2-Methylbenzenethiol
- 분자식
- C7H8S
- 분자량
- 124.2
이름 및 동의어
이름 더 보기
데이터베이스 식별자
- CAS
137-06-4- PubChem CID
- 8712
- DTXSID
DTXSID8047135- ChEMBL
CHEMBL3182595- ChEBI
CHEBI:178255- UNII
- 6FU2EGI4VS
- EC Number
- 205-276-8
- Nikkaji
- J5.627H
물성
구조 계산 물성
- XLogP
- 2.9
- 극성 표면적
- 1 Ų
- 수소 결합 공여자 수
- 1
- 수소 결합 수용자 수
- 1
- 회전 가능 결합 수
- 0
- 무거운 원자 수
- 8
- 형식 전하
- 0
- 복잡도
- 70.8
실험 및 물리화학적 성질
Density
1.041 @ 20 °C/4 °C
1.054-1.059
Solubility
Sol in alcohol, ether; insol in water
(in ethanol)
Boiling Point
195 °C
194.00 to 196.00 °C. @ 760.00 mm Hg
194-195 °C
Melting Point
15 °C
15 °C
물리화학적 성질
- 녹는점
- 10 · 10-12 °C(lit.)
- 끓는 점
- 195 °C · 195 °C(lit.)
- 밀도
- 1.054 g/mL · 1.054 g/mL at 25 °C(lit.)
- 굴절률
- 20 · n20/D 1.578(lit.)
- FEMA
- 3240 · 3240 | O-TOLUENETHIOL
- 인화점
- 147 °F · 147 °F
- 저장 조건
- 30 °C · Store below +30°C.
- 물리적 상태
- 액체
- 산도 계수 (pKa)
- 1 · pK1:6.64 (25°C)
- Specific Gravity
- 1.055 · 1.055
- 색상
- 무색~담황색 투명
- 냄새
- 0.1 % · 프로필렌 글리콜 중 0.10%. 고기가 많은 유황 양파 마늘 계란 고무
- 냄새 유형
- 고기가 많은
- 생물학적 소스
- synthetic
- 폭발한계
- 1.1 % · 1.1%(V)
- 수용성
- 불용성
- Merck
- 14 · 14,9325
- JECFA Number
- 528 · 528
- BRN
- 774068 · 774068
- Henry's Law Constant
- 2.7 · 2.7×10-2 mol/(m3Pa) at 25℃, HSDB (2015)
- InChI
- 1S/C7H8S/c1-6-4-2-3-5-7(6)8/h2-5,8H,1H3
- InChIKey
- LXUNZSDDXMPKLP-UHFFFAOYSA-N
- SMILES
- Cc1ccccc1S
- LogP
- 2.98 · 2.98
- NIST
- 2 · Benzenethiol, 2-methyl-(137-06-4)
- EPA
- 2 · Benzenethiol, 2-methyl- (137-06-4)
화학적 성질
CLEAR COLOURLESS TO SLIGHTY YELLOW-BROWN LIQUID
안전 및 규제
GHS 분류
GHS Classification
Danger
H302 (97%): Harmful if swallowed [Warning Acute toxicity, oral]
P260, P264, P270, P280, P301+P317, P301+P330+P331, P302+P361+P354, P304+P340, P305+P354+P338, P316, P321, P330, P363, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 1454 reports by companies from 13 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
유해성 정보
Regulatory Information
Chemical: Benzenethiol, 2-methyl-
Regulation (EC) No 1831/2003 (amended)
Benzenethiol, 2-methyl-: Does not have an individual approval but may be used under an appropriate group standard
Hazards Summary
Emergency treatment: Ortho-cresol; o-Cresol is corrosive to tissues; After absorption by any route, it can cause CNS depression, respiratory failure, seizures, methemoglobinemia, hemolytic anemia, and liver and kidney damage; [HSDB] A severe skin, eye, and respiratory tract irritant; Inhalation of high concentrations may cause CNS depression and pulmonary edema; [CHEMINFO] Safe when used as a flavoring agent in food; [JECFA] An irritant; Inhalation may cause CNS effects (strong odor will minimize inhalation exposure); [Alfa Aesar MSDS] See Cresol, all isomers.
안전 및 보호
Disposal Methods
SRP: At the time of review, criteria for land treatment or burial (sanitary landfill) disposal practices are subject to significant revision. Prior to implementing land disposal of waste residue (including waste sludge), consult with environmental regulatory agencies for guidance on acceptable disposal practices.
독성 정보
Environmental Fate
TERRESTRIAL FATE: Based on a classification scheme(1), an estimated Koc value of 440(SRC), determined from a structure estimation method(2), indicates that 2-thiocresol is expected to have moderate mobility in soil(SRC). The pKa of 2-thiocresol is 6.64(3) indicating that the anionic form of 2-thiocresol will exist in slightly acidic to basic soils and anions are expected to have higher mobility than the neutral species(SRC). Volatilization of 2-thiocresol from moist soil surfaces is expected to be an important fate process(SRC) given an estimated Henry's Law constant of 3.6X10-4 atm-cu m/mole(SRC), using a fragment constant estimation method(4). However, 2-thiocresol in the anionic form will not volatilize. 2-Thiocresol is not expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure of 0.816 mm Hg(5).
AQUATIC FATE: Based on a classification scheme(1), an estimated Koc value of 440(SRC), determined from an estimation method(2), indicates that 2-thiocresol is expected to slightly adsorb to suspended solids and sediment(SRC). Volatilization of the neutral species from water surfaces is expected(3) based upon an estimated Henry's Law constant of 3.6X10-4 atm-cu m/mole(SRC), developed using a fragment constant estimation method(4). Using this Henry's Law constant and an estimation method(3), volatilization half-lives for a model river and model lake are 3 hrs and 5.2 days, respectively(SRC). A pKa of 6.64(5) indicates that the anionic form of 2-thiocresol will exist in slightly acidic to basic waters and the anionic form will not volatilize from water(SRC). According to a classification scheme(6), an estimated BCF of 62(SRC), from an estimated log Kow of 3.2(7) and a regression-derived equation(8), suggests the potential for bioconcentration in aquatic organisms is moderate.
ATMOSPHERIC FATE: According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere(1), 2-thiocresol, which has a vapor pressure of 0.816 mm Hg at 25 °C(2), is expected to exist solely in the vapor-phase in the ambient atmosphere. Vapor- phase 2-thiocresol 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 27 hrs(SRC), calculated from its rate constant of 1.4X10-11 cu cm/molecule-sec at 25 °C(SRC) determined using a structure estimation method(3). Although thiocresols may be susceptible to photolysis, sufficient experimental data are not available to predict the relative importance of their photolysis in the environment(SRC).
Soil Adsorption/Mobility
Using a structure estimation method based on molecular connectivity indices(1), the Koc for 2-thiocresol can be estimated to be 440(SRC). According to a classification scheme(2), this estimated Koc value suggests that 2-thiocresol is expected to have moderate mobility in soil. The pKa of 2-thiocresol is 6.64(3) indicating that the anionic form of 2-thiocresol will exist in slightly acidic to basic soils and anions are expected to have higher mobility than the neutral species(SRC). Volatilization from moist soil surfaces is not expected to be an important fate process for the anionic species.
Environmental Bioconcentration
An estimated BCF of 62 was calculated for 2-thiocresol(SRC), using an estimated log Kow of 3.2(1) and a regression-derived equation(2). According to a classification scheme(3), this BCF suggests the potential for bioconcentration in aquatic organisms is moderate.
Volatilization from Water/Soil
The Henry's Law constant for 2-thiocresol is estimated as 3.6X10-4 atm-cu m/mole(SRC) using a fragment constant estimation method(1). This Henry's Law constant indicates that 2-thiocresol is expected to volatilize from water surfaces(2). Based on this Henry's Law constant, the volatilization half-life of the neutral species from a model river (1 m deep, flowing 1 m/sec, wind velocity of 3 m/sec)(2) is estimated as 3 hrs(SRC). The volatilization half-life of the neutral species from a model lake (1 m deep, flowing 0.05 m/sec, wind velocity of 0.5 m/sec)(2) is estimated as 5.2 days(SRC). A pKa of 6.64(3) for 2-thiocresol indicates that the anionic form of 2-thiocresol will exist in slightly acidic to basic waters and the anionic form is not expected to volatilize from water(SRC). 2-Thiocresol's Henry's Law constant(1) indicates that volatilization of the neutral species from moist soil surfaces may occur(SRC). However, 2-thiocresol in the anionic form is not expected to volatilize. 2-Thiocresol is not expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure of 0.816 mm Hg(4).
Environmental Abiotic Degradation
The rate constant for the vapor-phase reaction of 2-thiocresol with photochemically-produced hydroxyl radicals has been estimated as 1.4X10-11 cu cm/molecule-sec at 25 °C(SRC) using a structure estimation method(1). This corresponds to an atmospheric half- life of about 27 hrs at an atmospheric concentration of 5X10+5 hydroxyl radicals per cu cm(1). 2-Thiocresol is not expected to undergo hydrolysis in the environment due to the lack of hydrolyzable functional groups(2). Although thiocresols may be susceptible to photolysis, sufficient experimental data are not available to predict the relative importance of their photolysis in the environment(SRC).
Environmental Fate/Exposure Summary
2-Thiocresol's possible production as an antiseptic and as a bleach in the manufacture of latex may result in its release to the environment through various waste streams. If released to air, a vapor pressure of 0.816 mm Hg at 25 °C indicates 2-thiocresol will exist solely in the vapor phase in the ambient atmosphere. Vapor-phase 2-thiocresol will be degraded in the atmosphere by reaction with photochemically-produced hydroxyl radicals; the half-life for this reaction in air is estimated to be 27 hrs. Although thiocresols may be susceptible to photolysis, sufficient experimental data are not available to predict the relative importance of their photolysis in the environment. If released to soil, 2-thiocresol is expected to have moderate mobility based upon an estimated Koc of 440. The pKa of 2-thiocresol is 6.64 indicating that the anionic form of 2-thiocresol will exist in slightly acidic to basic soils and these anions are expected to have higher mobility than the neutral species. Volatilization of the neutral species from moist soil surfaces is expected to be an important fate process based upon an estimated Henry's Law constant of 3.6X10-4 atm-cu m/mole. However, volatilization of the anionic species from moist soil surfaces does not occur. 2-Thiocresol is not expected to volatilize from dry soil surfaces based upon its vapor pressure. If released into water, 2-thiocresol is expected to slightly adsorb to suspended solids and sediment based upon the estimated Koc. Volatilization of the neutral species from water surfaces is expected to be an important fate process based upon this compound's estimated Henry's Law constant. However, based on the pKa, the anionic form of 2-thiocresol will exist in slightly acidic to basic waters and the anionic form does not volatilize from water. Estimated volatilization half-lives of the neutral species for a model river and model lake are 3 hrs and 5.2 days, respectively. An estimated BCF of 62 suggests the potential for bioconcentration in aquatic organisms is moderate. Hydrolysis is not expected to occur due to the lack of hydrolyzable functional groups. Occupational exposure to 2-thiocresol may occur through inhalation and dermal contact with this compound at workplaces where 2-thiocresol is produced or used. (SRC)
안전 데이터
- wgk
- 3
- tsca
- TSCA listed
- rtecs
- XT8750000
- ridadr
- 2810
- 독성
- mouse,LD50,intraperitoneal,100mg/kg (100mg/kg),National Technical Information Service. Vol. AD277-689,
- HS 번호
- 29309090
- risk_code
- 37/38-41-36/37/38-20/21/22
- hazard_code
- Xi,Xn
- safety_code
- 26-39-36/37/39-23
- 포장분류
- III
- 위험 등급
- 6.1
- 위험 참고 사항
- Harmful/Irritant/Stench
- Hazard Classifications
- Eye Irrit. 2Skin Irrit. 2STOT SE 3
- 스토리지 클래스
- 10 - Combustible liquids
- 유해 물질 데이터
- 137-06-4(Hazardous Substances Data)
화학 및 산업
약리 정보
용도 및 제조
Uses
Used as a bleach in latex manufacturing, an antiseptic, and a dermatologic agent; [HSDB] Used as an intermediate in the manufacture of chemicals; [CHEMINFO] Used as flavoring agent; [JECFA]
Using Disinfectants or Biocides [Category: Clean]
Antiseptic; dermatologic /unspecified isomer/
As a bleach in the manufacture of latex /tolyl mercaptan, isomer not stated/
U.S. Production
(1977) NOT PRODUCED COMMERCIALLY IN USA
(1979) NOT PRODUCED COMMERCIALLY IN USA
Use Classification
Fragrance Ingredients
Flavoring Agents -> JECFA Flavorings Index
Flavouring Agent -> FLAVOURING_AGENT -> JECFA Functional Classes
Flavouring Agent -> FLAVOURING_AGENT -> JECFA Functional Classes
응용 분야
출처Reported found in coffee
용도2-Thiocresol performs a fungicidal and inhibitory activity against Histoplasma capsulatum. Reagent for molecular modeling and preparation of 4-hydroxy-5,6-dihydropyrones as inhibitors of HIV protease.
상·하류 제품 정보
상류 원료
하류 제품
공급사50 곳
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