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Toluol-2-thiol

2-Thiocresol

HCID 8712
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Grundinformationen

CAS
137-06-4
Standard-SMILES
Cc1ccccc1S
InChIKey
LXUNZSDDXMPKLP-UHFFFAOYSA-N
Summenformel
C7H8S
Durchschnittliche Molmasse
124,21 g/mol
Monoisotopische Masse
124,03467126

Überblick

2-Methylbenzenethiol is a thiol.

Namen und Bezeichner

Bevorzugter Name
2-Thiocresol
IUPAC
2-methylbenzenethiol
Lokaler Name
Toluol-2-thiol
Englischer Name
2-Methylbenzenethiol
Summenformel
C7H8S
Molmasse
124.2

Namen und Synonyme

2-Methylbenzenethiolo-Toluenethiol137-06-4o-Thiocresol2-Methylthiophenol2-THIOCRESOL2-Toluenethiolo-Tolyl mercaptano-MercaptotolueneBenzenethiol, 2-methyl-o-Methylthiophenolo-Methylbenzenethiol
Weitere Namen anzeigen
FEMA 3240ortho-thiocresoluenethioLusafek-26762-THIOCRESOLE
Toluene-2-thiol2-Methylbenzene-1-thiol2-MethylphenylthiolTolylthiol, o-Tolylmercaptan, o-USAF EK-2676Toluene, 2-mercapto-FEMA No. 3240

Datenbank-Bezeichner

CAS
137-06-4
PubChem CID
8712
DTXSID
DTXSID8047135
ChEMBL
CHEMBL3182595
ChEBI
CHEBI:178255
UNII
6FU2EGI4VS
EC Number
205-276-8
Nikkaji
J5.627H

Eigenschaften

Berechnete StruktureigenschaftenWird ergänzt

XLogP
2,9
Polarare Oberfläche (TPSA)
1 Ų
H-Brücken-Donoren
1
H-Brücken-Akzeptoren
1
Frei drehbare Bindungen
0
Schwere Atome
8
Formalladung
0
Komplexität
70,8

Experimentelle und physikochemische Eigenschaften

Chemical ClassesOther Classes -> Sulfur Compounds
SpringerMaterials PropertiesBoiling point
FragrancesFragrance Ingredient (o-Toluenethiol) -> IFRA transparency List
LogP3.52
Food AdditivesFLAVORING AGENT OR ADJUVANT -> FDA Substance added to food
Density · 2 Einträge

1.041 @ 20 °C/4 °C

1.054-1.059

Flavoring AgentsEU Flavoring substances
Solubility · 2 Einträge

Sol in alcohol, ether; insol in water

(in ethanol)

Flash Point64 °C
Boiling Point · 3 Einträge

195 °C

194.00 to 196.00 °C. @ 760.00 mm Hg

Sicherheit und Regulatorisches

Sicherheitsangaben dienen nur zur Orientierung und ersetzen weder das Sicherheitsdatenblatt (SDB) des Lieferanten noch geltende Vorschriften oder eine fachliche Bewertung.

GHS-Klassifizierung

GHS Classification · 4 Einträge

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.

Gefahrenhinweise

Regulatory Information · 3 Einträge

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 · 1 Eintrag

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.

Flammable LimitsFlammable liquid.
Toxic Combustion ProductsWhen heated to decomp, it emits toxic fumes of /sulfur oxides/.
Hazard Classes and CategoriesAcute Tox. 4 (97%)

Sicherheit und Schutzausrüstung

Chemie und Industrie

Pharmakologische Informationen

Cellular LocationsMembrane

Verwendung und Herstellung

Uses · 4 Einträge

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 · 2 Einträge

(1977) NOT PRODUCED COMMERCIALLY IN USA

(1979) NOT PRODUCED COMMERCIALLY IN USA

Methods of ManufacturingREDUCTION OF TOLUENE-O-SULPHONYL WITH TIN AND HYDROCHLORIC ACID
Use Classification · 4 Einträge

Fragrance Ingredients

Flavoring Agents -> JECFA Flavorings Index

Flavouring Agent -> FLAVOURING_AGENT -> JECFA Functional Classes

Flavouring Agent -> FLAVOURING_AGENT -> JECFA Functional Classes

General Manufacturing InformationBenzenethiol, 2-methyl-: ACTIVE

Anwendungen

OccurrenceReported found in coffee

Verwenden2-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.

Vor- und nachgelagerte Produkte

Vorgelagerte Rohstoffe

Zugehörige Reaktionen

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Reaktionsgleichung von HRID 50966
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Reaktionsgleichung von HRID 161262
HRID 161262als EduktTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Reaktionsgleichung von HRID 172267
HRID 172267als EduktTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Reaktionsgleichung von HRID 209116
HRID 209116als EduktTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Reaktionsgleichung von HRID 215355
HRID 215355als EduktTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Reaktionsgleichung von HRID 233529
HRID 233529als Eduktuspto-grants-1997_01
Reaktionsgleichung von HRID 233558
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194-195 °C

DecompositionWhen heated to decomposition it emits toxic fumes of /sulfur oxides/.
Melting Point · 2 Einträge

15 °C

15 °C

Physikochemische Eigenschaften

Schmelzpunkt
10 · 10-12 °C(lit.)
Siedepunkt
195 °C · 195 °C(lit.)
Dichte
1.054 g/mL · 1.054 g/mL at 25 °C(lit.)
Brechungsindex
20 · n20/D 1.578(lit.)
FEMA
3240 · 3240 | O-TOLUENETHIOL
Flammpunkt
147 °F · 147 °F
storage temp.
30 °C · Store below +30°C.
Aggregatzustand
Liquid
pka
1 · pK1:6.64 (25°C)
Wichte
1.055 · 1.055
Farbe
Clear colorless to pale yellow
Geruch (Odor)
0.1 % · at 0.10 % in propylene glycol. meaty sulfurous onion garlic egg rubber
Geruchsart
meaty
Biologische Quelle
synthetic
Explosionsgrenze
1.1 % · 1.1%(V)
Wasserlöslichkeit
insoluble
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
CAS Datenbank
137 · 137-06-4(CAS DataBase Reference)
NIST chemische Informationen
2 · Benzenethiol, 2-methyl-(137-06-4)
EPA chemische Informationen
2 · Benzenethiol, 2-methyl- (137-06-4)
Disposal Methods · 1 Eintrag

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.

Toxikologische Informationen

Environmental Fate · 3 Einträge

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).

Adverse EffectsNeurotoxin - Other CNS neurotoxin
Soil Adsorption/Mobility · 1 Eintrag

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.

Artificial Pollution Sources2-Thiocresol's possible production as an antiseptic(1) may result in its release to the environment through various waste streams(SRC).
Environmental Bioconcentration · 1 Eintrag

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 · 1 Eintrag

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 · 1 Eintrag

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).

Probable Routes of Human ExposureOccupational exposure to 2-thiocresol may occur through inhalation and dermal contact with this compound at workplaces where 2-thiocresol is produced. (SRC)
Environmental Fate/Exposure Summary · 1 Eintrag

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)

Non-Human Toxicity ValuesLD50 Mouse ip 100 mg/kg

Sicherheitsdaten

wgk
3
tsca
TSCA listed
ridadr
2810
hs_code
29309090
RTECS-Nr.
XT8750000
risk_code
37/38-41-36/37/38-20/21/22
Toxizität
mouse,LD50,intraperitoneal,100mg/kg (100mg/kg),National Technical Information Service. Vol. AD277-689,
hazard_code
Xi,Xn
hazard_note
Harmful/Irritant/Stench
safety_code
26-39-36/37/39-23
hazard_class
6.1
packing_group
III
Speicherklasse
10 - Combustible liquids
Giftige Stoffe Daten
137-06-4(Hazardous Substances Data)
Hazard Classifications
Eye Irrit. 2Skin Irrit. 2STOT SE 3
Toluidin (o)Di-o-tolyldisulfid2-Methylbenzyl mercaptan, 97DimethyldisulfidPhenolChlortoluol (o)o-Kresol2-IodtoluolBenzo[b]thiophenCarbamimidothioic acid2-Bromtoluol

Nachgelagerte Produkte

Toluol-2-sulfonylchloridToluol-4-thiolToluol-2-sulfonamid4-Methyldibenzothiophene2,7-Dimethylbenzo[b]thiophene