Results for:
PubChem ID: 7811

4-methylbenzenethiol

Mass-Spectra

Compound Details

Synonymous names
Methylbenzenethiol
Methylthiophenol
paratoluenethiol
p-Methylphenylmercaptan
p-Methylbenzenethiol
p-Methylbenzenthiol
Thiocresol
4-Methylphenylmercaptan
p-Mercaptotoluene
p-Methylthiophenol
p-Tolylthiophenol
WLHCBQAPPJAULW-UHFFFAOYSA-N
4-Methylbenzenethiol
p-Methylphenyl mercaptan
p-tolylmercaptan
4-Methylthiophenol
p-Thiolcresol
p-Toluenethiol
x-Toluenethiol
4-Mercaptotoluene
p-Thiocresol
p-Tolylthiol
4-Methylphenyl mercaptan
4-Toluenethiol
p-mercapto-toluene
p-methyl thiophenol
4-Methyl-benzenethiol
4-methylbenzene thiol
4-THIOCRESOL
AC1L1PLR
p-Tolyl mercaptan
4-methyl-benzenethio
4-methyl-thiophenol
4-methylthio-phenol
4-mercapto-toluen
4-mercapto-toluene
6L2WW9XYZO
Thio-p-cresol
AC1Q2MZ1
Toluene-4-thiol
benzenethiol,4-methyl-
PubChem6809
UNII-6L2WW9XYZO
1-Mercapto-4-methylbenzene
KSC175K5B
M833
UNII-11GBT0K4HR component WLHCBQAPPJAULW-UHFFFAOYSA-N
4-methylbenzene-1-thiol
NSC2227
SCHEMBL72612
thiocresol, p-
CTK0H5550
X4833
4-Methylbenzenethiol, 98%
ACMC-2098jt
Benzenethiol, 4-methyl-
CHEMBL119359
RP19605
STR00880
ar-Toluenethiol (8CI)
HSDB 2024
PHENYLTHIO, 4-METHYL-
AK162882
DTXSID5048188
Jsp000583
NSC 2227
NSC-2227
NSC229565
OR019881
OR198631
OR198632
OR250305
OR256296
PS-5132
Toluene, 4-mercapto-
USAF EK-510
WLN: SHR D1
ANW-15351
BP-12556
CJ-16033
DSSTox_GSID_48188
NSC 41898
SC-00251
TL8006744
DSSTox_CID_28163
DSSTox_RID_82724
MFCD00004851
ZINC19230140
AI3-09056
AI3-25191
KB-204526
LS-154205
LT03330196
NSC-229565
RTR-001261
ST24043913
TR-001261
AKOS000120273
Benzenethiol, methyl- (9CI)
I09-0900
J-001595
J-512887
BRN 0605761
FT-0619525
Tox21_303614
106-45-6
F0001-0122
MCULE-7745246721
NCGC00257443-01
CAS-106-45-6
EINECS 203-399-1
26445-03-4
MolPort-000-157-563
65206-EP2270114A1
65206-EP2305648A1
65206-EP2308812A2
86384-EP2269978A2
86384-EP2269985A2
86384-EP2269991A2
86384-EP2284150A2
86384-EP2284151A2
86384-EP2284152A2
86384-EP2284153A2
86384-EP2284155A2
86384-EP2284156A2
86384-EP2284164A2
86384-EP2287140A2
86384-EP2287148A2
86384-EP2287150A2
86384-EP2295419A2
86384-EP2305637A2
4-06-00-02153 (Beilstein Handbook Reference)
InChI=1/C7H8S/c1-6-2-4-7(8)5-3-6/h2-5,8H,1H
Microorganism:

Yes

IUPAC name4-methylbenzenethiol
SMILESCC1=CC=C(C=C1)S
InchiInChI=1S/C7H8S/c1-6-2-4-7(8)5-3-6/h2-5,8H,1H3
FormulaC7H8S
PubChem ID7811
Molweight124.2
LogP2.58
Atoms16
Bonds16
H-bond Acceptor0
H-bond Donor1
Chemical ClassificationBenzenoids Thiols

mVOC Specific Details

Boiling Point
DegreeReference
195 deg C @ 760 mm HgBudavari, S. (ed.). The Merck Index - An Encyclopedia of Chemicals, Drugs, and Biologicals. Whitehouse Station, NJ: Merck and Co., Inc., 1996., p. 1591
Volatilization
The Henry's Law constant for 4-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 4-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 6.82(3) for 4-thiocresol indicates that the anionic form of 4-thiocresol will exist in slightly acidic to basic waters and the anionic form is not expected to volatilize from water(SRC). 4-Thiocresol's Henry's Law constant(1) indicates that volatilization of the neutral species from moist soil surfaces may occur(SRC). However, 4-thiocresol in the anionic form is not expected to volatilize. 4-Thiocresol is not expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure of 0.807 mm Hg(4).
Literature: (1) Meylan WM, Howard PH; Environ Toxicol Chem 10: 1283-93 (1991) (2) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 15-1 to 15-29 (1990) (3) Serjeant, E.P., Dempsey B.; Ionisation Constants of Organic Acids in Aqueous Solution. International Union of Pure and Applied Chemistry (IUPAC). IUPAC Chemical Data Series No. 23. NY, NY: Pergamon Press, Inc. p. 279 (1979) (4) Dykyj J, Repas M; Petrochemia 18: 179-98 (1973)
Solubility
Insol in water; sol in alcohol, ether
Literature: Budavari, S. (ed.). The Merck Index - An Encyclopedia of Chemicals, Drugs, and Biologicals. Whitehouse Station, NJ: Merck and Co., Inc., 1996., p. 1591
Soil Adsorption
Using a structure estimation method based on molecular connectivity indices(1), the Koc for 4-thiocresol can be estimated to be 430(SRC). According to a classification scheme(2), this estimated Koc value suggests that 4-thiocresol is expected to have moderate mobility in soil. The pKa of 4-thiocresol is 6.82(3) indicating that the anionic form of 4-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.
Literature: (1) Meylan WM et al; Environ Sci Technol 26: 1560-67 (1992) (2) Swann RL et al; Res Rev 85: 17-28 (1983) (3) Serjeant EP, Dempsey B; Ionisation Constants of Organic Acids in Aqueous Solution. International Union of Pure and Applied Chemistry (IUPAC). IUPAC Chemical Data Series No. 23. NY, NY: Pergamon Press, Inc. p. 279 (1979)
Vapor Pressure
PressureReference
0.807 mm Hg @ 25 deg CDykyj J, Repas M; Petrochemia 18: 179-98 (1973)

Microorganisms emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
BacteriaCarnobacterium Divergens 9Pn/aErcolini et al., 2009
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
BacteriaCarnobacterium Divergens 9Pn/an/a