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Benzylsulfonic acid

HCID 7532
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Grundinformationen

CAS
100-87-8
Standard-SMILES
O=S(=O)(O)Cc1ccccc1
InChIKey
NIXKBAZVOQAHGC-UHFFFAOYSA-N
Summenformel
C7H8O3S
Durchschnittliche Molmasse
172,2 g/mol
Monoisotopische Masse
172,01941512

Überblick

RN given refers to parent cpd

Namen und Bezeichner

Bevorzugter Name
Benzylsulfonic acid
IUPAC
phenylmethanesulfonic acid

Namen und Synonyme

Phenylmethanesulfonic acidBENZYLSULFONIC ACIDBenzenemethanesulfonic acidToluene-alpha-sulphonic acidalpha-Toluenesulfonic acidMethanesulfonic acid, phenyl-HSDB 5339EINECS 202-897-6UNII-5BRP81V98HBRN 2208420DTXSID2059221BENZYLSULFONIC ACID [HSDB]
Weitere Namen anzeigen
4-11-00-00485 (Beilstein Handbook Reference).ALPHA.-TOLUENESULFONIC ACIDBENZYL-.ALPHA.-SULFONIC ACIDTOLUENE-.ALPHA.-SULPHONIC ACIDalphaToluenesulfonic acidRefChem:119004Methanesulfonic acid, phenylDTXCID3032462

Datenbank-Bezeichner

CAS
100-87-8
PubChem CID
7532
DTXSID
DTXSID2059221
ChEMBL
CHEMBL1171433
UNII
5BRP81V98H
EC Number
202-897-6
Nikkaji
J182.139C

Eigenschaften

Berechnete Struktureigenschaften

XLogP
0,3
Polarare Oberfläche (TPSA)
62,8 Ų
H-Brücken-Donoren
1
H-Brücken-Akzeptoren
3
Frei drehbare Bindungen
2
Schwere Atome
11
Formalladung
0
Komplexität
196

Experimentelle und physikochemische Eigenschaften

Chemical ClassesOther Classes -> Organic Acids
DrugsPharmaceuticals -> Listed in ZINC15
CorrosivityTSA-94/30 LESS CORROSIVE TO STAINLESS STEEL THAN 75% H3PO4
Vapor Pressure0.0000034 [mmHg]
Stability/Shelf LifeTSA-94/30 WAS STABLE AGAINST CRYSTALLIZATION BELOW 50 °C

Sicherheit und Regulatorisches

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

Sicherheit und Schutzausrüstung

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 21(SRC), determined from a structure estimation method(2), indicates that benzylsulfonic acid is expected to have very high mobility in soil(SRC). Volatilization of benzylsulfonic acid from moist soil surfaces is not expected to be an important fate process(SRC) given an estimated Henry's Law constant of 1.0X10-9 atm-cu m/mole(SRC), using a fragment constant estimation method(3). Benzylsulfonic acid is not expected to volatilize from dry soil surfaces(SRC) based upon an estimated vapor pressure of 3.4X10-6 mm Hg(SRC), determined from a fragment constant method(4).

AQUATIC FATE: Based on a classification scheme(1), an estimated Koc value of 21(SRC), determined from an estimation method(2), indicates that benzylsulfonic acid is not expected to adsorb to suspended solids and sediment in water(SRC). Volatilization from water surfaces is not expected(3) based upon an estimated Henry's Law constant of 1.0X10-9 atm-cu m/mole(SRC), developed using a fragment constant estimation method(4). According to a classification scheme(5), an estimated BCF of 3(SRC), from an estimated log Kow of -0.67(6) and a regression-derived equation(7), suggests the potential for bioconcentration in aquatic organisms is low.

ATMOSPHERIC FATE: According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere(1), benzylsulfonic acid, which has an estimated vapor pressure of 3.4X10-6 mm Hg at 25 °C(SRC), determined from a fragment constant estimation method(2), will exist in both the vapor and particulate phases in the ambient atmosphere. Vapor-phase benzylsulfonic acid 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 65 hours(SRC), calculated from its rate constant of 6.0X10-12 cu cm/molecule-sec at 25 °C(SRC) determined using a structure estimation method(3). Particulate-phase benzylsulfonic acid may be removed from the air by wet and dry deposition(SRC).

Soil Adsorption/Mobility · 1 Eintrag

Using a structure estimation method based on molecular connectivity indices(1), the Koc for benzylsulfonic acid can be estimated to be 21(SRC). According to a classification scheme(2), this estimated Koc value suggests that benzylsulfonic acid is expected to have very high mobility in soil.

Environmental Bioconcentration · 1 Eintrag

An estimated BCF of 3 was calculated for benzylsulfonic acid(SRC), using an estimated log Kow of -0.67(1) and a regression-derived equation(2). According to a classification scheme(3), this BCF suggests the potential for bioconcentration in aquatic organisms is low.

Volatilization from Water/Soil · 1 Eintrag

The Henry's Law constant for benzylsulfonic acid is estimated as 1.0X10-9 atm-cu m/mole(SRC) using a fragment constant estimation method(1). This Henry's Law constant indicates that benzylsulfonic acid is expected to be essentially nonvolatile from water surfaces(2). Benzylsulfonic acid's Henry's Law constant(1) indicates that volatilization from moist soil surfaces will not occur(SRC). Benzylsulfonic acid is not expected to volatilize from dry soil surfaces(SRC) based upon an estimated vapor pressure of 3.4X10-6 mm Hg(SRC), determined from a fragment constant method(3).

Non-Human Toxicity Excerpts · 2 Einträge

MIXTURE OF 94% TOLUENESULFONIC ACID & 30% METHANOL (TSA-94/30) WAS LESS TOXIC THAN 75% H3PO4 IN ACUTE SKIN ABSORPTION TOXICITY, SKIN IRRITATION & EYE IRRITATION STUDIES IN RABBITS.

NO PERMANENT ILL EFFECTS WERE OBSERVED IN RATS WHICH INHALED TSA-94/30, & VAPORS WERE CONSIDERED ONLY SLIGHTLY TOXIC.

Environmental Abiotic Degradation · 1 Eintrag

The rate constant for the vapor-phase reaction of benzylsulfonic acid with photochemically-produced hydroxyl radicals has been estimated as 6.0X10-12 cu cm/molecule-sec at 25 °C(SRC) using a structure estimation method(1). This corresponds to an atmospheric half-life of about 65 hours at an atmospheric concentration of 5X10+5 hydroxyl radicals per cu cm(1).

Environmental Fate/Exposure Summary · 1 Eintrag

Benzylsulfonic acid has no reported statistics on production and use. If released to air, an estimated vapor pressure of 3.4X10-6 mm Hg at 25 °C indicates benzylsulfonic acid will exist in both the vapor and particulate phases in the ambient atmosphere. Vapor-phase benzylsulfonic acid 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 65 hrs. Particulate-phase benzylsulfonic acid will be removed from the atmosphere by wet and dry deposition. If released to soil, Benzylsulfonic acid is expected to have very high mobility based upon an estimated Koc of 21. Volatilization from moist soil surfaces is not expected to be an important fate process based upon an estimated Henry's Law constant of 1.0X10-9 atm-cu m/mole. Benzylsulfonic acid will not volatilize from dry soil surfaces based upon its vapor pressure. If released into water, Benzylsulfonic acid is not expected to adsorb to suspended solids and sediment in water based upon the estimated Koc. Volatilization from water surfaces is not expected to be an important fate process based upon this compound's estimated Henry's Law constant. An estimated BCF of 3 suggests the potential for bioconcentration in aquatic organisms is low. (SRC)

Chemie und Industrie

Pharmakologische Informationen

Metabolism/Metabolites · 2 Einträge

PHENYLTHIO & BENZYLTHIO RADICALS WERE OXIDIZED TO DIPHENYL & DIBENZYL DISULFIDE, BENZENESULFONIC ACID, BENZENEMETHANESULFONIC ACID & SULFURIC ACID AMONG OTHERS.

INEZIN WAS METABOLIZED TO TOLUENE-ALPHA-SULFONIC ACID BY MYCELIAL CELLS OF PIRICULARIA ORYZAE.

Verwendung und Herstellung

Uses · 2 Einträge

Used as a research chemical; No known commercial production in the US; [HSDB]

RESEARCH CHEMICAL

U.S. Production · 2 Einträge

(1979) NO EVIDENCE OF COMMERCIAL PRODN IN U.S.

(1981) NO EVIDENCE OF COMMERCIAL PRODN IN U.S.

Methods of ManufacturingPROBABLY BY REACTION OF HYDRAZINE HYDRATE WITH DIPHENYL METHIONATE, FOLLOWED BY DISTILLATION
General Manufacturing InformationBenzenemethanesulfonic acid: ACTIVE

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