Ethanthiol
ETHYL MERCAPTAN · C2H5SH · Ethanthiol · Thioethanol · MERCAPTAN C2 · 1-ETHANETHIOL · Ethylmerkaptan · EM RT

Identifikatoren & physikalische Daten
| CAS No. | 75-08-1 |
|---|---|
| Summenformel | C2H6S |
| Durchschnittliche Molmasse | 62,14 g/mol |
| Monoisotopische Masse | 62,01902119 g/mol |
| SMILES | CCS |
| InChIKey | DNJIEGIFACGWOD-UHFFFAOYSA-N |
| PubChem CID | 6343 |
| ChEBI | CHEBI:46511 |
| EC No. | 200-837-3 |
| DTXSID | DTXSID9026394 |
| Lokaler Name | Ethanthiol |
Chemische & physikalische Eigenschaften
| XLogP | 0,9 |
|---|---|
| Polarare Oberfläche (TPSA) | 1 |
| H-Brücken-Donoren | 1 |
| H-Brücken-Akzeptoren | 1 |
| Frei drehbare Bindungen | 0 |
| Schwere Atome | 3 |
| Formalladung | 0 |
| Komplexität | 2,8 |
| Stoffklassen | Other Classes -> ThiolsFlammable agents - 4th degree |
| SpringerMaterials Properties | Schoenflies notation |
| Pestizide | RodenticidesActive substance -> EU Pesticides database: Not approved |
| LogP (Verteilungskoeffizient) | 1.5 |
| Geruch | Leek-like odorPenetrating garlic-like odorStrong, skunk-like odor. |
| Lebensmittelzusatzstoffe | FLAVORING AGENT OR ADJUVANT -> FDA Substance added to food |
| Dichte | 0.826 at 68 °F (USCG, 1999) - Less dense than waterwill float0.8315 at 25 °C/4 °CRelative density (water = 1): 0.8390.833-0.8390.8315 @25 °C0.839 g/mL at 25 °C(lit.) |
| Aromastoffe | EU Flavoring substances |
| Viscosity | 0.003155 g/cm sec at 20 °C |
| Color/Form | Colorless liquid [Note: A gas above 95 degrees F]. |
| Löslichkeit | 0.7 % (NIOSH, 2024)Soluble in alcohol, ether, petroleum naphthaSoluble in acetone, dilute alkaliIn water, 15,603 mg/L at 25 °CSolubility in water, g/100ml at 20 °C: 0.68Slightly soluble in waterSoluble in Ether, Alcohol, AcetoneSlightly miscible with water. |
| Flammpunkt | less than 0 °F (USCG, 1999)-48.3 C-48.3 °C (Closed cup)-54 °C (Closed cup)-55 °F1 °F |
| Schmelzpunkt | -148 °C |
| Siedepunkt | 35 °C(lit.) |
| Dampfdichte | 2.1 (vs air) |
| Dampfdruck | 8.51 psi ( 20 °C) |
| Brechungsindex | n20/D 1.4306(lit.) |
| FEMA | 4258 | ETHANETHIOL |
| Lagerbedingungen | Store below +30°C. |
| Aggregatzustand | Liquid |
| pKa (Säurekonstante) | 10.6(at 25℃) |
| Farbe | Colorless |
| Geruch | Strong chunkoffensive garlic. |
| Biologische Quelle | synthetic |
| Explosionsgrenze | 2.8-18%(V) |
| Geruchsschwelle | 0.0000087ppm |
| Spezifische Wärmekapazität | Cp(liquid): 1.9 J/(g·K)Cp(gas): 1.17 J/(g·K), at 25℃ |
| JECFA Number | 1659 |
| Merck | 14,3726 |
| BRN | 773638 |
| Henry-Konstante | 3.57(x 10-3 atmm3/mol) at 25 °C (Przyjazny et al., 1983) |
| Dielektrizitätskonstante | 6.9(14℃) |
| Stabilität | Stable. Extremely flammable - note low flash point. Incompatible with oxidizing agents, strong acids. May form explosive mixtures with air. |
| Hauptanwendungen | cleaning productscosmeticsflavors and fragrancesfood and beveragespersonal care |
| InChI | 1S/C2H6S/c1-2-3/h3H,2H2,1H3 |
| InChIKey | DNJIEGIFACGWOD-UHFFFAOYSA-N |
| SMILES | CCS |
| LogP (Verteilungskoeffizient) | 1.44 |
| CAS Datenbank | 75-08-1(CAS DataBase Reference) |
| NIST chemische Informationen | Ethanethiol(75-08-1) |
| EPA chemische Informationen | Ethyl mercaptan (75-08-1) |
Sicherheit & Vorschriften
| GHS-Einstufung | DangerH224: Extremely flammable liquid and vapor [Danger Flammable liquids]P210, P233, P240, P241, P242, P243, P261, P264, P270, P271, P273, P280, P301+P317, P303+P361+P353, P304+P340, P316, P321, P330, P370+P378, P391, P403+P233, P403+P235, P405, and P501 (click each P-code to see the statement)H225 (93.1%): Highly Flammable liquid and vapor [Danger Flammable liquids]P210, P233, P240, P241, P242, P243, P261, P264, P270, P271, P273, P280, P301+P317, P303+P361+P353, P304+P340, P317, P330, P370+P378, P391, P403+P235, and P501 (click each P-code to see the statement) |
|---|---|
| Regulatorische Informationen | Chemical: EthanethiolCommission Regulation (EC) No 1565/2000 (Repealed by Com. Implementing Reg. (EU) No 872/2012)Ethanethiol is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of Ethanethiol 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: Active Update: 16-02-2018 https://echa.europa.eu/registration-dossier/-/registered-dossier/2123Ethanethiol: HSNO Approval: HSR001043 Approved with controlsThe New Jersey Worker and Community Right to Know Act requires public and private employers to provide information about hazardous substances at their workplaces. (N.J.S.A. 34:5A-1 et. seq.) |
| DOT-Kennzeichnung | Flammable Liquid |
| Brandgefahren | Special Hazards of Combustion Products: Irritating fumes of sulfur dioxide are generated.· HIGHLY FLAMMABLE: Will be easily ignited by heat, sparks or flames.Extremely flammable. Gives off irritating or toxic fumes (or gases) in a fire. Vapour/air mixtures are explosive. |
| Brandpotenzial | Dangerous, when exposed to heat or flame or oxidizers.Minimum ignition temperature in air: 299 °Cin oxygen: 261 °CCan react vigorously with oxidizing materials.Extremely flammable. |
| Gesundheitsgefahren | Inhalation of vapor causes muscular weakness, convulsions, respiratory paralysis. High concentrations may cause pulmonary irritation. Liquid irritates eyes and skin. Ingestion causes nausea and irritation of mouth and stomach. (USCG, 1999) |
Anwendungen & Verwendung
Beschreibung
Ethane thiol, commonly known as ethyl mercaptan, is a colorless gas or clear liquid with a distinct odor. It is an organosulfur compound with the formula CH3CH2SH. Abbreviated EtSH, it consists of an ethyl group (Et), CH3CH2, attached to a thiol group, SH. Its structure parallels that of ethanol, but with S instead of O. The odor of EtSH is infamous. Ethanethiol is more volatile than ethanol due to a diminished ability to engage in hydrogen bonding. Ethanethiol is toxic. It occurs naturally as a minor component of petroleum, and may be added to other wise odorless gaseous products such as liquefied petroleum gas (LPG) to help warn of gas leaks. At these concentrations, ethanethiol is not harmful.
Verwenden
Ethanethiol is used as an intermediate inthe manufacture of insecticides, plastics, andantioxidants; and as an additive to natural gasto give odor. It occurs in illuminating gas andin petroleum distillates.
Herstellung & Synthese
synthetische
Ethanethiol is prepared by the reaction of ethylene with hydrogen sulfide over a catalyst. The various producers utilize different catalysts in this process. It is also be prepared commercially by the reaction of ethanol with hydrogen sulfide gas over an acidic solid catalyst, such as alumina. Ethanethiol was originally reported by Zeiss in 1834 . Zeise treated calcium ethyl sulfate with a suspension of barium sulfide saturated with hydrogen sulfide. He is credited with naming the C2H5S- group as mercaptum. Ethanethiol can also be prepared by a halide displacement reaction, where ethyl halide is reacted with aqueous sodium bisulfide. This conversion was demonstrated as early as 1840 by Henri Victor Regnault.