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HCID 8404Erstellt: 24. Oktober 2026

1,2,3,4-Tetrahydronaphthalin

TETRALIN · TETRALINE · TETRAHYDRONAPHTHALENE · Naphthalene, 1,2,3,4-tetrahydro- · THN · 1,2,3,4-tetrahydro-naphthalen · TETRANAP · Tetralina

https://huagongshe.com/de/chemical/8404

Molekülstruktur von 1,2,3,4-Tetrahydronaphthalin

Identifikatoren & physikalische Daten

CAS No.119-64-2
SummenformelC10H12
Durchschnittliche Molmasse132,2 g/mol
Monoisotopische Masse132,09390038 g/mol
SMILESc1ccc2c(c1)CCCC2
InChIKeyCXWXQJXEFPUFDZ-UHFFFAOYSA-N
PubChem CID8404
ChEMBLCHEMBL1575635
ChEBICHEBI:35008
EC No.204-340-2
DTXSIDDTXSID1026118
Lokaler Name1,2,3,4-Tetrahydronaphthalin

Chemische & physikalische Eigenschaften

XLogP3,5
Polarare Oberfläche (TPSA)0
H-Brücken-Donoren0
H-Brücken-Akzeptoren0
Frei drehbare Bindungen0
Schwere Atome10
Formalladung0
Komplexität92,6
StoffklassenOther Classes -> NaphthalenesVolatile Organic Compound (VOC)
pHACIDITY NEUTRAL
SpringerMaterials Properties13C nuclear magnetic resonance spectrum
LogP (Verteilungskoeffizient)3.783.49
GeruchODOR RESEMBLING MIXTURE OF BENZENE & MENTHOLMOLDY, TURPENTINE ODORPungent odor
Dichte0.974 at 68 °F (liquid (USCG, 1999) - Less dense than waterwill float0.9702 G/ML @ 20 °C/4 °CMOISTURE CONTENT NONERESIDUE ON EVAPORATION NONEBULK DENSITY 8 LB/GALRelative density (water = 1): 0.97020.981 @25 °C0.973 g/mL at 25 °C (lit.)
Viscosity2.012 cP @ 25 °C
Color/FormCOLORLESS LIQUID
LöslichkeitMISCIBLE WITH ETHANOL, BUTANOL, ACETONE, BENZENE, PETROLEUM ETHER, CHLOROFORM, &PETROLEUM ETHER, DECALINSOL IN METHANOL: 50.6% WT/WTINSOL IN WATER.SOL IN ANILINESOL IN ETHERSolubility in water: very poor0.045g/lINSOLUBLE
Flammpunkt176 °F (USCG, 1999)82 °C171 °F (77 °C) (OPEN CUP)180 °F (82 °C) (CLOSED CUP)160 °F (71 °C) (CLOSED CUP)176 °C (Closed cup)190 °F (Open cup)77 °C o.c.
Siedepunkt406 °F at 760 mmHg (USCG, 1999)207.6 °C @ 760 MM HG207.2 °C @760 [mm Hg]207 °C (lit.)
DecompositionUNDER ... PYROLYSIS AT 700 °C, TETRALIN ... YIELDS TARS THAT CONTAIN APPRECIABLE QUANTITIES OF 3,4-BENZOPYRENE.
Schmelzpunkt-35 °C (lit.)
Dampfdichte4.55 (vs air)
Dampfdruck0.18 mm Hg ( 20 °C)
Brechungsindexn20/D 1.541(lit.)
LagerbedingungenStore below +30°C.
AggregatzustandFluid
FarbeColorless
Geruchpungent menthol odor
Geruchsschwelle0.0093ppm
Explosionsgrenze0.8%, 100°F
Spezifische WärmekapazitätCp(liquid): 1.65 J/(g·K), at 25℃
Merck14,9221
BRN1446407
Henry-Konstante6.4×10-3 mol/(m3Pa) at 25℃, Plyasunov and Shock (2000)
Dielektrizitätskonstante2.77
StabilitätStable. Combustible. Incompatible with strong oxidizing agents.
InChI1S/C10H12/c1-2-6-10-8-4-3-7-9(10)5-1/h1-2,5-6H,3-4,7-8H2
InChIKeyCXWXQJXEFPUFDZ-UHFFFAOYSA-N
SMILESC1CCc2ccccc2C1
LogP (Verteilungskoeffizient)3.78 at 23℃
CAS Datenbank119-64-2(CAS DataBase Reference)
NIST chemische InformationenTetralin(119-64-2)
EPA chemische Informationen1,2,3,4-Tetrahydronaphthalene (119-64-2)

Sicherheit & Vorschriften

GHS-EinstufungWarningH315: Causes skin irritation [Warning Skin corrosion/irritation]P264, P264+P265, P273, P280, P302+P352, P305+P351+P338, P321, P332+P317, P337+P317, P362+P364, P391, and P501 (click each P-code to see the statement)This chemical does not meet GHS hazard criteria for 1.5% (11 of 729) of reports.DangerH304 (20.3%): May be fatal if swallowed and enters airways [Danger Aspiration hazard]
Regulatorische InformationenChemical: Naphthalene, 1,2,3,4-tetrahydro-Naphthalene, 1,2,3,4-tetrahydro- is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of Naphthalene, 1,2,3,4-tetrahydro- 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: 11-04-2022 https://echa.europa.eu/registration-dossier/-/registered-dossier/210761,2,3,4-Tetrahydronaphthalene: Does not have an individual approval but may be used under an appropriate group standard
DOT-KennzeichnungCombustible Liquid
BrandgefahrenExcerpt from ERG Guide 128 [Flammable Liquids (Water-Immiscible)]:Combustible. Gives off irritating or toxic fumes (or gases) in a fire. Above 77 °C explosive vapour/air mixtures may be formed.
BrandpotenzialMODERATE, WHEN EXPOSED TO HEAT OR FLAMECAN REACT WITH OXIDIZING MATERIALS. SPONTANEOUS HEATING: NO.
GesundheitsgefahrenLiquid may cause nervous disturbance, green coloration of urine, and skin and eye irritation (USCG, 1999)
GefahrenübersichtListed in table of Methemoglobinemia-inducing agents: industrial, environmental, and pharmaceutical[Sullivan, p. 729]Tetralin is a skin and mucous membrane irritant. When used in poorly ventilated areas, tetralin may cause central nervous system depression. Ingestion of tetralin has caused green urine and laboratory evidence of liver and kidney injury. [HSDB] A skin, eye, and respiratory tract irritantInhalation of high concentrations may cause CNS effectsMay cause kidney injury[ICSC]
Reaktive GruppeHydrocarbons, Aromatic
EG-EinstufungSymbol: Xi, NR: 19-36/38-51/53S: (2)-26-28-61
Special ReportsBEAUMONT D, WAIGH RDTHE BETA-ADRENOMIMETIC ACTIVITY OF TETRAHYDROISOQUINOLINESAND TETRAHYDRONAPHTHALENES. PROG MED CHEM 18: 45-86 (1981). A REVIEW WITH 155 REFERENCES ON THE BETA-ADRENOMIMETIC ACTIVITY OF 1,2,3,4-TETRAHYDROISOQUINOLINE AND 1,2,3,4-TETRAHYDRONAPHTHALENE DERIVATIVES.Nelson NA et alSolvent Nephrotoxicity in Humans and Experimental Animals. Am J Nephrol 10 (1): 10-20 (1990). Evidence from human case reports, epidemiologic studies and animal experiments have suggested that exposure to organic solvents is associated with a wide spectrum of renal disorders, including tubular necrosis, interstitial disease, glomerulonephritis and neoplasia. This review summarizes what is known about solvent induced renal damage in humans and experimental animals, with emphasis on hypothesized mechanisms by which this broad range of disorders may occur.
Reactivity AlertsPeroxidizable Compound
Reactivity ProfileTETRAHYDRONAPHTHALENE may react vigorously with strong oxidizing agents. May react exothermically with reducing agents to release hydrogen gas. Oxidizes readily in air to form unstable peroxides that may explode spontaneously [Bretherick 1979 p.151-154].
Chemical DangersThe substance can form explosive peroxides. Decomposes on heating. This produces irritating fumes. Reacts vigorously with oxidants.
BrandbekämpfungExcerpt from ERG Guide 128 [Flammable Liquids (Water-Immiscible)]:Use water spray, powder, foam, carbon dioxide. In case of fire: keep drums, etc., cool by spraying with water.
Erste-Hilfe-MaßnahmenFresh air, rest. Refer for medical attention.Rinse skin with plenty of water or shower. Remove contaminated clothes.First rinse with plenty of water for several minutes (remove contact lenses if easily possible), then refer for medical attention.Do NOT induce vomiting. Give one or two glasses of water to drink. Refer for medical attention .
Erste HilfeINGESTION: induce vomitingcall a doctormedical treatment should be aimed at conservation of liver and kidney function.
Sichere LagerungSeparated from strong oxidants. Keep in a well-ventilated room. Well closed.
Expositionsschutz und Persönliche Schutzausrüstung2.0 [ppm]
BrandbekämpfungsverfahrenWATER MAY BE INEFFECTIVE ON FIRE. COOL EXPOSED CONTAINERS WITH WATER.
LagerbedingungenIN GENERAL MATERIALS ... TOXIC AS STORED OR WHICH CAN DECOMP INTO TOXIC COMPONENTS ... SHOULD BE STORED IN COOL ... VENTILATED PLACE, OUT OF ... SUN, AWAY FROM ... FIRE HAZARD ... BE PERIODICALLY INSPECTED & MONITORED. INCOMPATIBLE MATERIALS SHOULD BE ISOLATED.
Freisetung ohne BrandExcerpt from ERG Guide 128 [Flammable Liquids (Water-Immiscible)]:
Verschüttetes entsorgenPersonal protection: chemical protection suit. Do NOT let this chemical enter the environment. Ventilation. Collect leaking and spilled liquid in covered containers as far as possible. Absorb remaining liquid in sand or inert absorbent. Then store and dispose of according to local regulations.
Preventive MeasuresSRP: The scientific literature for the use of contact lenses in industry is conflicting. The benefit or detrimental effects of wearing contact lenses depend not only upon the substance, but also on factors including the form of the substance, characteristics and duration of the exposure, the uses of other eye protection equipment, and the hygiene of the lenses. However, there may be individual substances whose irritating or corrosive properties are such that the wearing of contact lenses would be harmful to the eye. In those specific cases, contact lenses should not be worn. In any event, the usual eye protection equipment should be worn even when contact lenses are in place.
Isolation and EvacuationExcerpt from ERG Guide 128 [Flammable Liquids (Water-Immiscible)]:
Eye PreventionWear safety spectacles.
UmweltverhaltenTERRESTRIAL FATE: If released to soil, adsorption is expected to take place. However, it has been detected in groundwater beneath a municipal landfill(4) and the annual loadings of tetralin in runoff from land in the Canadian Ontario and Great Lakes water basins are estimated to be 1,053 and 2,270 kg/yr, respectively(5). Based on biodegradation half-lives of 4-13 days in aquatic systems(1-3), biodegradation in soil will be important(SRC).AQUATIC FATE: Based on the estimated Henry's Law constant of 1.7X10-3 atm-cu m/mol at 25 °C(2), volatilization half-lives from a model river (1 m deep flowing 1 m/sec and wind velocity of 3 m/sec) and lake (1 m deep) can be estimated to be 4 hours and 5 days, respectively(1,SRC). An estimated Koc value of 1,800(3) suggests a high adsorption potentialfurthermore, tetralin was detected in suspended solids from St. Louis Bay(4). Screening and grab sample tests indicate a biodegradation half-life of 4-13 days in seawater, groundwater, and river water(5-7). Bioconcentration in fish may be important in organisms that cannot metabolize tetralin(8).ATMOSPHERIC FATE: Based on the experimental vapor pressure of 0.368 mm Hg at 25 °C(1), tetralin is expected to exist almost entirely in the vapor phase in the ambient atmosphere(2). Vapor phase tetralin will degrade rapidly in the ambient atmosphere by reaction with photochemically produced hydroxyl radicals with a half-life of about 11 hours(3,SRC). Vapor phase tetralin will also degrade in the ambient atmosphere at night-time by reaction with nitrate radicals with a half-life of about 3.6 days(4-5,SRC).
Unerwünschte WirkungenNeurotoxin - Acute solvent syndrome
Signs and SymptomsCough. Dizziness. Headache. Nausea. Vomiting. Weakness.Redness. Pain.Pain. Redness. Blurred vision.Abdominal pain. See Inhalation.
Ongoing Test StatusThe following link will take the user to the National Toxicology Program (NTP) Test Agent Search Results page, which tabulates all of the "Standard Toxicology & Carcinogenesis Studies", "Developmental Studies", and "Genetic Toxicity Studies" performed with this chemical. Clicking on the "Testing Status" link will take the user to the status (i.e., in review, in progress, in preparation, on test, completed, etc.) and results of all the studies that the NTP has done on this chemical. [http://ntp-apps.niehs.nih.gov/ntp_tox/index.cfm?fuseaction=ntpsearch.searchresults&searchterm=119-64-2]
Effluent ConcentrationsTetralin was identified at a concn range of 13.3-154.3 ng/L in paper-mill effluents being discharged into the Rainy River(1). Tetralin was qualitatively identified in advanced waste treatment water from Lake Tahoe, CA in October of 1974(2). Tetralin was detected at a concn range of 2-58 ug/mL in 5 incinerator effluent extracts(3). Tetralin was detected 1 km from a Volvo assembly plant in Goteborg, Sweden at a concn of 4.6 ug/cu-m on January 14, 1981regional Goteburg air contains less than 0.01 ug/cu-m tetralin(4). Also, 30 ug/cu-m tetralin was detected in air nearby a Saab assembly plant in Sweden on January 19, 1981(4). These data suggest tetralin is released from automobile assembly plants in emissions from solvents used during painting processes(4). Tetralin emission rates from well-tuned radiant and maltuned convective kerosene space heaters ranged from 100-240 ng/kJ(5).Based upon monitoring data of runoff from land, approximately 1,053 and 2,271 kg tetralin/yr are input to the Canadian Lake Ontario and Canadian Great Lakes water basins, respectively(1). Tetralin was detected at a concn of 11 ng/g in wastewater from the petroleum refining industry after dissolved air flotation(2).
ICSC Environmental DataThe substance is toxic to aquatic organisms. Bioaccumulation of this chemical may occur in fish. It is strongly advised not to let the chemical enter into the environment.
Soil Adsorption/MobilityA Koc for tetralin of about 1,800 can be estimated using a structure activity relationship(1). Based on a suggested classification scheme(2), this Koc value suggests that tetralin has low mobility in soil.
Atmospheric ConcentrationsINDOOR AIR: Tetralin was detected at concns of 10 and 20 ug/cu-m in 2 of 6 indoor air samples taken mostly from homes in northern Italy(1).
Human Toxicity Excerpts... IN HIGH CONCENTRATIONS, /SRP: CNS DEPRESSANT/ ... .... VAPORS ARE KNOWN TO PRODUCE HEADACHE, NAUSEA, VOMITING, AND IRRITATION OF CONJUNCTIVA AND OF RESPIRATORY TRACT MUCOSA. HIGH CONCENTRATIONS PRODUCE /CNS DEPRESSION/.Dermal exposure to tetralin has caused eczematous dermatitis, but only rarely, and exposure to tetralin fumes in poorly ventilated places has produced /CNS depressant/ effects including marked restless, eye irritation, headache, malaise, asthenia, nausea, and vomiting.A hallmark for tetralin exposure in man is the production of green colored urine. ... Green urine /was reported/ from a man who had ingested 5.7 g of a pigment called di-tetralin. ... Two cases of "tetralin urine" /were reported/ in painters who used tetralin-containing varnishes in a poorly ventilated areathese workers also showed intense irritation of the mucous membranes, profuse lacrimation , headache, and stupor.For more Human Toxicity Excerpts (Complete) data for TETRALIN (12 total), please visit the HSDB record page.
Fish/Seafood ConcentrationsTetralin was detected in small mouth bass (Micropterus dolomieui) at a concn of 75.3 ng/g and yellow perch (Perca flavescens) at concns of 73.2 and 34.5 ng/g from the Rainy River which forms an international boundary between the U.S. and Canada(1).
Artificial Pollution SourcesTetralin is released to the environment in emissions from automobile and diesel engines(1), incinerators(2), kerosene space heaters(3), and from automobile assembly plants during painting processes(4). Tetralin is released in effluents from paper-mills(5), petroleum refineries(6), and in advanced waste treatment effluents(7). Tetralin may also be released to surface waters via runoff from land(8).
Environmental BiodegradationDEGRADATION IN SEA WATER BY OIL OXIDIZING MICROORGANISMS: 31% BREAKDOWN AFTER 21 DAYS AT 22 °C IN STOPPERED BOTTLES CONTAINING A 1000 PPM MIXTURES OF ALKANES, CYCLOALKANES, AND AROMATICS.One screening test using sewage seed suggests that tetralin (initial concn of 3-10 ppm) biodegrades slowly in synthetic seawater3, 3, 2, and 3 percent theoretical BOD in 5, 10, 15, and 20 days, respectively(1). However, 0.0124 ppm tetralin was not detected after 10 days of incubation in artificial seawater at 25 °C indicating that tetralin is moderately oxidized(2). An initial concn of 0.0112 ppm tetralin was observed to degrade 100% in 8 days in a groundwater grab sample at 10 °C and pH 8(3). Tetralin (20.1 ppm initial concn) exhibited 18, 40, 58, 65, 70, and 75 percent theoretical CO2 production after 5, 10, 15, 20, 25, and 35 days, respectively, in water from the Ohio River at 22-25 °C and pH 7.2the half-life in this study was 13 days and, after redosing, a half-life of 9 days was observed under the same conditions(4).
Wassergefährdungsklasse (WGK)2
TSCA-Inventar-StatusTSCA listed
UN-TransportnummerUN 3082 9/PG 3
Zollcode2902 90 00
RTECS-Nr.QK3850000
R-Sätze (R)19-36/38-51/53-65-40
ToxizitätLD50 orally in rats: 2.86 g/kg (Smyth)
GefahrensymboleXi,N,Xn
Sicherheitshinweise (S)26-28-61-28A-62-36/37
Gefahrenklasse9Aquatic Chronic 2Asp. Tox. 1Carc. 2Eye Irrit. 2Skin Irrit. 2
VerpackungsgruppeIII
Lagerklasse10 - Combustible liquids
Gefahrstoffdaten119-64-2(Hazardous Substances Data)
Selbstentzündungstemperatur723 °F

Anwendungen & Verwendung

Verwenden

1,2,3,4-Tetrahydronaphthalene, is used as an intermediate for organic synthesis, solvent. It is used as a solvent.It is also used for the laboratory synthesis of dry HBr gas.