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HCID 9007Erstellt: 26. Oktober 2026

3-Methoxyphenol

m-Guaiacol · M-METHOXYPHENOL · Phenol, 3-methoxy- · RESORCINOL MONOMETHYL ETHER · NSC 21735 · m-Methoxyphel · meta-guaiacol · 3-Methxoyphenol

https://huagongshe.com/de/chemical/9007

Molekülstruktur von 3-Methoxyphenol

Identifikatoren & physikalische Daten

CAS No.150-19-6
SummenformelC7H8O2
Durchschnittliche Molmasse124,14 g/mol
Monoisotopische Masse124,0524295 g/mol
SMILESCOc1cccc(O)c1
InChIKeyASHGTJPOSUFTGB-UHFFFAOYSA-N
PubChem CID9007
ChEMBLCHEMBL57891
ChEBICHEBI:52678
EC No.205-754-6
DTXSIDDTXSID0022012
Lokaler Name3-Methoxyphenol

Chemische & physikalische Eigenschaften

XLogP1,6
Polarare Oberfläche (TPSA)29,5
H-Brücken-Donoren1
H-Brücken-Akzeptoren2
Frei drehbare Bindungen1
Schwere Atome9
Formalladung0
Komplexität83
StoffklassenOther Classes -> Phenols
SpringerMaterials Properties13C nuclear magnetic resonance spectrum
LogP (Verteilungskoeffizient)1.52
AromastoffeEU Flavoring substances
Siedepunkt471.2 °F113-115 °C/5 mmHg (lit.)
Schmelzpunkt<1.4 °F-17 °C
Dampfdichte1.131
Physical DescriptionAmber liquid with a sweet phenolic odor[OSHA] Clear dark red liquid[Sigma-Aldrich MSDS]
Dichte1.131 g/mL at 25 °C (lit.)
Brechungsindexn20/D 1.552(lit.)
Flammpunkt>230 °F
LagerbedingungenKeep in dark place,Sealed in dry,Room Temperature
LöslichkeitChloroform (Slightly), Ethyl Acetate (Slightly)slightly soluble
AggregatzustandLiquid
pKa (Säurekonstante)9.65(at 25℃)
FarbeClear pink-reddish to brown
Geruchat 1.00%indipropylene glycol. phenolic
BRN1209898
Henry-Konstante1.7×102 mol/(m3Pa) at 25℃, Abraham et al. (1994)
Kosmetik-Inhaltsstoffe FunktionenSKIN CONDITIONING
InChI1S/C7H8O2/c1-9-7-4-2-3-6(8)5-7/h2-5,8H,1H3
InChIKeyASHGTJPOSUFTGB-UHFFFAOYSA-N
SMILESCOc1cccc(O)c1
LogP (Verteilungskoeffizient)1.340
CAS Datenbank150-19-6(CAS DataBase Reference)
NIST chemische Informationen3-Methoxyphenol(150-19-6)
EPA chemische InformationenPhenol, 3-methoxy- (150-19-6)

Sicherheit & Vorschriften

GHS-EinstufungDangerH302 (98.3%): Harmful if swallowed [Warning Acute toxicity, oral]P261, P262, P264, P264+P265, P270, P271, P280, P301+P317, P302+P352, P304+P340, P305+P354+P338, P316, P317, P319, P321, P330, P332+P317, P361+P364, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)Aggregated GHS information provided per 59 reports by companies from 8 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Regulatorische InformationenChemical: Phenol, 3-methoxy-Commission Regulation (EC) No 1565/2000 (Repealed by Com. Implementing Reg. (EU) No 872/2012)3-Methoxyphenol: Does not have an individual approval but may be used under an appropriate group standard
GefahrenübersichtA severe eye irritantCauses flaccid paralysis without anesthesia, tremor, and muscle contraction or spasticity in oral lethal-dose studies of mice and ratsCauses liver and kidney changes and degenerative changes to brain in repeated-dose inhalation studies of guinea pigsHuman inhalation of 0.230 mg/m3 causes muscle weakness, headache, and irritability[RTECS] A skin, eye, and mucous membrane irritantReportedly causes changes or disorders in menstrual cycles[OSHA] An irritant that may cause serious eye injuryHarmful by ingestion and inhalationToxic by skin absorption[Sigma-Aldrich MSDS]
Hazard Classes and CategoriesAcute Tox. 4 (98.3%)
Toxicity DataLC50 (rat) = 11,500 mg/m3/4hr
Wassergefährdungsklasse (WGK)3
TSCA-Inventar-StatusTSCA listed
UN-TransportnummerUN 2810 6.1/PG 3
Zollcode29095090
RTECS-Nr.SL7524000
R-Sätze (R)20/21/22-36/38-41-36/37/38-43-36-22
Toxizitäthuman,TCLo,inhalation,230ug/m3/22W (0.23mg/m3),BEHAVIORAL: IRRITABILITYBEHAVIORAL: MUSCLE WEAKNESSBEHAVIORAL: HEADACHE,Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 37(3), Pg. 108, 1972.
GefahrensymboleXn
Sicherheitshinweise (S)26-36/37/39-46-37/39-24/25
Gefahrenklasse6.1Acute Tox. 3 DermalAcute Tox. 4 InhalationAcute Tox. 4 OralEye Dam. 1Skin Irrit. 2
VerpackungsgruppeIII
Lagerklasse6.1C - Combustible, acute toxic Cat.3toxic compounds or compounds which causing chronic effects

Anwendungen & Verwendung

Verwenden

A phenol derivative, 3-Methoxyphenol can be used as catalysts and as building blocks in synthesis of organic compounds such as antioxidants.

Herstellung & Synthese

synthetische

synthesis of 3-methoxyphenol: The 1 mole of resorcinol is treated rapidly with stirring, in a three-necked flask provided with a reflux condenser, stirrer, internal thermometer, and dropping funnel, with 1.25 mole of 10% sodium hydroxide. With vigorous stirring, 1 mole of dimethyl sulfate is added in such a way that the temperature remains below 40° C (water cooling). To complete the reaction and to destroy unchanged dimethyl sulfate, the mixture is then heated for 30 min on a boiling water bath. After cooling, the organic layer is separated off and the aqueous solution is extracted several times with ether. The combined organic phases are washed with dilute sodium carbonate and then with water, dried with calcium chloride, and fractionated. Unchanged resorcinol can be recovered by acidifying the aqueous reaction solution and the wash water and extracting them with ether. The yield of 3-methoxyphenol is 50%, b.p. 113-115 °C/5 mm; b.p. 144°C/25mm; n20/D 1.552; d=1.131 g/mL at 25 °C. Organicum. Practical Handbook of Organic Chemistry, by Heinz Becker, Werner Berger and Günter Domschke, Addison-Wesley Pub. Co, 206-207, (1973)