| Identification | More | [Name]
3-Methoxyphenol | [CAS]
150-19-6 | [Synonyms]
1-HYDROXY-3-METHOXYBENZENE
3-HYDROXYANISOL
3-HYDROXYANISOLE
3-METHOXYPHENOL
M-HYDROXYANISOLE
M-METHOXYPHENOL
RESORCINOL MONOMETHYL ETHER
3-methoxy-pheno
m-Guaiacol
m-methoxy-pheno
Phenol, 3-methoxy-
Phenol, m-methoxy-
Resorcinol methyl ether
resorcinolmethylether
3-Hydroxy phenyl methyl ether
3-Methoxyphenol,3-Hydroxyanisol
RESORCINOLMETA-MONOMETHYLETHER
META-METHOXYPHENOL
3-Hydroxyanisol, Resorcinol monomethyl ether
3-Methxoyphenol | [EINECS(EC#)]
205-754-6 | [Molecular Formula]
C7H8O2 | [MDL Number]
MFCD00002267 | [Molecular Weight]
124.14 | [MOL File]
150-19-6.mol |
| Chemical Properties | Back Directory | [Appearance]
Clear pink red liquid | [Melting point ]
-17 °C
| [Boiling point ]
113-115 °C/5 mmHg (lit.) | [density ]
1.131 g/mL at 25 °C(lit.)
| [refractive index ]
n20/D 1.552(lit.)
| [Fp ]
>230 °F
| [storage temp. ]
Store in dark! | [solubility ]
Chloroform (Slightly), Ethyl Acetate (Slightly) | [form ]
Liquid | [pka]
9.65(at 25℃) | [color ]
Clear pink-reddish to brown | [Odor]
at 1.00?%?in?dipropylene glycol. phenolic | [Water Solubility ]
slightly soluble | [BRN ]
1209898 | [Cosmetics Ingredients Functions]
SKIN CONDITIONING | [InChI]
1S/C7H8O2/c1-9-7-4-2-3-6(8)5-7/h2-5,8H,1H3 | [InChIKey]
ASHGTJPOSUFTGB-UHFFFAOYSA-N | [SMILES]
COc1cccc(O)c1 | [LogP]
1.340 | [CAS DataBase Reference]
150-19-6(CAS DataBase Reference) | [NIST Chemistry Reference]
3-Methoxyphenol(150-19-6) | [EPA Substance Registry System]
Phenol, 3-methoxy- (150-19-6) |
| Safety Data | Back Directory | [Symbol(GHS) ]
 
GHS05,GHS06 | [Signal word ]
Danger | [Hazard statements ]
H302+H332-H311-H315-H318 | [Precautionary statements ]
P261-P280-P301+P312-P302+P352+P312-P304+P340+P312-P305+P351+P338 | [Hazard Codes ]
Xn | [Risk Statements ]
R20/21/22:Harmful by inhalation, in contact with skin and if swallowed .
R36/38:Irritating to eyes and skin .
R41:Risk of serious damage to eyes.
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection . | [RIDADR ]
UN 2810 6.1/PG 3
| [WGK Germany ]
3
| [RTECS ]
SL7524000
| [TSCA ]
Yes | [HazardClass ]
6.1 | [PackingGroup ]
III | [HS Code ]
29095090 | [Storage Class]
6.1C - Combustible, acute toxic Cat.3
toxic compounds or compounds which causing chronic effects | [Hazard Classifications]
Acute Tox. 3 Dermal
Acute Tox. 4 Inhalation
Acute Tox. 4 Oral
Eye Dam. 1
Skin Irrit. 2 | [Safety Profile]
Poison by ingestion and intraperitoneal routes. Moderately toxic by skin contact. Human systemic effects by inhalation: muscle weakness, headache, and irritabdtty. Human female reproductive effects by inhalation: menstrual cycle changes and dsorders. A severe eye irritant. When heated to decomposition it emits acrid smoke and irritating fumes. See also ETHERS. | [Toxicity]
human,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. |
| Hazard Information | Back Directory | [Chemical Properties]
Clear pink red liquid | [Uses]
3-Methoxyphenol may be used as an analytical standard for the determination of the analyte in wine, coffee beans, wood samples, and mainstream smoke by gas chromatography (GC) based techniques. | [Uses]
A phenol derivative, 3-Methoxyphenol can be used as catalysts and as building blocks in synthesis of organic compounds such as antioxidants.
| [Definition]
ChEBI: A member of the class of phenols that is phenol having a methoxy-substituent at the 3-position. | [Preparation]
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) | [General Description]
3-Methoxyphenol is a phenolic aroma compound typically present in food and beverage products. |
|
| Company Name: |
J & K SCIENTIFIC LTD.
|
| Telephone: |
18210857532 18210857532 |
| Website: |
https://www.jkchemical.com |
| Company Name: |
Alfa Aesar
|
| Telephone: |
400-6106006 |
| Website: |
http://chemicals.thermofisher.cn |
|