Name | 1,2,4-Trimethoxybenzene |
Synonyms | cerium(3+) phosphate 1,2,4-Trimethoxybenzol 1,2,4-trimethoxy-benzen 1,2,4-Trimethoxybenzene 1,2,4-TRIMETHOXYBENZENE 1.2.4-Trimethoxy benzone Benzene, 1,2,4-trimethoxy- 1,2,4-Benzenetriol trimethyl ether Hydroxyhydroquinone trimethyl ether HYDROXYHYDROQUINONE TRIMETHYL ETHER |
CAS | 135-77-3 |
EINECS | 205-219-7 |
InChI | InChI=1/C9H12O3/c1-10-7-4-5-8(11-2)9(6-7)12-3/h4-6H,1-3H3 |
Molecular Formula | C9H12O3 |
Molar Mass | 168.19 |
Density | 1.126g/mLat 25°C(lit.) |
Melting Point | 19 - 21℃ |
Boling Point | 247°C(lit.) |
Flash Point | >230°F |
Water Solubility | Not miscible in water. |
Solubility | Chloroform, Ethyl Acetate |
Vapor Presure | 0.0413mmHg at 25°C |
Appearance | Transparent liquid |
Color | Clear Colourless |
Merck | 14,1073 |
BRN | 2047579 |
Storage Condition | Sealed in dry,Room Temperature |
Refractive Index | n20/D 1.533(lit.) |
MDL | MFCD00008360 |
Physical and Chemical Properties | Density 1.128 boiling point 247°C refractive index 1.532-1.534 |
Use | Used as a pharmaceutical Intermediate |
Hazard Symbols | Xi - Irritant |
Safety Description | S23 - Do not breathe vapour. S24/25 - Avoid contact with skin and eyes. |
WGK Germany | 3 |
RTECS | DC2770000 |
TSCA | Yes |
HS Code | 29093090 |
Hazard Note | Irritant |
Reference Show more | 1. [IF=5.279] Xueli Pang et al."Comparison of Potent Odorants in Raw and Ripened Pu-Erh Tea Infusions Based on Odor Activity Value Calculation and Multivariate Analysis: Understanding the Role of Pile Fermentation."J Agr Food Chem. 2019;67(47):13139–13149 |
NIST chemical information | Information provided by: webbook.nist.gov (external link) |
EPA chemical information | Information provided by: ofmpub.epa.gov (external link) |
use | intermediate. Used as a pharmaceutical intermediate |
Production method | Vanillin is oxidized with hydrogen peroxide, then hydrolyzed, and methylated with dimethyl sulfate to prepare; or hydroquinone is oxidized with sodium dichromate and sulfuric acid to produce p-benzodiquinone, which is acetylated with acetic anhydride to obtain 1,2, 4-phlorotriacetate, and the latter is methylated with dimethyl sulfate to prepare the product. |