4-Hydroxy-2-methylbenzaldehyde
4-Hydroxy-2-methylbenzaldehyde Basic information
- Product Name:
- 4-Hydroxy-2-methylbenzaldehyde
- Synonyms:
-
- 4-HYDROXY-2-METHYLBENZALDEHYDE
- Benzaldehyde, 4-hydroxy-2-methyl-
- 4-Hydroxy-2-methylbenzenecarbaldehyde
- 4-Hydroxy-o-tolualdehyde. m-Cresol-4-aldehyde. 4,2
- 5'-Ethylpropiophenone
- CAS:
- 41438-18-0
- MF:
- C8H8O2
- MW:
- 136.15
- Product Categories:
-
- Benzaldehyde
- Aromatic Aldehydes & Derivatives (substituted)
- Mol File:
- 41438-18-0.mol
4-Hydroxy-2-methylbenzaldehyde Chemical Properties
- Melting point:
- 104-107°C
- Boiling point:
- 205-207 °C(Press: 18 Torr)
- Density
- 1.175±0.06 g/cm3(Predicted)
- storage temp.
- under inert gas (nitrogen or Argon) at 2-8°C
- form
- solid
- pka
- 7.89±0.18(Predicted)
- Appearance
- Light yellow to brown Solid
- InChI
- 1S/C8H8O2/c1-6-4-8(10)3-2-7(6)5-9/h2-5,10H,1H3
- InChIKey
- JDWWIEFMFPWBST-UHFFFAOYSA-N
- SMILES
- Cc1cc(O)ccc1C=O
- CAS DataBase Reference
- 41438-18-0(CAS DataBase Reference)
Safety Information
- Hazard Codes
- Xn,Xi
- Risk Statements
- 36/37/38-52-41-37/38
- Safety Statements
- 26-36/37/39-39
- WGK Germany
- WGK 3
- HS Code
- 2914500090
- Storage Class
- 11 - Combustible Solids
- Hazard Classifications
- Eye Dam. 1
4-Hydroxy-2-methylbenzaldehyde Usage And Synthesis
Uses
2-Methyl-4-hydroxybenzaldehyde can be used in organic synthesis and can also be used as a reference standard for the analysis and detection of Compound Snow Lotus Capsules.
Chemical Properties
2-Methyl-4-hydroxybenzaldehyde appears as a white to pale yellow crystalline powder, slightly soluble in water and soluble in oil.
Synthesis
Magnesium powder (14.4 g, 0.6 mol) was put into a four-necked reaction bottle containing 200 ml of methanol, electric stirring was turned on, a large number of bubbles were produced in the bottle, and the temperature was increased to 61??C. After 2 h, the solution turned into a milky white suspension. P-toluene (108g, 1.0 mol) was added to the reaction bottle, and after 50 min, methanol started to be evaporated, and when the reaction solution became thick, 200 ml of toluene was made up. Increase the temperature, when the internal temperature reached 95 ??, add paraformaldehyde (90g, 3.0mol) in batches, the device was changed to a distillation device, evaporation of low-boiling substances, after 30min almost no fraction evaporated, withdraw the distillation device, continue to react for 2.5h, tracked with a TLC dot plate, the reaction of p-methylphenol was complete. Stop heating, wait for the internal temperature to drop to 65??C, adjust ph=1 with 18.5% hydrochloric acid. leave to stand and separate the liquid, the organic layer was extracted with 70ml toluene for 2 times, the organic layer was combined, the organic layer was washed with water for 3 times until the ph was close to 7. 2-methyl-4-hydroxybenzaldehyde was obtained.
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4-Hydroxy-2-methylbenzaldehyde(41438-18-0)Related Product Information
- 4-Hydroxybenzaldehyde
- 3-(Trifluoromethyl)benzaldehyde
- 2-(Trifluoromethyl)benzaldehyde
- CHLOROPHOSPHONAZO III
- 3-Hydroxybenzaldehyde
- 2-Methylbenzaldehyde
- Salicylaldehyde
- p-Tolualdehyde
- Emodin
- PURPURIN
- 2,6-DIHYDROXYANTHRAQUINONE
- 2,3-DIMETHYLANISALDEHYDE
- 4'-HYDROXY-2'-METHYLACETOPHENONE
- 4-HYDROXY-3-METHYLBENZALDEHYDE
- Alizarin
- 5-METHOXY-1-INDANONE-3-ACETIC ACID
- 2,5-DIMETHYL-P-ANISALDEHYDE
- Ethyl 2,4-dihydroxy-6-methylbenzoate