Name | 2,5-dimethylpyrrole |
Synonyms | BMPy Dimethylpyrrole 2,5-dimethyl-pyrrol 2,5-dimethylpyrrole 2,5-bimethylpyrrole pyrrole,2,5-dimethyl- Pyrrole, 2,5-dimethyl- 2,5-1H-dimethylpyrrole 2,5-dimethyl-1h-pyrrol 2,5-dimethyl-1h-pyrrole 2,5-Dimethyl Pyrrole (625-84-3) |
CAS | 625-84-3 |
EINECS | 210-913-8 |
InChI | InChI=1/C6H9N/c1-5-3-4-6(2)7-5/h3-4,7H,1-2H3 |
InChIKey | PAPNRQCYSFBWDI-UHFFFAOYSA-N |
Molecular Formula | C6H9N |
Molar Mass | 95.14 |
Density | 0.935 g/mL at 25 °C (lit.) |
Melting Point | 6.5°C |
Boling Point | 165 °C/740 mmHg (lit.) |
Flash Point | 130°F |
Water Solubility | Insoluble in water |
Vapor Presure | 44-490Pa at 20-50℃ |
Appearance | Crystalline Powder and/or Chunks |
Specific Gravity | 0.935 |
Color | Yellow to orange-yellow |
pKa | 18.46±0.50(Predicted) |
Storage Condition | Keep in dark place,Sealed in dry,Room Temperature |
Refractive Index | n20/D 1.505(lit.) |
MDL | MFCD00005223 |
Physical and Chemical Properties | Colorless to yellowish oily liquid. There was strong irritation odor. Boiling point 165 °c. Miscible in ethanol and ether, very difficult to dissolve in water. Red resin can be formed in the air. |
Use | Intermediates in organic synthesis. |
Risk Codes | R10 - Flammable R23/24/25 - Toxic by inhalation, in contact with skin and if swallowed. R36/37/38 - Irritating to eyes, respiratory system and skin. |
Safety Description | S16 - Keep away from sources of ignition. 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. S45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.) |
UN IDs | UN 1992 3/PG 3 |
WGK Germany | 3 |
RTECS | UX9465930 |
HS Code | 29339900 |
Hazard Class | 3.2 |
Packing Group | III |
NIST chemical information | information provided by: webbook.nist.gov (external link) |
content analysis | analysis was performed on a polar column in gas chromatography (GT-10-4). |
Use | flavor. intermediates in organic synthesis. The product is used for the polymerization of ethylene to produce hexene-1 |
production method | heating 2, 5-hexanedione and ammonium carbonate together until the foaming phenomenon stops, it takes about 1-1.5H, the mixture was refluxed slowly for another half hour at 115 ° C., cooled, and the upper layer, 2, 5-dimethylpyrrole, was separated. The lower layer of the above reactant is extracted with chloroform, and a part of the product can be recovered. The crude product was distilled under reduced pressure, and fractions of 51-53 °c (1.07kPa) or 78-80 °c (3.33kPa) were collected to obtain the finished product. The yield was 81-86%. obtained by sealing an alcohol solution of acetone-based acetone and ammonia in a tube and heating. Derived from the interaction of magnesium pyrrole bromide and methyl iodide. |