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Pyrrolidine

ALDRICH/P73803 - 99%

Synonym: Tetrahydropyrrole; Tetramethyleneimine

CAS Number: 123-75-1
Empirical Formula (Hill Notation): C4H9N
Molecular Weight: 71.12
EC Number: 204-648-7
MDL Number: MFCD00005249
Linear Formula: C4H9N
Product Type: Chemical
Catalog Number PKG Qty. Price Quantity
45-P73803-5ML 5 mL
 $46.70
1/EA		 Add To Favorites
45-P73803-100ML 100 mL
 $54.50
1/EA		 Add To Favorites
45-P73803-500ML 500 mL
 $87.20
1/EA		 Add To Favorites
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: P73803-100ML.
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: P73803-500ML.

 

assay 99%
autoignition temp. 653 °F
density 0.852 g/mL at 25 °C (lit.)
expl. lim. 10.6 %
InChI 1S/C4H9N/c1-2-4-5-3-1/h5H,1-4H2
InChI key RWRDLPDLKQPQOW-UHFFFAOYSA-N
Quality Level 200 
refractive index n20/D 1.443 (lit.)
SMILES string C1CCNC1
vapor density 2.45 (vs air)
vapor pressure 128 mmHg ( 39 °C)
  49 mmHg ( 20 °C)
Application: Pyrrolidine has been used for the synthesis of N-benzoyl pyrrolidine from benzaldehyde via oxidative amination. It may be used as a catalyst for the synthesis of N-sulfinyl aldimines from carbonyl compounds and sulfonamides.
Pyrrolidine can also be used to synthesize:
• Taddol-pyrrolidine phosphoramidite, a ligand for rhodium-catalyzed [2+2+2] cycloaddition of pentenyl isocyanate and 4- ethynylanisole.
• H,4 PyrrolidineQuin-BAM (′PBAM′), a selective catalyst for the aza-Henry addition of nitroalkanes to aryl aldimines.{88]
• 1,2,3,3a,4,9-Hexahydropyrrolo[2,1-b]quinazoline by reacting with o-aminobenzaldehyde.
Packaging: 5, 100, 500 mL in glass bottle
Purity 99%
Density 0.852 g/mL at 25 °C (lit.)
Refractive Index n20/D 1.443 (lit.)
UNSPSC 12352100

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