Product Details
Place of Origin: China
Brand Name: Sunshine
Certification: ISO,COA
Model Number: 123-75-1
Payment & Shipping Terms
Minimum Order Quantity: Negotiation
Price: Negotiation
Packaging Details: Plastic bottles, Plastic buckets
Delivery Time: 7-15 days
Payment Terms: T/T, L/C, D/A, Western Union
Supply Ability: TON
CAS NO:: |
123-75-1 |
Appearance:: |
Clear To Yellow Liquid |
Molecular Formula:: |
C4H9N |
Molecular Weight:: |
71.12100 |
EINECS NO:: |
204-648-7 |
MDL NO:: |
MFCD00005249 |
CAS NO:: |
123-75-1 |
Appearance:: |
Clear To Yellow Liquid |
Molecular Formula:: |
C4H9N |
Molecular Weight:: |
71.12100 |
EINECS NO:: |
204-648-7 |
MDL NO:: |
MFCD00005249 |
Product Description:
Product Name: Tetrahydro pyrrole CAS NO: 123-75-1
Synonyms:
PYRROLIDINE,REAGENT;
TETRAHYDROPYRROLE(PYRROLIDINE);
1-AZACYCLOPENTANE;
Chemical & Physical Properties:
Appearance: Clear to yellow liquid
Assay :≥99.0%
Density: 0.866
Boiling Point: 86-88℃
Melting Point: -63℃
Flash Point: 3℃
Refractive Index: 1.4421-1.4441
Stability: Stable; flammable. Incompatible with strong acids, strong oxidizing agents.
Storage Condition: Flammables area
Vapor Density: 2.45 (vs air)
Vapor Pressure: 128 mm Hg ( 39℃)
Water Solubility: Miscible with alcohol, eth-er, chloroform and water
Sensitive: Air sensitive
Safety Information:
RTECS: UX9650000
Hazard Class: 3
Safety Statements: S16-S26-S36/37/39-S45
HS Code: 2933990090
Packing Group: II
WGK Germany: 2
RIDADR: UN 1922
Risk Statements: R11; R20/21/22; R35
Hazard Codes: F; C
Pyrrolidine is a flammable alkaline liquid that undergoes reactions typical of secondary amines. It is used to prepare pesticides and rubber accelerators and as a chemical intermediate (usually the hydrochloride form) in the pharmaceutical industry. There is relatively limited industrial exposure to this material. A heterocyclic compound used as a building block in the synthesis of wide range of pharmaceutical compounds, namely matrix metalloprotein inhibitors (MMPIs) and aminopeptidase N inhibitors (APNIs). Uses of this compound in any major scalehave not been made. It occurs in tobacco andcarrot leaves. It is formed by reduction of pyrrole.
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