(R)-()-Propylene oxide

99%

Reagent Code: #229889
label
Alias (R)-(+)-propylene oxide
fingerprint
CAS Number 15448-47-2

science Other reagents with same CAS 15448-47-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 58.08 g/mol
Formula C₃H₆O
badge Registry Numbers
MDL Number MFCD00066211
thermostat Physical Properties
Boiling Point 33-34 °C(lit.)
inventory_2 Storage & Handling
Density 0.829 g/mL at 20 °C(lit.)
Storage 2~8°C

description Product Description

Used primarily as a chiral building block in the synthesis of fine chemicals and pharmaceuticals. Its reactivity as an epoxide allows ring-opening reactions with nucleophiles, enabling the production of enantiomerically pure intermediates. Commonly employed in the manufacture of specialty surfactants, lubricants, and functional fluids where optical activity influences performance. Also utilized in asymmetric synthesis for drugs requiring specific stereochemistry, contributing to the development of active pharmaceutical ingredients with improved efficacy and reduced side effects.

Available Sizes & Pricing

Size Availability Unit Price Quantity
5ml
10-20 days ฿590.00
25ml
10-20 days ฿1,970.00
100ml
10-20 days ฿7,050.00
500ml
10-20 days ฿24,570.00
(R)-()-Propylene oxide
No image available

Used primarily as a chiral building block in the synthesis of fine chemicals and pharmaceuticals. Its reactivity as an epoxide allows ring-opening reactions with nucleophiles, enabling the production of enantiomerically pure intermediates. Commonly employed in the manufacture of specialty surfactants, lubricants, and functional fluids where optical activity influences performance. Also utilized in asymmetric synthesis for drugs requiring specific stereochemistry, contributing to the development of active

Used primarily as a chiral building block in the synthesis of fine chemicals and pharmaceuticals. Its reactivity as an epoxide allows ring-opening reactions with nucleophiles, enabling the production of enantiomerically pure intermediates. Commonly employed in the manufacture of specialty surfactants, lubricants, and functional fluids where optical activity influences performance. Also utilized in asymmetric synthesis for drugs requiring specific stereochemistry, contributing to the development of active pharmaceutical ingredients with improved efficacy and reduced side effects.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...