(R)-(+)-Propylene oxide, 99%
(R)-(+)-Propylene oxide, 99%
(R)-(+)-Propylene oxide, 99%
Thermo Scientific Chemicals

(R)-(+)-Propylene oxide, 99%

CAS: 15448-47-2 | C3H6O | 58.08 g/mol
数量:
5 g
25 g
100 g
製品番号(カタログ番号) B21884.22
または、製品番号B21884-22
価格(JPY)
-
数量:
100 g
一括またはカスタム形式をリクエストする
化学物質識別子
CAS15448-47-2
IUPAC Name(2R)-2-methyloxirane
Molecular FormulaC3H6O
InChI KeyGOOHAUXETOMSMM-GSVOUGTGSA-N
SMILESC[C@@H]1CO1
さらに表示
Optical Rotation13.0 ± 2.0? (neat)
Refractive Index1.3655-1.3685 @ 20?C
Appearance (Color)Clear colorless
FormLiquid
Assay (GC)≥98.5%
さらに表示
(R)-(+)-Propylene oxide is widely utilized in the manufacture of polyether polyols and propylene glycol, which is used to make the polyurethane plastics. It finds application as a fumigant for the sterilization of packaged foods and plastic medical instruments. Combine with ethanol, it used to make biological samples for electron microscopy. It also used in model aircraft and surface vehicles as a glow fuel.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
(R)-(+)-Propylene oxide is widely utilized in the manufacture of polyether polyols and propylene glycol, which is used to make the polyurethane plastics. It finds application as a fumigant for the sterilization of packaged foods and plastic medical instruments. Combine with ethanol, it used to make biological samples for electron microscopy. It also used in model aircraft and surface vehicles as a glow fuel.

Solubility
Miscible with water and many organic solvents.

Notes
Highly flammable. Keep away from sources of ignition. The substance may polymerize under the influence of bases, acids and metal chlorides.
RUO – Research Use Only

General References:

  1. Paddock, R. L.; Adhikari, D.; Lord, R. L.; Baik, M.; Nguyen, S. T. [(Salcen)CrIII + Lewis base]-catalyzed synthesis of N-aryl-substituted oxazolidinones from epoxides and aryl isocyanates. Chem. Commun. 2014, 50 (96), 15187-15190.
  2. Horvath, J. D.; Gellman, A. J. Enantiospecific Desorption of R- and S-Propylene Oxide from a Chiral Cu(643) Surface. J. Am. Chem. Soc. 2001, 123 (32), 7953-7954.