3-(4-Chlorophenoxy)-1,2-propanediol, 99%, Thermo Scientific Chemicals
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3-(4-Chlorophenoxy)-1,2-propanediol, 99%, Thermo Scientific Chemicals
3-(4-Chlorophenoxy)-1,2-propanediol, 99%, Thermo Scientific Chemicals
3-(4-Chlorophenoxy)-1,2-propanediol, 99%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

3-(4-Chlorophenoxy)-1,2-propanediol, 99%, Thermo Scientific Chemicals

CAS: 104-29-0 | C9H11ClO3 | 202.634 g/mol
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Catalog number ALFA17386.36
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Chemical Identifiers
CAS1115-30-6
IUPAC Name1,4-diethyl 2-acetylbutanedioate
Molecular FormulaC10H16O5
InChI KeyDVSDDICSXBCMQJ-UHFFFAOYNA-N
SMILESCCOC(=O)CC(C(C)=O)C(=O)OCC
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SpecificationsSpecification SheetSpecification Sheet
Assay (GC)≥97.0%
Refractive Index1.4325-1.4375 @ 20?C
FormLiquid
Appearance (Color)Clear colorless to pale yellow
It inhibits IgE-mediated histamine release. 3-(4-Chlorophenoxy)-1,2-propanediol is also used as an antimycotic agent. It is a centrally acting muscle relaxant.

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
It inhibits IgE-mediated histamine release. 3-(4-Chlorophenoxy)-1,2-propanediol is also used as an antimycotic agent. It is a centrally acting muscle relaxant.

Solubility
Slightly soluble in water.

Notes
Store at 78-82°C. Keep away from strong oxidizing agents.
RUO – Research Use Only

General References:

  1. James P. Collman.; James A. Belmont.; John I. Brauman. A silica-supported rhodium hydroformylation catalyst: evidence for dinuclear elimination. J. Am. Chem. Soc. 1983, 105 (25), 7288-7294.
  2. Jing Quan, Qi Wu.; Xian-Fu Lin. Synthesis of polymeric prodrugs of chlorphenesin with saccharide branches by chemo-enzymatic regioselective strategy. Polymer. 2007, 48 (9),2595-2604.