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

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

CAS: 104-29-0 | C9H11ClO3 | 202.634 g/mol
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Catalog number A17386.36
also known as A17386-36
Price (EUR)
585,00
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Quantity:
500 g
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Price (EUR)
585,00
Each
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Chemical Identifiers
CAS104-29-0
IUPAC Name3-(4-chlorophenoxy)propane-1,2-diol
Molecular FormulaC9H11ClO3
InChI KeyMXOAEAUPQDYUQM-UHFFFAOYNA-N
SMILESOCC(O)COC1=CC=C(Cl)C=C1
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SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)White
Melting Point76.5-82.5?C
FormCrystals or powder or crystalline powder
Identification (FTIR)Conforms
Assay (GC)≥98.5%
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.