3-Ethoxy-4-hydroxybenzaldehyde, 98%, Thermo Scientific Chemicals
3-Ethoxy-4-hydroxybenzaldehyde, 98%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

3-Ethoxy-4-hydroxybenzaldehyde, 98%, Thermo Scientific Chemicals

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25 g
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500 g
Catalog number A19478.14
also known as A19478-14
Price (USD)/ Each
20.65
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Quantity:
25 g
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Price (USD)/ Each
20.65
Online exclusive
22.50 
Save 1.85 (8%)
Add to cart
3-Ethoxy-4-hydroxybenzaldehyde, 98%, Thermo Scientific Chemicals
Catalog numberA19478.14
Price (USD)/ Each
20.65
Online exclusive
22.50 
Save 1.85 (8%)
-
Add to cart
Chemical Identifiers
CAS121-32-4
IUPAC Name3-ethoxy-4-hydroxybenzaldehyde
Molecular FormulaC9H10O3
InChI KeyCBOQJANXLMLOSS-UHFFFAOYSA-N
SMILESCCOC1=CC(C=O)=CC=C1O
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SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)White
Melting Point (clear melt)74.0-80.0?C
FormCrystals or powder or crystalline powder or flakes
Identification (FTIR)Conforms
Assay (GC)≥97.5%
It plays an important role as an antioxidant and is also used as a flavoring agent, in perfumes, and in organic synthesis. It holds anti-angiogenic, anti-inflammatory and antinociceptive properties.

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 plays an important role as an antioxidant and is also used as a flavoring agent, in perfumes, and in organic synthesis. It holds anti-angiogenic, anti-inflammatory and antinociceptive properties.

Solubility
Slightly soluble in water. Soluble in ethanol, ether, benzene.

Notes
Air & light sensitive. Protect from light. Store away from oxidizing agents and air. Keep the container tightly closed and place it in a cool, dry and well ventilated condition.
RUO – Research Use Only

General References:

  1. Tai A.; Sawano T.; Yazama F. Antioxidant properties of ethyl vanillin in vitro and in vivo. Bioscience, biotechnology, and biochemistry.2011,75(12), 2346-2350.
  2. Jung HJ, et al. Assessment of the anti-angiogenic, anti-inflammatory and antinociceptive properties of ethyl vanillin.Arch. Pharmacal Res.2010,33(2), 309-316.