Benzaldehyde dimethyl acetal, 99%, Thermo Scientific Chemicals
Benzaldehyde dimethyl acetal, 99%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

Benzaldehyde dimethyl acetal, 99%, Thermo Scientific Chemicals

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Quantity:
500 g
100 g
2500 g
Catalog number A11009.36
also known as A11009-36
Price (USD)/ Each
144.65
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161.00 
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Quantity:
500 g
Request bulk or custom format
Price (USD)/ Each
144.65
Online exclusive
161.00 
Save 16.35 (10%)
Add to cart
Benzaldehyde dimethyl acetal, 99%, Thermo Scientific Chemicals
Catalog numberA11009.36
Price (USD)/ Each
144.65
Online exclusive
161.00 
Save 16.35 (10%)
-
Add to cart
Chemical Identifiers
CAS1125-88-8
IUPAC Name(dimethoxymethyl)benzene
Molecular FormulaC9H12O2
InChI KeyHEVMDQBCAHEHDY-UHFFFAOYSA-N
SMILESCOC(OC)C1=CC=CC=C1
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SpecificationsSpecification SheetSpecification Sheet
Refractive Index1.4910-1.4945 @ 20°C
Appearance (Color)Clear colorless
FormLiquid
Assay (GC)≥98.5%
Identification (FTIR)Conforms
Used in vegetable flavors such as parsley and carrots. For almond, nut, fruit, violet and other nutty and floral fragrances.

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
Used in vegetable flavors such as parsley and carrots. For almond, nut, fruit, violet and other nutty and floral fragrances.

Solubility
Insoluble in water. Soluble in alcohol.

Notes
Keep container tightly closed in a cool, dry and well-ventilated place. Store away from oxidizing agents and acids.
RUO – Research Use Only

General References:

  1. Davis, T.S.; Feil, P.D.; Kubler, D.G.; WellsJr, D.J. Substituent effects on rates and equilibriums for benzaldehyde-benzaldehyde dimethyl acetal interconversion. J. Org. Chem. 1975, 40, (10), 1478-1482.
  2. Paul R. Young.; Roy C. Bogseth.; Edward G. Rietz. Evidence for a solvent-induced change in rate-limiting step in the hydrolysis of benzaldehyde dimethyl acetal. J. Org. Chem. 1980, 102, (20), 6268-6271.
  3. Forms benzylidene derivatives with 1,2 and 1,3-diols, including carbohydrates, by acetal exchange: Carbohydr. Res., 21, 473 (1972); 44, 227 (1975); 137, 282 (1985); Chem. Lett., 335 (1989); J. Chem. Soc., Chem. Commun., 1304 (1992). The group can be cleaved by a variety of methods, including acid hydrolysis and catalytic hydrogenolysis.