Veratraldehyde | Solubility of Things

Identification

Molecular formula

C₉H₁₀O₃

CAS number

120-14-9

IUPAC name

3,4-dimethoxybenzaldehyde

State

At room temperature, veratraldehyde is in a solid state, specifically as crystalline solid or powder. It is important to handle it in appropriate conditions to maintain its solid-state integrity.

Melting point (Celsius)

43.00

Melting point (Kelvin)

316.00

Boiling point (Celsius)

281.00

Boiling point (Kelvin)

554.00

General information

Molecular weight

166.17g/mol

Molar mass

166.1730g/mol

Density

1.1527g/cm³

Appearence

Veratraldehyde appears as a white to pale yellow crystalline solid. It may also appear as an off-white powder and has a characteristic pleasant aromatic odor. Due to its crystalline nature, it has a defined solid structure at room temperature.

Comment on solubility

Solubility of 3,4-Dimethoxybenzaldehyde

3,4-dimethoxybenzaldehyde, with the chemical formula C₉H₁₀O₃, is an intriguing organic compound known for its distinct solubility characteristics. Here are some key points regarding its solubility:

Polar Solvents: This compound exhibits good solubility in polar solvents like methanol and ethanol due to the presence of the functional aldehyde group and methoxy substituents.
Non-Polar Solvents: It shows moderate solubility in non-polar solvents such as hexane and benzene, although the solubility is considerably less than in polar solvents.
Water: 3,4-dimethoxybenzaldehyde is sparingly soluble in water. The relatively hydrophobic nature of the aromatic ring and the methoxy groups limits its interaction with water molecules.

In summary, the solubility of 3,4-dimethoxybenzaldehyde reflects a balance between its polar and non-polar properties, which can be attributed to its unique structural features. As the saying goes, "like dissolves like," and understanding this principle is crucial for predicting the compound's behavior in various solvents.

Interesting facts

Interesting Facts about 3,4-Dimethoxybenzaldehyde

3,4-Dimethoxybenzaldehyde is a fascinating compound that belongs to the family of aromatic aldehydes. This compound is not only valued for its chemical properties but also has intriguing applications across various fields, particularly in organic synthesis and fragrance formulation. Here are some captivating aspects of this compound:

Fragrance Component: The compound is often used as a fragrance ingredient in perfumes due to its pleasant aromatic profile. It adds warmth and complexity to fragrances, making it a favorite among perfumers.
Organic Synthesis: In the realm of organic chemistry, 3,4-dimethoxybenzaldehyde serves as a vital intermediate in the synthesis of other pharmaceutical compounds and natural products. Its functional groups allow for versatile chemical reactions, including nucleophilic additions and condensation reactions.
Biological Activity: There have been studies indicating that related compounds might exhibit significant biological activities, such as antioxidant or antimicrobial effects. This opens up potential avenues for future research concerning the medicinal properties of 3,4-dimethoxybenzaldehyde and its derivatives.
Structure-Activity Relationship: The specific arrangement of the methoxy groups on the benzene ring plays a crucial role in dictating the reactivity and properties of the compound. Understanding this relationship can help chemists design new compounds tailored for specific applications.
Safety Considerations: As with many organic compounds, proper handling and safety precautions should be observed. Always consult safety data sheets (SDS) when working with this compound to understand its hazards.

The study of 3,4-dimethoxybenzaldehyde not only enhances our comprehension of chemical reactivity but also emphasizes its significance in real-world applications. As noted by chemists, "The beauty of chemistry lies in its ability to create something magnificent from simple building blocks." Indeed, 3,4-dimethoxybenzaldehyde exemplifies this principle!

Synonyms

3,4-Dimethoxybenzaldehyde

VERATRALDEHYDE

120-14-9

Veratric aldehyde

Methylvanillin

Benzaldehyde, 3,4-dimethoxy-

Vanillin methyl ether

Veratral

4-O-Methylvanillin

Veratrum aldehyde

Veratryl aldehyde

p-Veratric aldehyde

3,4-Dimethoxy benzaldehyde

3,4-Dimethoxybenzenecarbonal

Protocatechualdehyde dimethyl ether

Protocatechuic aldehyde dimethyl ether

3,4-DIMETHOXY-BENZALDEHYDE

MFCD00003363

Protocatechuecaldehyde dimethyl ether

NSC 24521

FEMA No. 3109

CCRIS 6285

UNII-UI88P68JZD

EINECS 204-373-2

UI88P68JZD

BRN 0473899

DTXSID7026285

CHEBI:17098

AI3-08099

NSC-8500

NSC-24521

VERATRALDEHYDE [MI]

3, 4-Dimethoxybenzaldehyde

VERATRALDEHYDE [FCC]

VERATRALDEHYDE [FHFI]

DTXCID406285

Benzaldehyde,4-dimethoxy-

WLN: VHR CO1 DO1

VERAPAMIL HYDROCHLORIDE IMPURITY G [EP IMPURITY]

Methyl vanillin

CAS-120-14-9

VERAPAMIL HYDROCHLORIDE IMPURITY G (EP IMPURITY)

veratrumald

ratryl aldehyde

Veratrumaldehyde

FEMA 3109

3,4-dimethoxy

3,4dimethoxybenzaldehyde

3,4-dimethoxybenzaldehyde (veratraldehyde)

3,4-dimethoxybenzaldeyde

3,4 dimethoxybenzaldehyde

3,4-dimethoxybenzaidehyde

4,3-dimethoxybenzaldehyde

4,5-dimethoxybenzaldehyde

40-METHYLVANILLIN

bmse010220

SCHEMBL25202

Veratraldehyde, >=98%, FG

CHEMBL1088937

MSK3363

NSC8500

3,4-Dimethoxybenzaldehyde, 99%

HY-N1096

NSC24521

Tox21_201566

Tox21_303074

BBL010373

s3214

STK188425

AKOS000118989

CS-W019906

Dimethoxy-Benzaldehyde-O-Methylvanillin

FD54842

NCGC00091642-01

NCGC00091642-02

NCGC00091642-03

NCGC00257217-01

NCGC00259115-01

AC-10201

AC-34441

AS-11996

SY004136

Benzaldehyde, 3,4-dimethoxy-veratraldehyde

Veratraldehyde (3,4-Dimethoxybenzaldehyde)

DB-014213

D0507

NS00013328

EN300-16145

C02201

AH-034/32845024

Q414395

Z53837671

F2190-0618

204-373-2