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2,4-Dihydroxybenzaldehyde

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Identification
Molecular formula
C7H6O3
CAS number
95-01-2
IUPAC name
2,4-dihydroxybenzaldehyde
State
State

At room temperature, 2,4-Dihydroxybenzaldehyde is typically found in a solid state. Its crystalline nature makes it stable, and it is not easily disrupted by ambient conditions.

Melting point (Celsius)
150.00
Melting point (Kelvin)
423.15
Boiling point (Celsius)
314.50
Boiling point (Kelvin)
587.65
General information
Molecular weight
138.12g/mol
Molar mass
138.1220g/mol
Density
1.3300g/cm3
Appearence

2,4-Dihydroxybenzaldehyde is a crystalline solid with a color that ranges from light yellow to amber. It often forms needle-like crystals that can aggregate into powdery lumps. The solid is usually free of any significant odor and maintains its integrity under standard conditions.

Comment on solubility

Solubility of 2,4-dihydroxybenzaldehyde

2,4-dihydroxybenzaldehyde, also known as 2,4-Dihydroxybenzaldehyde or salicylaldehyde, exhibits interesting solubility characteristics that are vital for its applications in both industrial and laboratory settings.

Typically, the solubility of this compound can be summarized as follows:

  • Water: 2,4-dihydroxybenzaldehyde is moderately soluble in water due to the presence of hydroxyl groups that can form hydrogen bonds with water molecules.
  • Organic Solvents: It is highly soluble in organic solvents such as ethanol, ether, and chloroform, which enhances its accessibility for various reactions.
  • Temperature Dependence: The solubility may increase with temperature, making it important to consider when conducting reactions.

Considering these factors, it's important to note that the solubility variations can significantly impact the chemical behavior of 2,4-dihydroxybenzaldehyde in different environmental and experimental conditions. As stated in reference literature, “The solubility of compounds like 2,4-dihydroxybenzaldehyde plays a crucial role in determining their reactivity and interactions in solution.”

In conclusion, understanding the solubility of 2,4-dihydroxybenzaldehyde allows chemists to make informed decisions during experimental design and application methodologies.

Interesting facts

Interesting Facts about 2,4-Dihydroxybenzaldehyde

2,4-Dihydroxybenzaldehyde, also known as 2,4-Dihydroxybenzaldehyde or simply salicylaldehyde, is a fascinating compound that has garnered attention in both the fields of organic chemistry and pharmacology. Here are some interesting aspects of this compound:

  • Biological Significance: This compound is a derivative of salicylic acid, which is pivotal in the synthesis of aspirin, a widely used analgesic and anti-inflammatory drug. Its functional groups make it a vital building block in the development of various pharmaceuticals.
  • Flavor and Fragrance: 2,4-Dihydroxybenzaldehyde has a sweet, almond-like aroma. This characteristic makes it valuable in the fragrance and flavor industries, often used to enhance the scent profile of products.
  • Antimicrobial Properties: Some studies have indicated that this compound possesses antimicrobial properties, making it an intriguing subject for further research in developing natural preservatives or treatments for infections.
  • Synthesis: The synthesis of 2,4-dihydroxybenzaldehyde can be achieved through various methods. One common approach is the hydroxylation of benzaldehyde, demonstrating its versatility and applicability in synthetic organic chemistry.
  • Research Applications: Researchers have incorporated 2,4-dihydroxybenzaldehyde in the study of various reactions and processes, including its role as a ligand in coordination chemistry and its potential use in developing innovative materials.
  • Environmental Impact: Given its applications, studying the environmental persistence and biodegradability of this compound is essential to ensure its safe usage and to mitigate possible pollution issues.

In summary, 2,4-dihydroxybenzaldehyde stands out not only for its unique chemical structure but also for its multifaceted applications in diverse fields ranging from medicine to materials science. As research continues to explore its properties and potential applications, the future of this compound looks promising.

Synonyms
2,4-DIHYDROXYBENZALDEHYDE
95-01-2
beta-Resorcylaldehyde
Benzaldehyde, 2,4-dihydroxy-
4-Hydroxysalicylaldehyde
4-Formylresorcinol
beta-Resorcaldehyde
beta-Resorcinaldehyde
beta-Resorcylic aldehyde
b-resorcylaldehyde
.beta.-Resorcylaldehyde
2,4-Dihydroxybenzenecarbonal
beta-Rosorcaldehyde
2,4-Dihydroxybenzaldehyd
Salicylaldehyde, 4-hydroxy-
4-Hydroxysalicyladehyde
MFCD00011686
CHEBI:50198
b-Resorcaldehyde
UNII-772JOF6LZS
b-Resorcinaldehyde
NSC 8690
EINECS 202-383-1
772JOF6LZS
BRN 0878548
b-Resorcylic aldehyde
.beta.-Resorcaldehyde
AI3-24367
.beta.-Resorcinaldehyde
NSC-8690
.beta.-Resorcylic aldehyde
CHEMBL243587
DTXSID8021806
NSC8690
4-08-00-01753 (Beilstein Handbook Reference)
DIHYDROXYBENZALDEHYDE, 2,4-
.BETA.-RESORCYLALDEHYDE [MI]
2,4-Dihydroxybezaldehyde
2,4-dihydroxy benzaldehyde
2,4-dihydroxy-benzaldehyde
Resorcinal
A-Resorcylaldehyde
Beta-resorcyl aldehyde
2,4dihydroxybenzaldehyde
24-Dihydroxybenzaldehyde
2,4-Dihyroxybenzaldehyde
2,4 dihydroxybenzaldehyde
2,4-dihydoxy-benzaldehyde
2,4-dihydroxylbenzaldehyde
2,4,-dihydroxybenzaldehyde
2,4-dihydroxyl benzaldehyde
SCHEMBL93513
MLS001076174
2,4-bis(oxidanyl)benzaldehyde
DTXCID101806
2,4-Dihydroxybenzaldehyde, 98%
HMS2270K22
STR01512
BBL012171
BDBM50140239
STK299744
AKOS000118990
CS-W007539
FD22100
HY-W007539
NCGC00247446-01
AC-24172
PD158252
SMR000639137
SY007063
DB-027606
D0564
NS00040433
EN300-21460
?-Resorcylaldehyde;2,4-Dihydroxybenzenecarbonal
F11148
A845149
AP-065/40195541
Q27121977
F1995-0226
Z104497974
2,4-Dihydroxybenzaldehyde, Vetec(TM) reagent grade, 98%
202-383-1