Interesting facts
Interesting Facts About 2,4,6-Trimethylbenzaldehyde
2,4,6-Trimethylbenzaldehyde, also known as pseudo-vanillin, is a fascinating aromatic compound that derives its name from the presence of three methyl groups at positions 2, 4, and 6 on the benzaldehyde ring. Here are some intriguing facts about this compound:
- Flavor and Fragrance: This compound has a strong vanilla-like aroma, which makes it a popular choice in the food and cosmetics industry. It is often used as a flavoring agent and fragrance component in various products.
- Natural Occurrence: While it is synthetically produced, 2,4,6-trimethylbenzaldehyde can also be found in certain natural sources, particularly in essential oils and extracts of some plants.
- Applications: Beyond its use in flavoring and fragrance, this compound is also applied in organic synthesis. It serves as an important intermediate in the production of various chemicals and can be used to create other complex molecules.
- Research Potential: Due to its unique structure, 2,4,6-trimethylbenzaldehyde is a subject of interest in studies exploring its chemical reactivity and potential therapeutic properties, opening doors to new scientific discoveries.
- Historical Context: The exploration of benzaldehyde derivatives, including 2,4,6-trimethylbenzaldehyde, has been significant in the development of organic chemistry, providing insights into the behavior of aromatic compounds.
In conclusion, 2,4,6-trimethylbenzaldehyde is more than just a simple aldehyde; its wide-ranging applications and pleasant aroma contribute to its prominence in both nature and industry. Its multifaceted nature challenges scientists to continuously explore its properties and potential uses.
Synonyms
2,4,6-TRIMETHYLBENZALDEHYDE
Mesitaldehyde
487-68-3
Mesitylaldehyde
Benzaldehyde, 2,4,6-trimethyl-
Mesitylenecarboxaldehyde
2-Mesitylenecarboxaldehyde
EINECS 207-662-1
NSC 29094
BRN 1364114
4W00MG84DR
DTXSID5052125
AI3-06142
NSC-29094
DTXCID7030694
EC 207-662-1
4-07-00-00730 (Beilstein Handbook Reference)
2Formylmesitylene
2Mesitylenecarboxaldehyde
2Formyl1,3,5trimethylbenzene
Benzaldehyde, 2,4,6trimethyl
207-662-1
inchi=1/c10h12o/c1-7-4-8(2)10(6-11)9(3)5-7/h4-6h,1-3h
2-Formylmesitylene
2,4,6-trimethyl-benzaldehyde
MFCD00003341
2-Formyl-1,3,5-trimethylbenzene
Isodural
mesityl aldehyde
b-Isodural
Aldehydomesitylene
b-Isoduryl aldehyde
Mesitaldehyde - 97%
2,6-Trimethylbenzaldehyde
UNII-4W00MG84DR
SCHEMBL79252
Benzaldehyde,4,6-trimethyl-
CHEMBL3560744
CHEBI:195893
NSC29094
Tox21_303703
AKOS000120393
CS-W018185
FM25113
HY-W017469
NCGC00357022-01
AC-15540
AS-11832
CAS-487-68-3
SY035572
DB-013965
NS00001558
T1368
EN300-20385
Mesitaldehyde, Vetec(TM) reagent grade, 98%
A10762
doi:10.14272/HIKRJHFHGKZKRI-UHFFFAOYSA-N.1
Q63408662
Z104477950
Mesitaldehyde, contains ~0.1% Hydroquinone as stabilizer, 98%
2,4,6-Trimethylbenzaldehyde;2-Formyl-1,3,5-trimethylbenzene;2-Formylmesitylene
Solubility of 2,4,6-trimethylbenzaldehyde
2,4,6-trimethylbenzaldehyde, with its characteristic aromatic structure, displays a notable solubility profile. Being an aromatic aldehyde, it tends to have relatively low polarity, which influences its solubility in various solvents.
Generally, 2,4,6-trimethylbenzaldehyde is:
In summary, the solubility of 2,4,6-trimethylbenzaldehyde reflects its structural characteristics, making it quite useful in various chemical syntheses and applications where solubility in organic media is required.