6280-15-5

Usage

Uses

Used in Chemical Synthesis:
3-Methylpentanedial is used as an intermediate in the synthesis of other organic compounds, leveraging its reactive aldehyde group to form a range of derivatives, which contribute to the development of various chemical products.
Used in the Dye Industry:
3-Methylpentanedial is used as a solvent in the production of dyes, where its solubility properties aid in the manufacturing process, enhancing the colorfastness and quality of the final dye products.
Used in the Perfume Industry:
In the perfume industry, 3-Methylpentanedial is utilized as a solvent for creating fragrances, taking advantage of its ability to dissolve a wide range of aromatic compounds, which contributes to the complexity and longevity of scents.
Used in the Pharmaceutical Industry:
3-Methylpentanedial serves as a solvent in the production of pharmaceuticals, playing a crucial role in the formulation of medications, where its properties can influence the solubility, stability, and bioavailability of active pharmaceutical ingredients.
Overall, 3-Methylpentanedial is a multifaceted chemical with applications across several industries, from chemical synthesis to the creation of dyes, perfumes, and pharmaceuticals. Its use, however, must be managed with an awareness of its potential toxicity to ensure the safety of both handlers and consumers.

InChI:InChI=1/C6H10O2/c1-6(2-4-7)3-5-8/h4-6H,2-3H2,1H3

Upstream product

• 75-07-0 acetaldehyde 
• 1118-59-8 3-methylbut-3-en-1-al 
• 4457-71-0 3-methylpentane-1,5-diol 
• 626-58-4 4-methylpiperidin 
• 10138-44-0 2-ethoxy-4-methyl-3,4-dihydro-2H-pyran 
• 38113-08-5 3,4-dihydro-2-methoxy-4-methyl-2H-pyran 

Downstream Products

• 16855-95-1 4-methyl-4H-pyran 
• 1428771-11-2 C₂₆H₂₉NO₅ 
• 4457-72-1 3-methyl-1,5-dibromopentane 
• 114472-85-4 <(1R,2R,3S,5R)-3-acetoxy-5-methyl-2-nitrocyclohexyl>-pivalat 
• 114454-97-6 <(1R,2R,3S,5R)-3-hydroxy-5-methyl-2-nitrocyclohexyl>-pivalat 
• 4457-71-0 3-methylpentane-1,5-diol 
• 4166-53-4 3-methylglutaric anhydride 
• 626-51-7 3-methyl glutaric acid 
• 108-89-4 picoline 

Relevant academic research and scientific papers

METHOD FOR PRODUCING ALDEHYDE COMPOUND, AND ACETAL COMPOUND

Provided are a method for producing 3-methylglutaraldehyde in a good yield under a mild condition and a novel acetal compound which is useful for carrying out the foregoing method. The method is a production method of 3-methylglutaraldehyde including a step of hydrolyzing a compound represented by the following general formula (1): wherein R1 and R2 each independently represent an alkyl group having 1 to 6 carbon atoms, or are mutually coupled to represent an alkylene group having 2 to 6 carbon atoms.

N-[3-(2-CARBOXYETHYL)PHENYL]PIPERIDIN-1-YLACETAMIDE DERIVATIVES AND USE THEREOF AS ACTIVATORS OF SOLUBLE GUANYLATE CYCLASE

The present application relates to novel substituted 2-(piperidin-1-yl)acetamide derivatives, to processes for preparation thereof, to the use thereof for treatment and/or prevention of diseases, and to the use thereof for production of medicaments for treatment and/or prevention of diseases, especially for treatment and/or prevention of cardiovascular diseases.

Nicotinium dichromate (= 3-carboxypyridinium dichromate; NDC) as an efficient reagent for the oxidative deamination of amines and aminophosphonates

A new method for the efficient synthesis of aldehydes, ketones, and oxophosphonates from various types of amines (primary and secondary) and aminophosphonates via oxidative deamination by nicotinium dichromate (= 3-carboxypyridinium dichromate; NDC) is described.

Oxidative deamination of α-aminophosphonates and amines by zinc dichromate trihydrate (ZnCr2O73H2O) under solvent-free conditions at room temperature

A novel method for the rapid and efficient conversion of a variety of -aminophosphonates to α-ketophosphonates using ZnCr2O 73H2O via oxidative deamination under solvent-free conditions at room temperature is described. This method is also applicable to the rapid and highly selective oxidation of various types of ordinary amines (primary and secondary) to aldehydes and ketones in good to high yields. Georg Thieme Verlag Stuttgart New York.