355387-54-1

Usage

Chemical structure

1,3-Benzenediol, 2,4-dipropyl-

Explanation

1,3-Benzenediol, 2,4-dipropyl- is a derivative of 1,3-benzenediol, with two propyl groups (C3H7) attached to the 2 and 4 positions of the benzene ring.

Explanation

The hydroxyl group is present at the 1 and 3 positions of the benzene ring, while the propyl groups are attached at the 2 and 4 positions.

Explanation

The compound is typically found in a liquid state, with a color ranging from colorless to pale yellow.

Explanation

1,3-Benzenediol, 2,4-dipropylis soluble in organic solvents such as ethanol, methanol, and acetone.

Explanation

1,3-Benzenediol, 2,4-dipropyl- is commonly used in the cosmetic industry for its antioxidant properties, as well as in pharmaceutical products and as a fragrance ingredient in perfumes and personal care products.

Explanation

It is important to handle 1,3-Benzenediol, 2,4-dipropyl- with caution, as it may cause irritation to the skin and eyes. Additionally, it can be harmful if ingested or inhaled in large quantities.

Explanation

To ensure the stability and safety of the compound, it should be stored in a cool, dry, and well-ventilated area, away from sources of heat and open flames.

Explanation

The compound is generally stable under normal temperature and pressure conditions, but it may decompose upon exposure to heat or flame.

Explanation

If released into the environment, 1,3-Benzenediol, 2,4-dipropylmay be harmful to aquatic life due to its chemical properties. Proper disposal and handling are essential to minimize environmental impact.

Functional groups

Hydroxyl (-OH) and propyl (-C3H7)

Appearance

Colorless to pale yellow liquid

Solubility

Soluble in organic solvents

Uses

Cosmetic ingredient, antioxidant, pharmaceutical products, fragrance ingredient

Safety precautions

Potential skin and eye irritant, harmful if ingested or inhaled in large amounts

Storage

Store in a cool, dry, and well-ventilated area, away from heat and open flames

Stability

Stable under normal temperature and pressure conditions

Environmental impact

Potentially harmful to aquatic life

Upstream product

• 13594-95-1 1,3-bis(allyloxy)benzene 
• 108-46-3 recorcinol 
• 13331-19-6 2-propyl-1,3-benzenediol 
• 502-56-7 nonanone-5 
• 705257-43-8 4-allyl-2-propyl-benzene-1,3-diol 
• 705257-21-2 3-allyloxy-2-propyl-phenol 

Downstream Products

• 449779-73-1 1-(2,4-dihydroxy-3,5-dipropyl-phenyl)-propan-1-one 
• 860780-47-8 ethyl 4-nitroso-2,6-dipropyl-1,3-phenylene biscarbonate 
• 1000841-84-8 3-(tert-butyldimethylsilyloxy)-2,6-di-propylphenol 
• 1186118-36-4 1,5-dimethyl-3-(4-(2-oxo-6,8-di-n-propyl-4-(trifluoromethyl)-2H-chromen-7-yloxy)butyl)-5-phenylimidazolidine-2,4-dione 
• 1186118-03-5 5-methyl-3-(4-(2-oxo-6,8-di-n-propyl-4-(trifluoromethyl)-2H-chromen-7-yloxy)-butyl)-5-phenylimidazolidine-2,4-dione 
• 1186118-11-5 5-methyl-3-(4-(2-oxo-6,8-di-n-propyl-4-(trifluoromethyl)-2H-chromen-7-yloxy)-butyl)-5-p-tolylimidazolidine-2,4-dione 
• 1186118-04-6 5-(2-methoxyphenyl)-5-methyl-3-(4-(2-oxo-6,8-di-n-propyl-4-(trifluoromethyl)-2H-chromen-7-yloxy)butyl)imidazolidine-2,4-dione 
• 1186118-05-7 5-(4-methoxyphenyl)-5-methyl-3-(4-(2-oxo-6,8-di-n-propyl-4-(trifluoromethyl)-2H-chromen-7-yloxy)butyl)imidazolidine-2,4-dione 
• 1186118-06-8 5-(4-methoxyphenyl)-5-methyl-3-(4-(2-oxo-6,8-di-n-propyl-4-(trifluoromethyl)-2H-chromen-7-yloxy)butyl)imidazolidine-2,4-dione 
• 1186118-22-8 5-(3,4-dimethoxyphenyl)-5-methyl-3-(4-(2-oxo-6,8-di-n-propyl-4-(trifluoromethyl)-2H-chromen-7-yloxy)butyl)imidazolidine-2,4-dione 
• 1186118-18-2 5-(4-(dimethylamino)phenyl)-5-methyl-3-(4-(2-oxo-6,8-di-n-propyl-4-(trifluoromethyl)-2H-chromen-7-yloxy)butyl)imidazolidine-2,4-dione 
• 1186116-20-0 5-methyl-3-(4-(2-oxo-6,8-di-n-propyl-4-(trifluoromethyl)-2H-chromen-7-yloxy)butyl)-5-(4-(trifluoromethyl)phenyl)imidazolidine-2,4-dione 
• 1186118-17-1 5-methyl-5-(4-nitrophenyl)-3-(4-(2-oxo-6,8-di-n-propyl-4-(trifluoromethyl)-2H-chromen-7-yloxy)butyl)imidazolidine-2,4-dione 
• 1186118-21-7 4-(4-methyl-2,5-dioxo-1-(4-(2-oxo-6,8-di-n-propyl-4-(trifluoromethyl)-2H-chromen-7-yloxy)butyl)imidazolidin-4-yl)benzoic acid 

Relevant academic research and scientific papers

A regioselective synthesis of 2,4-dialkyl resorcinols

A general regioselective synthesis of 2,4-dialkyl resorcinols from ethoxymethylenemalonate ethyl ester and dialkyl ketones is reported.

Design and discovery of 2-oxochromene derivatives as liver X receptor β-selective agonists

In an attempt to molecularly design liver X receptor (LXR) β-selective agonists, we discovered that the combination of the 2-oxochromene moiety (head) and the imidazoline-2,4-dione moiety (tail) plays an important role in the expression potency and select

Discovery of a novel series of peroxisome proliferator-activated receptor α/γ dual agonists for the treatment of type 2 diabetes and dyslipidemia

A series of 2-aryloxy-2-methyl-propionic acid compounds and related analogues were designed, synthesized, and evaluated for their PPAR agonist activities. 2-[(5,7-Dipropyl-3-trifluoromethyl)-benzisoxazol-6-yloxy]-2- methylpropionic acid (4) was identified

Aryloxyacetic acids for diabetes and lipid disorders

A class of aryloxyacetic acids comprises compounds that are potent agonists of PPAR alpha and/or gamma, and are therefore useful in the treatment, control or prevention of non-insulin dependent diabetes mellitus (NIDDM), hyperglycemia, dyslipidemia, hyper

O-Arylmandelic acids as highly selective human PPAR α/γ agonists

A new class of O-arylmandelic acid PPAR agonists show excellent anti-hyperglycemic efficacy in a db/db mouse model of DM2. These PPARα-weighted agonists do not show the typical PPARγ associated side effects of BAT proliferation and cardiac hypertrophy in

Aryloxyacetic acids for diabetes and lipid disorders

A class of aryloxyacetic acids comprises compounds that are potent agonists of PPAR alpha and/or gamma, and are therefore useful in the treatment, control or prevention of non-insulin dependent diabetes mellitus (NIDDM), hyperglycemia, dyslipidemia, hyper