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1818-66-2

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1818-66-2 Usage

Description

1,3,7-trimethyl-8-propoxy-3,7-dihydro-1H-purine-2,6-dione, commonly known as caffeine, is a naturally occurring chemical compound that serves as a central nervous system stimulant. It is found in various plant sources such as coffee beans, tea leaves, and cacao pods. Caffeine is widely consumed as a psychoactive drug and a mild diuretic, and it is an active ingredient in many popular beverages, including coffee, tea, and energy drinks. Its stimulant effects are due to its ability to block adenosine receptors in the brain, resulting in increased alertness and energy levels. Additionally, caffeine has known effects on metabolism, athletic performance, and cognitive function. However, excessive consumption can lead to negative side effects such as insomnia, anxiety, and heart palpitations.

Uses

Used in Beverage Industry:
1,3,7-trimethyl-8-propoxy-3,7-dihydro-1H-purine-2,6-dione is used as a stimulant and flavoring agent in the beverage industry for its ability to increase alertness and energy levels, as well as for enhancing the taste of coffee, tea, and energy drinks.
Used in Pharmaceutical Industry:
Caffeine is used as an active ingredient in various pharmaceutical products for its stimulant effects, including medications for migraine relief, alertness enhancement, and as a component in combination drugs to treat nasal congestion and other respiratory issues.
Used in Sports Nutrition:
1,3,7-trimethyl-8-propoxy-3,7-dihydro-1H-purine-2,6-dione is used as a performance-enhancing substance in sports nutrition for its ability to improve athletic performance by increasing alertness, reducing fatigue, and boosting energy levels.
Used in Cognitive Function Enhancement:
Caffeine is used as a cognitive function enhancer, particularly for improving focus, concentration, and memory, making it a popular choice for students, professionals, and individuals seeking to improve their cognitive abilities.
Used in Metabolism Regulation:
1,3,7-trimethyl-8-propoxy-3,7-dihydro-1H-purine-2,6-dione is used as a metabolism regulator, helping to increase the metabolic rate and promote weight loss or maintain a healthy weight by stimulating the breakdown of fats and carbohydrates.
Used in Sleep Aid Products:
Although caffeine is known for its stimulant effects, it is also used in some sleep aid products in combination with other ingredients to promote relaxation and improve sleep quality when consumed in lower doses or in specific formulations.

Check Digit Verification of cas no

The CAS Registry Mumber 1818-66-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,1 and 8 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1818-66:
(6*1)+(5*8)+(4*1)+(3*8)+(2*6)+(1*6)=92
92 % 10 = 2
So 1818-66-2 is a valid CAS Registry Number.

1818-66-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3,7-trimethyl-8-propoxypurine-2,6-dione

1.2 Other means of identification

Product number -
Other names 8-Propyloxycaffeine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1818-66-2 SDS

1818-66-2Downstream Products

1818-66-2Relevant articles and documents

Electrochemical C?H Functionalization of (Hetero)Arenes—Optimized by DoE

D?rr, Maurice,R?ckl, Johannes L.,Rein, Jonas,Schollmeyer, Dieter,Waldvogel, Siegfried R.

supporting information, p. 10195 - 10198 (2020/07/04)

A novel approach towards the activation of different arenes and purines including caffeine and theophylline is presented. The simple, safe and scalable electrochemical synthesis of 1,1,1,3,3,3-hexafluoroisopropanol (HFIP) aryl ethers was conducted using an easy electrolysis setup with boron-doped diamond (BDD) electrodes. Good yields up to 59 percent were achieved. Triethylamine was used as a base as it forms a highly conductive media with HFIP, making additional supporting electrolytes superfluous. The synthesis was optimized using Design of Experiment (DoE) techniques giving a detailed insight to the significance of the reaction parameters. The mechanism was investigated by cyclic voltammetry (CV). Subsequent transition metal-catalyzed as well as metal-free functionalization led to interesting motifs in excellent yields up to 94 percent.

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