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1-Hydroxy-6-oxo-1,6-dihydro-pyridine-2-carboxylic acid, commonly known as niacinamide or nicotinamide, is a vital derivative of vitamin B3 that significantly contributes to the metabolism of amino acids and fats. It is integral to energy production within cells and supports the health of the skin, nervous system, and digestive system. With its antioxidant and anti-inflammatory properties, niacinamide has become a prevalent component in skincare products, demonstrating efficacy in enhancing skin texture, reducing the appearance of fine lines and wrinkles, and diminishing hyperpigmentation. Furthermore, it holds potential therapeutic value in addressing conditions such as acne, rosacea, and eczema, establishing 1-Hydroxy-6-oxo-1,6-dihydro-pyridine-2-carboxylic acid as a multifaceted compound with significant implications for both human health and skincare.

94781-89-2

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94781-89-2 Usage

Uses

Used in Skincare Products:
1-Hydroxy-6-oxo-1,6-dihydro-pyridine-2-carboxylic acid is utilized as an active ingredient in skincare products for its ability to improve skin texture, reduce the appearance of fine lines and wrinkles, and fade hyperpigmentation. Its antioxidant and anti-inflammatory properties make it a popular choice for enhancing skin health and appearance.
Used in Therapeutic Applications:
In the medical field, 1-Hydroxy-6-oxo-1,6-dihydro-pyridine-2-carboxylic acid is employed as a potential treatment for various skin conditions, including acne, rosacea, and eczema. Its beneficial properties contribute to the management and improvement of these conditions, offering a natural and effective alternative for skin health.
Used in Nutritional Supplements:
As a derivative of vitamin B3, 1-Hydroxy-6-oxo-1,6-dihydro-pyridine-2-carboxylic acid is used in nutritional supplements to support overall health. It aids in the metabolism of amino acids and fats, contributing to energy production and the maintenance of a healthy nervous and digestive system.
Used in Pharmaceutical Development:
The therapeutic potential of 1-Hydroxy-6-oxo-1,6-dihydro-pyridine-2-carboxylic acid is also recognized in the development of pharmaceuticals. Its antioxidant and anti-inflammatory properties are being explored for the treatment of various conditions, highlighting its versatility and importance in the healthcare industry.

Check Digit Verification of cas no

The CAS Registry Mumber 94781-89-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,7,8 and 1 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 94781-89:
(7*9)+(6*4)+(5*7)+(4*8)+(3*1)+(2*8)+(1*9)=182
182 % 10 = 2
So 94781-89-2 is a valid CAS Registry Number.

94781-89-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Hydroxy-6-oxo-1,6-dihydropyridine-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names 1-hydroxy-6-oxopyridine-2-carboxylic acid

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:94781-89-2 SDS

94781-89-2Upstream product

94781-89-2Relevant academic research and scientific papers

Synthesis of tetradentate mixed bisphosphonates - New hydroxypyridinonate ligands for metal chelation therapy

Bailly, Théodorine,Burgada, Ramon,Prangé, Thierry,Lecouvey, Marc

, p. 189 - 192 (2007/10/03)

In a general study for developing better drugs suitable for Fe, Al, Co or lanthanide chelation therapy experiments, new mixed bisphosphonate-hydroxy pyridonates were synthesized. We demonstrate that the method using amidation reaction and dealkylation by concentrated hydrochloric acid gives excellent results for amino bisphosphonic acid ligands having at least two carbons between the amino group and the methylene bisphosphonic acid group.

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