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Propanamide, 2-amino-3-hydroxy-, also known as beta-alanine or 3-aminopropanoic acid, is a non-essential amino acid with the chemical formula C3H9NO2. It is a component of the dipeptide carnosine, which possesses antioxidant properties and is abundant in muscle tissue. Beta-alanine supplementation can increase muscle carnosine levels, potentially enhancing exercise performance and delaying muscle fatigue. It also has potential therapeutic applications in conditions such as diabetes and Parkinson's disease.

25739-59-7

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25739-59-7 Usage

Uses

Used in Sports Nutrition:
Propanamide, 2-amino-3-hydroxyis used as a dietary supplement for enhancing exercise performance and delaying muscle fatigue. The increased muscle carnosine levels resulting from beta-alanine supplementation can improve physical endurance and reduce muscle soreness during high-intensity workouts.
Used in Pharmaceutical Industry:
Propanamide, 2-amino-3-hydroxyis used as a potential therapeutic agent for managing conditions such as diabetes and Parkinson's disease. Its antioxidant properties and ability to increase muscle carnosine levels may contribute to the management and treatment of these conditions.
Used in Cosmetics Industry:
Propanamide, 2-amino-3-hydroxyis used as an ingredient in cosmetic products for its antioxidant properties. It may help protect the skin from oxidative stress and support skin health by maintaining the integrity of collagen and elastin fibers.

Check Digit Verification of cas no

The CAS Registry Mumber 25739-59-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,7,3 and 9 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 25739-59:
(7*2)+(6*5)+(5*7)+(4*3)+(3*9)+(2*5)+(1*9)=137
137 % 10 = 7
So 25739-59-7 is a valid CAS Registry Number.

25739-59-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name Serinamide

1.2 Other means of identification

Product number -
Other names Hydroxy-2-amino-3-phenazin

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:25739-59-7 SDS

25739-59-7Downstream Products

25739-59-7Relevant academic research and scientific papers

2-PYRIDYL CARBOXAMIDE-CONTAINING SPLEEN TYROSINE KINASE (SYK) INHIBITORS

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Paragraph 00167, (2014/10/04)

The invention provides certain 2-pyridyl carboxamide-containing compounds of the Formula (I) or pharmaceutically acceptable salts thereof, wherein A and B are as defined herein. The invention also provides pharmaceutical compositions comprising such compounds, and methods of using the compounds for treating diseases or conditions mediated by Spleen Tyrosine Kinase (Syk) kinase.

Derivatives of antibiotic GE2270 factors C2a, D2 and E

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, (2008/06/13)

Mono- or di-substituted derivatives of GE2270 factors C2a, D2 and E of general formula (I), wherein W represents a moiety of formula (a), (b) or (c), R1 and R2 representing a variety of substituents, X1 is methyl, X2 is a --CH2 --W1 moiety and X3 is methylamino or amino, or X1 is a --CH2 --W1 moiety, X2 is methoxymethylene and X3 is methylamino, with the proviso that when X3 is amino, then W must be 2-(aminocarbonyl)-pyrrolidinyl; with the further proviso that when W is 2-(aminocarbonyl)-pyrrolidinyl, then W1 cannot be hydroxy; and the pharmaceutically acceptable salts thereof. The mono- or di-substituted derivatives of antibiotic GE 2270 of formula (I) are antimicrobial agents mainly active against gram positive bacteria. STR1

Carbamoyl substituted heterocycles

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, (2008/06/13)

This invention relates to carbamoyl substituted heterocycles which are ω-phenyl-ω-(3-pyridyl)-ω-alkenoic acid derivatives bearing a carbamoyl substituted oxazolyl or oxazolinyl group on the phenyl ring and which demonstrate utility for thromboxane receptor antagonism and/or thromboxane synthase inhibition, as well as pharmaceutical formulations containing them, methods for their use, and processes and intermediates for their preparation.

Preparation of substituted alkenoic acids

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, (2008/06/13)

This invention relates to a highly selective process for preparation of E-ω-phenyl-ω-(3-pyridyl)-ω-alkenoic acid derivatives bearing a carbamoyl substituted oxazolyl or oxazolinyl group on the phenyl ring which demonstrate utility for thromboxane receptor antagonism and/or thromboxane synthase inhibition, as well as to intermediates therefor.

PREPARATION OF SUBSTITUTED ALKENOIC ACIDS

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, (2008/06/13)

This invention relates to a highly selective process for preparation of E-ω-phenyl-ω-(3-pyridyl)-ω-alkenoic acid derivatives bearing a carbamoyl substituted oxazolyl or oxazolinyl group on the phenyl ring which demonstrate utility for thromboxane receptor antagonism and/or thromboxane synthase inhibition, as well as to intermediates therefor.

Carbamoyl substituted oxazoles as thromboxane receptor antagonists

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, (2008/06/13)

This invention relates to carbamoyl substituted heterocycles which are ω-phenyl-ω-(3-pyridyl)-ω-alkenoic acid derivatives bearing a carbamoyl substituted oxazolyl or oxazolinyl group on the phenyl ring and which demonstrate utility for thromboxane receptor antagonism and/or thromboxane synthase inhibition, as well as pharmaceutical formulations containing them, methods for their use, and processes and intermediates for their preparation.

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