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β-alanine CAS 107-95-9

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Place of Origin: China

Brand Name: Sunshine

Certification: ISO,COA

Model Number: 107-95-9

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Highlight:
CAS NO::
107-95-9
Appearance::
White Crystals
Molecular Formula::
C3H7NO2
Molecular Weight::
89.09320
EINECS NO::
203-536-5
MDL NO::
MFCD00008200
CAS NO::
107-95-9
Appearance::
White Crystals
Molecular Formula::
C3H7NO2
Molecular Weight::
89.09320
EINECS NO::
203-536-5
MDL NO::
MFCD00008200
β-alanine CAS 107-95-9

Product Description:

Product Name: β-alanine CAS NO: 107-95-9

 

 

Synonyms:

3-Aminopropanoic acid;

beta-alanine;

β-Alanine;

 

 

Chemical & Physical Properties:

Appearance: White crystals. Only naturally occurring beta amino acid.

Assay :≥98.0%

Density: 1.437 g/cm3

Boiling Point: 201℃

Melting Point: 197-202℃

Flash Point: 204-206℃

Stability: Stable. Keep dry.

Storage Condition: Store at RT.

 

 

Safety Information:

Safety Statements: S24/25

Hazard Code: Xi

HS Code: 29224920

WGK Germany: 3

RTECS: UA2369200

Risk Statements: R36/37/38

 

 

β-Alanine (or beta-alanine) is a naturally occurring beta amino acid, which is an amino acid in which the amino group is at the β-position from the carboxylate group (i.e., two atoms away, see Figure 1). The IUPAC name for β-alanine is 3-aminopropanoic acid. Unlike its counterpart α-alanine, β-alanine has no stereocenter.

 

β-Alanine is not used in the biosynthesis of any major proteins or enzymes. It is formed in vivo by the degradation of dihydrouracil and carnosine. It is a component of the naturally occurring peptides carnosine and anserine and also of pantothenic acid (vitamin B5), which itself is a component of coenzyme A. Under normal conditions, β-alanine is metabolized into acetic acid.

 

β-Alanine is the rate-limiting precursor of carnosine, which is to say carnosine levels are limited by the amount of available β-alanine, not histidine. Supplementation with β-alanine has been shown to increase the concentration of carnosine in muscles, decrease fatigue in athletes and increase total muscular work done. Simply supplementing with carnosine is not as effective as supplementing with β-alanine alone since carnosine, when taken orally, is broken down during digestion to its components, histidine and β-alanine. Hence, by weight, only about 40% of the dose is available as β-alanine.

 

L-Histidine, with a pKa of 6.1 is a relatively weak buffer over the physiological intramuscular pH range. However, when bound to other amino acids, this increases nearer to 6.8-7.0. In particular, when bound to β-alanine, the pKa value is 6.83, making this a very efficient intramuscular buffer. Furthermore, because of the position of the beta amino group, β-alanine dipeptides are not incorporated into proteins, and thus can be stored at relatively high concentrations (millimolar). Occurring at 17–25mmol/kg (dry muscle), carnosine (β-alanyl-L-histidine) is an important intramuscular buffer, constituting 10-20% of the total buffering capacity in type I and II muscle fibres.

 

Even though much weaker than glycine (and, thus, with a debated role as a physiological transmitter), β-alanine is an agonist next in activity to the cognate ligand glycine itself, for strychnine-sensitive inhibitory glycine receptors (GlyRs) (the agonist order: glycine ≫ β-alanine > taurine ≫ alanine, L-serine > proline).

 

 

 

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