GABA (Gamma Aminobutyric Acid)

Gamma-aminobutyric acid (GABA) is a non-proteinogenic amino acid that serves as the primary inhibitory neurotransmitter in the mammalian central nervous system. It plays a pivotal role in regulating neuronal activity by reducing the excitability of neurons, which contributes to its calming effects and its ability to mitigate anxiety, stress, and fear. GABA is synthesized from glutamate by the enzyme glutamic acid decarboxylase and acts on specific GABA receptors in the brain, namely GABA-A and GABA-B receptors, to decrease the responsiveness of nerve cells.

The health benefits associated with GABA are vast and include its potential to alleviate symptoms of anxiety and mood disorders, as well as its association with the regulation of sleep patterns, which can be beneficial for those suffering from insomnia. Additionally, GABA has been linked to the management of high blood pressure, diabetes, and certain neurological conditions such as epilepsy.

Research also suggests that GABA may have anti-hypertensive, anti-diabetic, anti-cancer, antioxidant, anti-inflammatory, and anti-microbial properties, highlighting its potential in a wide range of pharmaceutical applications. Furthermore, GABA has been found to offer hepato-protective, reno-protective, and intestinal protective effects, indicating its broad therapeutic potential.

It’s important to note that while GABA is naturally present in some foods and available as a supplement, the efficacy of oral GABA, particularly in crossing the blood-brain barrier, has been a subject of debate. However, some studies suggest that oral GABA may still exert effects on the peripheral nervous system and through the gut-brain axis, which could contribute to its overall health benefits.

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Description

Gamma-aminobutyric acid (GABA) is a non-proteinogenic amino acid that serves as the primary inhibitory neurotransmitter in the mammalian central nervous system. It plays a pivotal role in regulating neuronal activity by reducing the excitability of neurons, which contributes to its calming effects and its ability to mitigate anxiety, stress, and fear. GABA is synthesized from glutamate by the enzyme glutamic acid decarboxylase and acts on specific GABA receptors in the brain, namely GABA-A and GABA-B receptors, to decrease the responsiveness of nerve cells.

The health benefits associated with GABA are vast and include its potential to alleviate symptoms of anxiety and mood disorders, as well as its association with the regulation of sleep patterns, which can be beneficial for those suffering from insomnia. Additionally, GABA has been linked to the management of high blood pressure, diabetes, and certain neurological conditions such as epilepsy.

Research also suggests that GABA may have anti-hypertensive, anti-diabetic, anti-cancer, antioxidant, anti-inflammatory, and anti-microbial properties, highlighting its potential in a wide range of pharmaceutical applications. Furthermore, GABA has been found to offer hepato-protective, reno-protective, and intestinal protective effects, indicating its broad therapeutic potential.

Product Name: GABA
Synonyms: γ-Aminobutyric acid
CAS#: 56-12-2
Molecular Formula: C4H9NO2
Molecular Weight: 103.12
ItemStandard
AppearanceWhite to off-white crystals or crystalline powder
State of solutionClear
IdentificationPositive
Chloride (Cl)Not more than 0.020%
Sulfate (SO4)Not more than 0.020%
Heavy metal(Pb)Not more than 10ppm
Arsenic(As2O3)Not more than 1ppm
Loss on dryingNot more than 0.30%
ResidueonignitionNot more than 0. 10%
AssayNot less than 99.0%
LeadNot more than 0.5ppm
MercuryNot more than 0. 1ppm
Melting Range197~204℃
Residual SolventsNegative(α-pyrrolidone)
pH6.5 to 7.5
Total Plate Count cfu//g<1000cfu/g
Yeast & Mold cfu/g<100 cfu/g
E.ColiNegative
SalmonellaNegative
Staphylococcus AureusNegative
Coliform<100 cfu/g
Bulk density0.30~0.52g/ml
Tap density0.50~0.68g/ml
Particle Size100% pass 30 mesh

Additional information

Appearance

White or off-white powder

Package

25 KG PAPER DRUM

MOQ

25KG-1000KG

Production standards

USP

CAS. NO.

1956-12-2