BETAINE ANHYDROUS

Betaine (trimethylglycine) acts as a methyl donor supporting liver function and homocysteine metabolism. Side effects are minimal and may include GI upset. Only GMP materials will be supplied, logistics all according to GDP.

SKU: f71842a388f4 Category: Tag:

Product Description


Mechanism of action

Betaine (trimethylglycine) is a naturally occurring osmolyte and methyl-group donor. It functions as an organic osmoprotectant by stabilising protein structure and maintaining cellular hydration during osmotic stress. In its methylation role, betaine donates a methyl group to homocysteine via betainehomocysteine methyltransferase, forming methionine and supporting the methionine cycle and S-adenosylmethionine (SAM) synthesis.

Benefits and advantages

A key compound in methylation research, hepatic metabolism studies, osmotic-stress models, and nutritional biochemistry. Used to investigate homocysteine regulation, epigenetic methylation capacity, and hepatic lipid accumulation dynamics. Also a valuable standard in cell-volume regulation and osmotic adaptation assays.

Side effects and risks

Generally well tolerated but high doses may cause gastrointestinal discomfort, mild nausea, or electrolyte shifts. Handle as a hygroscopic biochemical with appropriate moisture protection.

Only GMP materials will be supplied, logistics all according to GDP.

Datasheet


Molecular Formula

C5H11NO2

Molecular Weight

117.15 g/mol

CAS Number

107-43-7

Storage Condition

Store below 40 °C (104 °F), preferably between 15 and 30 °C (59 and 86 °F), unless otherwise specified by the manufacturer . Protect from moisture .

Solubility

Soluble

Purity

Purity information is available upon request (COA).

Synonym

betaine; 107-43-7; glycine betaine; Trimethylglycine; oxyneurine

IUPAC/Chemical Name

2-(trimethylazaniumyl)acetate

InChl Key

KWIUHFFTVRNATP-UHFFFAOYSA-N

InChl Code

InChI=1S/C5H11NO2/c1-6(2,3)4-5(7)8/h4H2,1-3H3

References

https://pubchem.ncbi.nlm.nih.gov/compound/247;

3D Conformer.

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