CAS 22661-87-6

Guanidine, methyl-, hydrochloride

Description:

Methyl guanidine hydrochloride, with the CAS number 22661-87-6, is an organic compound characterized by its guanidine structure, which features a central carbon atom bonded to two amino groups and a methyl group. This compound typically appears as a white crystalline solid and is soluble in water, making it useful in various chemical applications. Methyl guanidine hydrochloride is often utilized in biochemical research and as a reagent in organic synthesis due to its ability to act as a strong base and nucleophile. It can participate in various chemical reactions, including the formation of guanidine derivatives and other nitrogen-containing compounds. Additionally, it has been studied for its potential biological activities, including its effects on cellular processes. However, like many chemical substances, it should be handled with care, as it may pose health risks if ingested or inhaled. Proper safety protocols should be followed when working with this compound in laboratory settings.

Formula: C₂H₇N₃·xClH

InChI: InChI=1S/C2H7N3.ClH/c1-5-2(3)4;/h1H3,(H4,3,4,5);1H

InChI key: InChIKey=VJQCNCOGZPSOQZ-UHFFFAOYSA-N

SMILES: C(NC)(=N)N.Cl

Synonyms:

• (E)-amino(imino)-N-methylmethanaminium chloride
• Guanidine, methyl-, hydrochloride
• Methylguanidine Hydrochloride
• 1-methylguanidine hydrochloride

1-Methylguanidine hydrochloride(1:x)

CAS: 22661-87-6

Formula: C₂H₈ClN₃

Purity: 97%

Color and Shape: Solid

Molecular weight: 109.5580

Ref: IN-DA00BBQD

1-Methylguanidine HCl

CAS: 22661-87-6

1-Methylguanidine HCl is a denaturing agent that has been used in the determination of nitrogen atoms in organic compounds. It has also been shown to have biological properties, such as anti-inflammatory activity and modulation of nitric oxide synthase. 1-Methylguanidine HCl is used in medicine as an anti-inflammatory drug, but it is not currently approved for medical use. 1-Methylguanidine HCl may be used therapeutically to reduce serum levels of creatine, which is synthesized in the liver and excreted by the kidney.

Purity: Min. 95%

Ref: 3D-FM39709