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222402

Methylguanidine hydrochloride

Name: Methylguanidine hydrochloride
Brand: ALDRICH

98%

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About This Item

Formule linéaire :

CH₃NHC(=NH)NH₂·HCl

Numéro CAS:

21770-81-0

Poids moléculaire :

109.56

Numéro MDL:

MFCD00012576

Code UNSPSC :

12352100

ID de substance PubChem :

24853329

Nomenclature NACRES :

NA.22

Pureté

98%

Forme

solid

Solubilité

water: soluble 50 mg/mL, clear

Chaîne SMILES

Cl.CNC(N)=N

InChI

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

Clé InChI

VJQCNCOGZPSOQZ-UHFFFAOYSA-N

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Catégories apparentées

Synthons (building blocks)

Synthons organiques

Application

Methylguanidine hydrochloride can be used to prepare:

Biaryl derivatives as BACE1 inhibitors.
Modified xylose, which is used in the synthesis of biodegradable composite hydrogels.
Methylguanidinium borohydride ionic liquid, which is applicable as a hydrogen storage material.

Pictogrammes

GHS07

Mention d'avertissement

Warning

Mentions de danger

H302,H315,H319

Conseils de prudence

P264 - P280 - P301 + P312 - P302 + P352 - P305 + P351 + P338 - P332 + P313

Classification des risques

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

dust mask type N95 (US), Eyeshields, Gloves

Certificats d'analyse (COA)

Recherchez un Certificats d'analyse (COA) en saisissant le numéro de lot du produit. Les numéros de lot figurent sur l'étiquette du produit après les mots "Lot" ou "Batch".

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Sigma-Aldrich

G4505

Guanidine hydrochloride

Sigma-Aldrich

254134

Chlorure d′ammonium

A non-covalent strategy for montmorillonite/xylose self-healing hydrogels

Qi X, et al.

Royal Society of Chemistry Advances, 5(51), 41006-41012 (2015)

Structure based design of iminohydantoin BACE1 inhibitors: identification of an orally available, centrally active BACE1 inhibitor.

Jared N Cumming et al.

Bioorganic & medicinal chemistry letters, 22(7), 2444-2449 (2012-03-07)

From an initial lead 1, a structure-based design approach led to identification of a novel, high-affinity iminohydantoin BACE1 inhibitor that lowers CNS-derived Aβ following oral administration to rats. Herein we report SAR development in the S3 and F' subsites of

Interactions of Protonated Guanidine and Guanidine Derivatives with Multiply Deprotonated RNA Probed by Electrospray Ionization and Collisionally Activated Dissociation.

Jovana Vušurović et al.

ChemistryOpen, 6(6), 739-750 (2017-12-12)

Interactions of ribonucleic acid (RNA) with guanidine and guanidine derivatives are important features in RNA-protein and RNA-drug binding. Here we have investigated noncovalently bound complexes of an 8-nucleotide RNA and six different ligands, all of which have a guanidinium moiety

Structure and dynamics of a salt-bridge model system in water and DMSO.

S Lotze et al.

The Journal of chemical physics, 142(21), 212436-212436 (2015-06-08)

We study the interaction between the ions methylguanidinium and trifluoroacetate dissolved in D2O and dimethylsulfoxide with linear infrared spectroscopy and femtosecond two-dimensional infrared spectroscopy. These ions constitute model systems for the side chains of arginine and glutamic and aspartic acid

In-vitro evidence of enhanced breast cancer resistance protein-mediated intestinal urate secretion by uremic toxins in Caco-2 cells.

Yang Lu et al.

The Journal of pharmacy and pharmacology, 67(2), 170-177 (2014-12-18)

It has been reported that intestinal urate excretion is increased at chronic kidney disease (CKD) state. In this report, whether uremic toxins are involved in the upregulation of intestinal breast cancer resistance protein (BCRP), an intestinal urate exporter, was examined.

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