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222402

Sigma-Aldrich

Methylguanidine hydrochloride

98%

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About This Item

Linear Formula:
CH3NHC(=NH)NH2·HCl
CAS Number:
21770-81-0
Molecular Weight:
109.56
MDL number:
MFCD00012576
UNSPSC Code:
12352100
PubChem Substance ID:
24853329
NACRES:
NA.22
Pricing and availability is not currently available.

Quality Level

200

assay

98%

form

solid

solubility

water: soluble 50 mg/mL, clear

functional group

amine

SMILES string

Cl.CNC(N)=N

InChI

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

InChI key

VJQCNCOGZPSOQZ-UHFFFAOYSA-N

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Application

Methylguanidine hydrochloride can be used to prepare:
  • Biaryl derivatives as BACE1 inhibitors.[1]
  • Modified xylose, which is used in the synthesis of biodegradable composite hydrogels.[2]
  • Methylguanidinium borohydride ionic liquid, which is applicable as a hydrogen storage material.[3]

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKCK6789
MKCQ6942
MKCJ5802
MKCH4785
MKCF9952

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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
Cumming JN, et al.
Bioorganic & Medicinal Chemistry Letters, 22(7), 2444-2449 (2012)
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
Methylguanidinium borohydride: an ionic-liquid-based hydrogen-storage material
Doroodian A, et al.
Angewandte Chemie (International ed. in English), 49(10), 1871-1873 (2010)
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
View All Related Papers

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