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143413

Sigma-Aldrich

1,3-Diaminoguanidine monohydrochloride

98%

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About This Item

Fórmula lineal:
H2NNHC(=NH)NHNH2·HCl
Número de CAS:
36062-19-8
Peso molecular:
125.56
EC Number:
252-854-0
MDL number:
MFCD00012948
UNSPSC Code:
12352100
PubChem Substance ID:
24848585
NACRES:
NA.22

assay

98%

mp

180-182 °C (dec.) (lit.)

solubility

water: soluble 50 mg/mL, clear to very slightly hazy, colorless to faintly yellow

SMILES string

Cl.NNC(=N)NN

InChI

1S/CH7N5.ClH/c2-1(5-3)6-4;/h3-4H2,(H3,2,5,6);1H

InChI key

HAZRIBSLCUYMQP-UHFFFAOYSA-N

General description

1,3-Diaminoguanidine monohydrochloride undergoes condensation reaction with:
  • 4-isothiocyanato-4-methylpentane-2-one to yield condensed pyrimidines
  • various aldehydes and ketones to yield bis guanidine derivatives

Other Notes

Contains sodium chloride

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

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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J Brimnes et al.
APMIS : acta pathologica, microbiologica, et immunologica Scandinavica, 107(6), 555-565 (1999-06-24)
Several N-N-and N-O-containing compounds were analysed for their ability to act as substrates for horseradish peroxidase and peroxidases in Mycobacterium tuberculosis extracts. Aminoguanidine, diaminoguanidine, isoniazid, hydroxylamine and hydrazine were found to be weak substrates for horseradish peroxidase in reaction I
Synthesis of condensed pyrimidines and their evaluation for anti-inflammatory and analgesic activities.
Sondhi SM, et al.
Indian J. Chem. B, 47(1), 136-136 (2008)
Synthesis of biologically active novel bis Schiff bases, bis hydrazone and bis guanidine derivatives.
Sondhi SM, et al.
Indian J. Chem. B, 48(8), 1128-1128 (2009)
Anthony J Lee et al.
Chemical research in toxicology, 18(12), 1927-1933 (2005-12-20)
It is established that aminoguanidine (AG), diaminoguanidine (DAG), and NG-amino-l-arginine (NAA) are metabolism-based inactivators of the three major isoforms of nitric oxide synthase (NOS). In the case of neuronal NOS (nNOS), heme alteration is known to be a major cause
K Kumari et al.
Diabetes, 40(8), 1079-1084 (1991-08-01)
Mono- and diaminoguanidine inhibited ambient glucose-induced glycosylated end product formation of albumin and collagen 125I-labeled albumin covalent binding in vitro. Diaminoguanidine was a stronger inhibitor than monoaminoguanidine. These compounds also inhibited rat eye lens aldose reductase activity in vitro noncompetitively
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