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Safety Information

A7009

Sigma-Aldrich

Aminoguanidine hemisulfate salt

≥98%

Synonym(s):

Guanylhydrazine hemisulfate salt

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About This Item

Linear Formula:
CH6N4 · 1/2H2SO4
CAS Number:
996-19-0
Molecular Weight:
123.12
EC Number:
213-628-7
MDL number:
MFCD00035665
UNSPSC Code:
12352200
PubChem Substance ID:
24278013
NACRES:
NA.77

biological source

synthetic (organic)

Assay

≥98%

form

powder

solubility

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

storage temp.

room temp

SMILES string

NNC(N)=N.NNC(N)=N.OS(O)(=O)=O

InChI

1S/2CH6N4.H2O4S/c2*2-1(3)5-4;1-5(2,3)4/h2*4H2,(H4,2,3,5);(H2,1,2,3,4)

InChI key

VKGQPUZNCZPZKI-UHFFFAOYSA-N

Gene Information

human ... NOS1(4842) , NOS2(4843) , NOS2B(201288) , NOS2C(645740) , NOS3(4846)

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Application

Aminoguanidine inhibits both constitutive and inducible nitric oxide synthetase. Aminoguanidine has also been used to study the effects of nitric oxide on ovulation and ovarian steroidogenesis and prostaglandin production.

Biochem/physiol Actions

Inhibits both constitutive and inducible nitric oxide synthetase

Features and Benefits

This compound is featured on the Nitric Oxide Synthases page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.

Storage Class Code

13 - Non Combustible Solids

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

A7009-VAR:
A7009-25G:
A7009-BULK:
A7009-100G:

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Certificates of Analysis (COA)

Lot/Batch Number
079K1734V
079K1734
113H0897
093K0039
075H0637

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Caroline Zanotto et al.
Molecular neurobiology, 56(5), 3538-3551 (2018-08-27)
Diabetes mellitus is a metabolic disorder that results in glucotoxicity and the formation of advanced glycated end products (AGEs), which mediate several systemic adverse effects, particularly in the brain tissue. Alterations in glutamatergic neurotransmission and cognitive impairment have been reported
Fernanda Hansen et al.
Amino acids, 48(2), 375-385 (2015-09-09)
Diabetes is a metabolic disease characterized by high fasting-glucose levels. Diabetic complications have been associated with hyperglycemia and high levels of reactive compounds, such as methylglyoxal (MG) and advanced glycation endproducts (AGEs) formation derived from glucose. Diabetic patients have a
Jong Jin Park et al.
Food chemistry, 338, 128150-128150 (2020-10-24)
This study aimed to develop efficient adsorption and desorption processes to purify phenolic compounds from Ecklonia cava. We compared the adsorption and desorption properties of five resins. HP2MG showed the highest adsorption and desorption capacities and adsorption rate; hence, it
Wei Chen et al.
Oxidative medicine and cellular longevity, 2022, 8854457-8854457 (2022-01-18)
Cerebral endothelial cells play an essential role in brain angiogenesis, and their function has been found to be impaired in diabetes. Methylglyoxal (MG) is a highly reactive dicarbonyl metabolite of glucose formed mainly during glycolysis, and its levels can be
J Yamauchi et al.
Endocrinology, 138(9), 3630-3637 (1997-09-01)
Evidence supports the involvement of nitric oxide (NO) in ovarian physiology. The present study was undertaken to investigate the role of the NO/NO synthase (NOS) systems in ovulation, oocyte maturation, ovarian steroidogenesis, and PG production using in vitro perfused rabbit
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