Skip to Content
Merck
All Photos(5)

Key Documents

G4505

Sigma-Aldrich

Guanidine hydrochloride

≥99% (titration), organic base and chaeotropic agent

Synonym(s):

Guanidium Chloride, Aminoformamidine hydrochloride, Aminomethanamidine hydrochloride, Guanidinium chloride

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
NH2C(=NH)NH2 · HCl
CAS Number:
Molecular Weight:
95.53
Beilstein:
3591990
EC Number:
MDL number:
UNSPSC Code:
12352107
PubChem Substance ID:
NACRES:
NA.28

biological source

synthetic (organic)

Quality Level

Assay

≥99% (titration)

form

crystalline powder

technique(s)

RNA extraction: suitable

impurities

≤0.3% water (Karl Fischer)

color

white

pH

(25 °C, 4.6 - 6 at 573 g/L)

mp

180-185 °C (lit.)

solubility

H2O: 6 M

density

1.3 g/cm3 (lit.)

absorption

≤0.10 at 260 nm in H2O at 6 M

SMILES string

Cl[H].NC(N)=N

InChI

1S/CH5N3.ClH/c2-1(3)4;/h(H5,2,3,4);1H

InChI key

PJJJBBJSCAKJQF-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

General description

Guanidine Hydrochloride is a potent protein denaturant extensively utilized in the purification of proteins and nucleic acids. Widely recognized for its versatility, it plays a pivotal role in total RNA extraction experiments, dissolving proteins and disrupting cell structures while inactivating RNA enzymes. Beyond denaturation, Guanidine Hydrochloride is instrumental in renaturing proteins, effectively restoring their active states. It also finds widespread applications in sequencing, molecular weight determinations, and acts as a solubilizing agent for electrophoresis. In summary, Guanidine Hydrochloride stands as a crucial tool in biochemical research, offering indispensable capabilities in the purification, denaturation, and renaturation of proteins and nucleic acids across diverse laboratory applications.

Application

Guanidine hydrochloride (GdnHCl) has been used:
  • to perform absolute quantitation of amyloid-beta (Aß) isoforms in plasma
  • in protein carbonylation assay
  • for the quantification of glycosaminoglycans (GAG)
  • for denaturation of cow′s milk allergens
  • as a control in antiviral screening tests with coxsackievirus B3 (CVB3)
  • in RNA isolation to dissociate nucleoproteins and inhibit RNase
Strong chaotropic agent useful for the denaturation and subsequent refolding of proteins. This strong denaturant can solubilize insoluble or denatured proteins such as inclusion bodies. This can be used as the first step in refolding proteins or enzymes into their active form. Urea and dithiothreitol (DTT) may also be necessary.

Biochem/physiol Actions

Guanidine hydrochloride (GdnHCl) is hydroscopic and a small molecule. It is a potent denaturant of enzymes, which results in conformational changes in the enzyme, leading to complete loss of enzyme activity. GdnHCl is involved in blocking the activity of heat shock protein 104 (Hsp104) adenosine triphosphatase (ATPase) in vivo. It is involved in denaturing alkaline phosphatase (ALPase) in Haliotis diversicolor. GdnHCl leads to the deactivation of enzymes like papain and aminoacylase. GdnHCl, at higher concentrations, is effective in virus inactivation, such as herpes simplex virus 1 (HSV-1).

Features and Benefits

  • Suitable for Biochemical and Cell Biology research
  • Ideal for RNA extraction
  • High purity product for research applications

Packaging

G4505-1KT:
Each kit contains 3 x 100G samples, each sample from a uniquely manufactured lot.

Caution

May agglomerate upon storage. The quality of the product does not appear to be affected and solutions prepared from the free-flowing and lumpy guanidine hydrochloride appear identical. For free-flowing material, please see our Redi-Dri free-flowing product number RDD001.

Preparation Note

In order to make an 8M solution in water, one must heat the solution to 35 °C for approximately 30 minutes.
The maximum solubility of guanidine hydrochloride in water at room temperature is approximately 6M.

Other Notes

For additional information on our range of Biochemicals, please complete this form.

Legal Information

Redi-Dri is a trademark of Sigma-Aldrich Co. LLC

also commonly purchased with this product

related product

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

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

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

T Gebre-Mariam et al.
Journal of ethnopharmacology, 104(1-2), 182-187 (2005-10-20)
Acokanthera schimperi (Apocynaceae), Euclea schimperi (Ebenaceae), Inula confertiflora (Asteraceae), Melilotus elegans (Leguminosae), and Plumbago zeylanica (Plumbaginaceae), are some of the medicinal plants used in Ethiopia for treatment of various skin disorders. In this study, the antiviral activities of the 80%
Melissa A Hausburg et al.
Clinical and experimental rheumatology, 36(5), 891-895 (2018-10-03)
Traumatic joint injury induces chondrocyte dysfunction and progressive breakdown of articular cartilage, leading to post-traumatic osteoarthritis (PTOA). In this condition, dysfunctional fibroblast-like chondrocytes (FLCs) no longer express proteins required for cartilage maintenance, such as SOX9 and collagen-type II (COL2). Interleukin-6
Acetaminophen toxicity up-regulates MRP2 expression in the liver of cats: an old story with new vision
Malekinejad H, et al.
Toxin Reviews, 34, 101-108 (2015)
Vitaliy Ovod et al.
Alzheimer's & dementia : the journal of the Alzheimer's Association, 13(8), 841-849 (2017-07-25)
Cerebrospinal fluid analysis and other measurements of amyloidosis, such as amyloid-binding positron emission tomography studies, are limited by cost and availability. There is a need for a more practical amyloid β (Aβ) biomarker for central nervous system amyloid deposition. We
Current protocols in protein science, 84, A-A (2016-04-03)
The reagents and methods for purification and use of the most commonly used denaturants, guanidine hydrochloride (guanidine-HCl) and urea, are described. Other protein denaturants and reagents used to fold proteins are briefly mentioned. Sulfhydryl reagents (reducing agents) and "oxido-shuffling" (or

Related Content

Find solutions for bulk production, custom packaging, and personalized chemical services to meet your unique research, development, and manufacturing requirements in your industries, including pharmaceuticals, biotechnology, and research institutions.

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service