Chemodex

Guanidine hydrochloride

CHF 54.00
In stock
CDX-G0040-G100100 gCHF 54.00
CDX-G0040-G500500 gCHF 150.00
More Information
Product Details
Synonyms Aminoformamidine hydrochloride; Aminomethanamidine hydrochloride; Guanidinium chloride; Carbamimidoylazanium chloride
Product Type Chemical
Properties
Formula CH5N3 . HCl
MW 59.07 . 36.46
CAS 50-01-1
RTECS MF4300000
Purity Chemicals ≥99% (Titration)
Appearance White powder.
Solubility Soluble in water (6M) or ethanol (1M).
Identity Determined by 1H-NMR.
Declaration Manufactured by Chemodex.
Other Product Data

Click here for Original Manufacturer Product Datasheet
Our product description may differ slightly from the original manufacturers product datasheet.

InChi Key PJJJBBJSCAKJQF-UHFFFAOYSA-N
Smiles NC([NH3+])=N.[Cl-]
Shipping and Handling
Shipping AMBIENT
Short Term Storage +20°C
Long Term Storage +20°C
Handling Advice Protect from light and moisture.
Use/Stability Stable for at least 2 years after receipt when stored at RT.
Documents
MSDS Download PDF
Product Specification Sheet
Datasheet Download PDF
Description

Guanidine hydrochloride is a powerful, chaotropic agent which is widely used for purification of proteins and nucleic acids. It is useful for denaturation and refolding of proteins as well as in the recovery of periplasmic proteins. At higher concentrations, this strong denaturant has been reported to solubilize denatured insoluble proteins such as inclusion bodies and to increase the solubility of hydrophobic molecules. When utilized at lower concentrations, it is useful in prompting the refolding of denatured proteins. Guanidine hydrochloride is also been reported to allow return of enzymatic activity in protocols using it as a first step. Guanidine hydrochloride is used in RNA isolation to dissociate nucleoproteins and inhibit RNase.

Product References

(1) C. Holm, et al.; Gene 42, 169 (1986) | (2) C.N. Pace, et al.; Biochemistry 29, 2564 (1990) | (3) F.A. Marston, et al.; Meth. Enzymol. 182, 264 (1990) | (4) R. Rudolph & H. Lilie; FASEB J. 10, 49 (1996) | (5) A. Mukhopadhyay; Adv. Biochem. Eng. Biotechnol. 56, 61 (1997) | (6) S. Emadi & M. Behzadi; BBRC 450, 1339 (2014)

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