Methyl Blue
CAS No. 28983-56-4
Methyl Blue ( —— )
Catalog No. M24207 CAS No. 28983-56-4
Methyl blue is a triaminotriphenylmethane dye. It is used as an antiseptic dye in the polychrome staining method and has applications in histological and microbiological staining solutions.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
Size | Price / USD | Stock | Quantity |
500MG | 26 | In Stock |
|
1G | Get Quote | In Stock |
|
Biological Information
-
Product NameMethyl Blue
-
NoteResearch use only, not for human use.
-
Brief DescriptionMethyl blue is a triaminotriphenylmethane dye. It is used as an antiseptic dye in the polychrome staining method and has applications in histological and microbiological staining solutions.
-
DescriptionMethyl blue is a triaminotriphenylmethane dye. It is used as an antiseptic dye in the polychrome staining method and has applications in histological and microbiological staining solutions.
-
Synonyms——
-
PathwayOthers
-
TargetOther Targets
-
RecptorOthers
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number28983-56-4
-
Formula Weight799.8
-
Molecular FormulaC37H27N3Na2O9S3
-
Purity>98% (HPLC)
-
SolubilityH2O:19 mg/mL?(23.75mM;?Need ultrasonic)
-
SMILESO=S(C1=CC=CC=C1/N=C2C=C/C(C=C\2)=C(C3=CC=C(NC4=CC=CC=C4S(=O)(O)=O)C=C3)\C5=CC=C(NC6=CC=CC=C6S(=O)([O-])=O)C=C5)([O-])=O.[Na+].[Na+]
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Mohammed Hassan, et al. Micellar effect on the kinetics of oxidation of methyl blue by Ce(IV) in sulfuric acid medium. Arabian Journal of Chemistry. Volume 8, Issue 1, January 2015, Pages 72-77.
molnova catalog
related products
-
PUMA BH3 (TFA)
PUMA BH3 (TFA) is a p53 upregulated modulator of apoptosis (PUMA) BH3 domain peptide, acts as a direct activator of Bak, with a Kd of 26 nM.
-
3-Hydroxybenzylamine
3-Hydroxybenzylamine is a useful organic compound for research related to life sciences.
-
Dehydrodicatechin A
The peroxidase-mediated (+)-catechin oxidation was differentially inhibited by dehydrodicatechin A, showing a competitive type inhibition and a k(I) of 6.4 microM.