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Merck

1808

Methylene Blue Solution 1.4%(w/v)95%ethanol | 7220-79-3

1.4 % (w/v) in 95% ethanol

Synonym(s):

Methylene Blue solution, Ehrlich’s reagent III, Loeffler’s Methylene Blue

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About This Item

Empirical Formula (Hill Notation):
C16H18ClN3S
CAS Number:
Molecular Weight:
319.85
UNSPSC Code:
12171500
NACRES:
NA.47
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
3641570

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Product Name

Methylene Blue Solution 1.4%(w/v)95%ethanol | 7220-79-3, 1.4 % (w/v) in 95% ethanol

InChI key

CXKWCBBOMKCUKX-UHFFFAOYSA-M

InChI

1S/C16H18N3S.ClH/c1-18(2)11-5-7-13-15(9-11)20-16-10-12(19(3)4)6-8-14(16)17-13;/h5-10H,1-4H3;1H/q+1;/p-1

SMILES string

[Cl-].CN(C)c1ccc2N=C3C=C\C(C=C3Sc2c1)=[N+](/C)C

form

solution

IVD

for in vitro diagnostic use

concentration

1.4 % (w/v) in 95% ethanol

storage temp.

15-25°C

Quality Level

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1 of 4

This Item
504840397877515
concentration

1.4 % (w/v) in 95% ethanol

concentration

0.5% in H2O (0.5 g/100 mL)

concentration

1.5% (1.5 g/ 100 mL)

concentration

-

form

solution

form

-

form

liquid

form

solution

IVD

for in vitro diagnostic use

IVD

-

IVD

-

IVD

-

Quality Level

500

Quality Level

-

Quality Level

100

Quality Level

-

storage temp.

15-25°C

storage temp.

-

storage temp.

room temp

storage temp.

-

Application

Used as a nuclear counterstain in the various Lymphocyte Enzyme kits, Procedure No. 181

pictograms

FlameExclamation mark

signalword

Danger

hcodes

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 2

Storage Class

3 - Flammable liquids

wgk

WGK 2

flash_point_f

55.4 °F

flash_point_c

13 °C

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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The first gold-mercaptopropionic acid-polyethylenimine composite based electrochemical DNA biosensor was fabricated for the early detection of Streptococcus pyogenes infection in humans causing rheumatic heart disease (heart valve damage). No biosensor is available for the detection of rheumatic heart disease (RHD).
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N6-methyladenosine (m6A) on mRNAs is critical for various biological processes, yet whether m6A regulates drug resistance remains unknown. Here we show that developing resistant phenotypes during tyrosine kinase inhibitor (TKI) therapy depends on m6A reduction resulting from FTO overexpression in
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The genome of the rice blast fungus Magnaporthe oryzae codes for two proteins with N-terminal dioxygenase (DOX) and C-terminal cytochrome P450 (CYP) domains, respectively. One of them, MGG_13239, was confirmed as 7,8-linoleate diol synthase by prokaryotic expression. The other recombinant

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