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Sigma-Aldrich

Ethanol solution

80% v/v, suitable for fixing solution (blood films)

Synonym(s):

Ethanol solution, Ethyl alcohol

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About This Item

Linear Formula:
C2H5OH
CAS Number:
64-17-5
Molecular Weight:
46.07
Beilstein/REAXYS Number:
1718733
MDL number:
MFCD00003568
UNSPSC Code:
15101802
PubChem Substance ID:
24857225
NACRES:
NA.21

product name

Ethanol Fixative 80% v/v, suitable for fixing solution (blood films)

form

liquid
solution

suitability

suitable for fixing solution (blood films)

format

mixture

SMILES string

CCO

InChI

1S/C2H6O/c1-2-3/h3H,2H2,1H3

InChI key

LFQSCWFLJHTTHZ-UHFFFAOYSA-N

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General description

Ethanol Fixative 80% is a solution of 80% v/v ethanol in water. It is used as a preservative for biological specimens in the fluid.

Application

Used as a fixative for blood films in Sigma Procedure 285 for Fetal Hemoglobin

pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Danger

hcodes

H225,H319

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 2

Storage Class

3 - Flammable liquids

wgk_germany

WGK 1

flash_point_f

67.1 °F - closed cup

flash_point_c

19.5 °C - closed cup

Certificates of Analysis (COA)

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The early-time kinetics (<1 s) of lead sulfide (PbS) quantum dot formation are probed using a novel droplet-based microfluidic platform, which allows for high-throughput and real-time optical analysis of the reactive process with millisecond time resolution. The reaction platform enables
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Parkinson's disease (PD) is a common chronic neurodegenerative disorder, usually of idiopathic origin. Symptoms including tremor, bradykinesia, rigidity and postural instability are caused by the progressive loss of dopaminergic neurons in the nigrostriatal region of the brain. Symptomatic therapies are
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The burden of disease due to influenza B is often underestimated. Clinical studies have shown that oseltamivir, a widely used neuraminidase inhibitor (NAI) antiviral drug, may have reduced effectiveness against influenza B viruses. Therefore, it is important to study the
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RNA-guided genome editing with the CRISPR-Cas9 system has great potential for basic and clinical research, but the determinants of targeting specificity and the extent of off-target cleavage remain insufficiently understood. Using chromatin immunoprecipitation and high-throughput sequencing (ChIP-seq), we mapped genome-wide
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