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Merck

459836

Alcohol etílico puro

greener alternative

≥99.5%, anhydrous, 200 proof

Sinónimos:

Alcohol absoluto, Etanol, etanol no desnaturalizado

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Fórmula lineal:
CH3CH2OH
Número CAS:
64-17-5
Peso molecular:
46.07
UNSPSC Code:
15101802
PubChem Substance ID:
57650645
NACRES:
NA.21
EC Number:
200-578-6
MDL number:
MFCD00003568
Assay:
≥99.5%
Grade:
anhydrous
Bp:
78.3 °C
Vapor pressure:
57.26 hPa ( 19.6 °C)

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Nombre del producto

Alcohol etílico puro, 200 proof, anhydrous, ≥99.5%

SMILES string

OCC

grade

anhydrous

vapor density

1.59 (vs air)

Quality Level

200

vapor pressure

57.26 hPa ( 19.6 °C)

assay

≥99.5%

form

liquid

expl. lim.

3.1-27.7 %

availability

not available in (Sales restictions may apply)

greener alternative product characteristics

Safer Solvents and Auxiliaries
Use of Renewable Feedstocks
Learn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

concentration

200 proof

impurities

<0.005% water

evapn. residue

<0.0005%

color

colorless

pH

7 (20 °C, 10 g/L)

bp

78.3 °C

mp

-114 °C

density

0.789 g/mL at 20 °C

greener alternative category

Aligned,

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General description

Pure ethyl alcohol is a non-denatured 200proof ethanol. Ethanol, a primary alcohol, is an important raw material for the synthesis of various compounds. It can be synthesized either from molasses by fermentation or by hydration of ethylene. It acts as a hydrogen source and reaction medium during the transfer hydrogenation of carbonyl compounds in the presence of sodium hydroxide. The impact of ethanol/water fumigation on the performance of diesel engines has been studied. Anhydrous grade solvents show extremely low percentage water and low residue levels.
We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. Ethanol is environmentally preferable green solvent and thus it aligns with "Safer Solvents and Auxiliaries" and "Use of Renewable Feedstocks". 

Application

Ethanol has been used:
  • as a solvent for lovastatin.
  • as a solvent during the synthesis of (S)-4-hydroxy-2-keto-4-(2′-pyridyl)butyrate.
  • to fix tissue sections on a slide during laser capture microdissection (LCM).

Packaging

View returnable container options.

Other Notes

Pure-Pac® II containers require the Micromatic MacroValve coupler for dispensing solvents, Z560723.
Sales restrictions may apply

Legal Information

Pure-Pac is a registered trademark of Merck KGaA, Darmstadt, Germany

pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Danger

hcodes

H225,H319

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 2

Clase de almacenamiento

3 - Flammable liquids

flash_point_f

55.4 °F - closed cup

flash_point_c

13 °C - closed cup

ppe

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

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Certificados de análisis (COA)

Lot/Batch Number
SHBP1679
SHBC9598V
SHBC9339V
SHBP0166
SHBN8611

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Visite la Librería de documentos

J Harry Sweigard et al.
FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 28(7), 3171-3182 (2014-03-29)
A defining feature in proliferative retinopathies is the formation of pathological neovessels. In these diseases, the balance between neovessel formation and regression determines blindness, making the modulation of neovessel growth highly desirable. The role of the immune system in these
Sukant Khurana et al.
Chemical senses, 38(4), 315-323 (2013-02-01)
We studied complete dose-response curves for 53 odorants in the third instar larvae of Drosophila melanogaster. All odorants, except one, elicited an attraction response. Some odorants also elicited a decrease from their peak response at higher concentrations. This concentration-dependent decrease
Sodium hydroxide-catalyzed transfer hydrogenation of carbonyl compounds and nitroarenes using ethanol or isopropanol as both solvent and hydrogen donor.
Wang D, et al.
J. Mol. Catal. A: Chem., 400, 14-21 (2015)
Assessment of a direct injection diesel engine fumigated with ethanol/water mixtures.
Morsy MH.
Energy Conversion and Management , 94, 406-414 (2015)
Matthew J Walters et al.
Nature protocols, 2(7), 1825-1830 (2007-07-21)
A procedure for the preparation of optically pure alpha-keto-gamma-hydroxy carboxylic acids through stereospecific aldol addition catalyzed by pyruvate aldolases from the Entner-Doudoroff and the DeLey-Doudoroff glycolytic pathways is described. This highly versatile fragment serves as a precursor for a variety
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