Skip to Content
MilliporeSigma
All Photos(2)

Key Documents

362808

Sigma-Aldrich

Reagent Alcohol

≥89% (GC), reagent grade, contains 5% isopropyl alcohol and 5% methyl alcohol as denaturant

Synonym(s):

Denatured ethanol, Ethyl alcohol, Reagent alcohol, Ethanol, RGA, denatured alcohol

Sign Into View Organizational & Contract Pricing


About This Item

CAS Number:
MDL number:
UNSPSC Code:
15101802
PubChem Substance ID:
NACRES:
NA.21

product name

Reagent Alcohol, reagent grade

grade

reagent grade

Quality Level

vapor density

1.59 (vs air)

assay

≥89% (GC)

form

liquid

contains

5% isopropyl alcohol as denaturant
5% methyl alcohol as denaturant

expl. lim.

3.1-27.7 % (lit.)

concentration

100%

impurities

≤0.1% water

evapn. residue

<0.0005%

bp

78 °C (lit.)

mp

-114 °C (lit.)

application(s)

sample preservation

InChI

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

InChI key

LFQSCWFLJHTTHZ-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

General description

Ethanol, also known as Ethyl alcohol, is a primary alcohol. It is a colorless liquid that has low viscosity and is widely used as a solvent and intermediate in organic syntheses. It is miscible in solvents such as water, ketones, ethers, and other alcohols.

Application

Ethanol may be used as solvent in the following application:
  • Solvent in organic synthesis (Ex. Esterification reaction)
  • Solvent for cytofluorimetric analysis
  • Antimicrobial and disinfectant agent
  • Cleaning
  • Purification
  • General Chemical Syntheses

Features and Benefits

Reagent Grade solvents are the perfect choice for very general lab applications. Its specification is defined by assay and offering ≥95% purity.

Components

95 parts of specially denatured ethyl alcohol 3A, 200 proof, with 5 parts of isopropyl alcohol. Final concentrations are ~ 90% ethanol, ~ 5% methanol and ~ 5% isopropanol.

signalword

Danger

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 2 - STOT SE 2

target_organs

Eyes,Central nervous system

Storage Class

3 - Flammable liquids

wgk_germany

WGK 2

flash_point_f

48.2 °F - closed cup

flash_point_c

9 °C - closed cup

ppe

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


Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Lorenzo Di Cesare Mannelli et al.
PloS one, 10(6), e0128080-e0128080 (2015-06-04)
Neurotoxicity is a main side effect of the anticancer drug oxaliplatin. The development of a neuropathic syndrome impairs quality of life and potentially results in chemotherapy dose reductions and/or early discontinuation. In the complex pattern of molecular and morphological alterations
Rocio Gómez-Cansino et al.
Evidence-based complementary and alternative medicine : eCAM, 2015, 183036-183036 (2015-05-20)
The extracts of 14 Julianaceae and 5 Clusiaceae species growing in Mexico were tested in vitro (50 µg/mL) against Mycobacterium tuberculosis H37Rv and HIV reverse transcriptase (HIV-RT). The Julianaceae bark and leaf extracts inhibited M. tuberculosis (>84.67%) and HIV-RT (<49.89%). The
Zeljka Korade et al.
Biological psychiatry, 75(3), 215-222 (2013-07-31)
Smith-Lemli-Opitz syndrome (SLOS) is an inborn error of cholesterol biosynthesis characterized by diminished cholesterol and increased 7-dehydrocholesterol (7-DHC) levels. 7-Dehydrocholesterol is highly reactive, giving rise to biologically active oxysterols. 7-DHC-derived oxysterols were measured in fibroblasts from SLOS patients and an
The uptake of dissolved organic material by the sea cucumber Parastichopus californicus (Stimpson) and its potential role in visceral regeneration.
Brothers CJ, et al.
Journal of Experimental Marine Biology and Ecology, 469, 69-75 (2015)
Miriam Carr et al.
European journal of medicinal chemistry, 45(12), 5752-5766 (2010-10-12)
The synthesis and study of the structure-activity relationships of a series of rigid analogues of combretastatin A-4 are described which contain the 1,4-diaryl-2-azetidinone (β-lactam) ring system in place of the usual ethylene bridge present in the natural combretastatin stilbene products.

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service