362808
Reagent Alcohol
≥89% (GC), reagent grade, contains 5% isopropyl alcohol and 5% methyl alcohol as denaturant
Sign Into View Organizational & Contract Pricing
All Photos(2)
Synonym(s):
Denatured ethanol, Ethyl alcohol, Reagent alcohol, Ethanol, RGA, denatured alcohol
CAS Number:
MDL number:
UNSPSC Code:
15101802
PubChem Substance ID:
NACRES:
NA.21
Recommended Products
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
Related Categories
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.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Flam. Liq. 2 - STOT SE 2
Target Organs
Eyes,Central nervous system
WGK
WGK 2
Flash Point(F)
closed cup
Flash Point(C)
closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
危险化学品
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
Already Own This Product?
Find documentation for the products that you have recently purchased in 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
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)
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
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