Ethanol
Ethanol is a volatile, flammable, simple, organic alcohol. Available in various reagent grades, it has applications as a lab/medicinal solvent, an antiseptic, a fuel source/additive, a precursor to organic compounds, etc.
Denatured alcohol (CAS 64-17-5), also known as denatured ethanol or industrial methylated spirit (IMS), is ethanol (ethyl alcohol) to which has been added small known quantities of other substances, so as to ‘denature’ or adulterate it in a controlled manner.
What Additives are Used in Denatured Alcohol?
Often, the additive is methanol (at 5 to 10%), but isopropanol (IPA), methyl ethyl ketone (MEK), acetone or methyl isobutyl ketone (typically all at 1%) may be used. Denatonium can be added for a bitter taste, colored dyes such as methyl violet for visual identification, or a combination may also be used. The purpose of these additives is to create ethanol that is not suitable for human consumption.
The primary purpose of denaturation is to render the ethanol unfit, unpalatable, and unsafe for recreational human consumption, or unsuitable for any other unauthorized purpose. Denaturation usually makes the product exempt from duty payable and other taxes, making it cheaper to purchase.
How Is Denatured Alcohol Used?
Denatured alcohol is used commercially and in industry:
• As a general-purpose solvent, especially for removal of adhesives, waxes, and paint
• For cleaning and degreasing apparatus and equipment
• As a fuel for burners and stoves
• As a surface disinfectant or sterilizer for use in cleanrooms, laboratories, and clinical environments, presented as a liquid, spray, gel, or pre-moistened wiper
• As a preservative and antibacterial agent in cosmetics
Denatured alcohol with added methanol is acutely toxic. It is flammable at room temperature and storage in a secure location is recommended. Due attention should also be given to all other appropriate precautions necessary for handling these chemicals.
Sigma Aldrich Fine Chemicals Biosciences Ethyl alcohol, Pure 200 proof, ACS reagent, >=99.5% | 64-17-5 | MFCD00003568 | 6X1L
Ethyl alcohol, Pure 200 proof, ACS reagent, >=99.5% | Purity: >=99.5% | Mol Wt: 46.07 | 64-17-5 | MFCD00003568 | 6X1L
Sigma Aldrich Fine Chemicals Biosciences Ethyl Alcohol, Pure | 64-17-5 | MFCD00003568 | 4l
Ethyl Alcohol, Pure | Purity: 94% | Mol Wt: 46.07 | 64-17-5 | MFCD00003568 | 4l
Thermo Scientific Production Chemicals and Services GIBCO 20 ETHANOL 200L
NC3840173 GIBCO 20 ETHANOL 200L
Medchemexpress LLC Cintirorgon | 2055536-64-4 | MFCD31544352 | 99.1% | 603.53 g/mol | C27H23F6NO6S | 10 MG
Cintirorgon is a selective, orally bioavailable agonist of the retinoic acid-related orphan receptor gamma (RORγ) developed for research in immuno-oncology. It modulates gene expression in RORγ-expressing T lymphocytes to enhance effector function, reduce immunosuppression, and has shown antitumor activity in preclinical studies.
- Selective RORγ agonist with targeted immunomodulatory activity.
- Orally bioavailable for in vivo pharmacology studies.
- Enhances T cell effector function and reduces immunosuppression.
- High supplied purity, supporting reliable experimental results.
- Characterized molecular profile for reproducible research use.
Medchemexpress LLC Benzeneethanamine, 3,4-dimethoxy-N-methyl-N-[3-[4-[[1-methyl-2-(1-methylethyl)-1H-indol-3-yl]sulfonyl] | 121345-64-0 | 99.8% | 564.74 | 50 MG
SR33805 is a potent Ca2+ channel antagonist with EC50s of 4.1 nM and 33 nM in depolarized and polarized conditions, respectively. It selectively blocks L-type but not T-type Ca2+ channels, making it suitable for research on acute or chronic failing hearts.
- Potent Ca2+ channel antagonist.
- Selectively blocks L-type Ca2+ channels.
- Useful for research on acute or chronic failing hearts.
- Inhibits growth factor-induced proliferation of smooth muscle cells (SMC) in vitro in a dose-dependent manner.
- Restores myocardial infarction (MI)-altered cell shortening without affecting Ca2+ transient amplitude in vitro.
- Improves end-systolic strain and fractional shortening of MI hearts in rats in vivo.
- Significantly reduces intimal hyperplasia in pigs in vivo.
eMolecules m-PEG10-alcohol | 27425-92-9 | MFCD06797087 | 1g
Broadpharm | m-PEG10-alcohol | 1g | 229582257 | BP-22072 | 98.000 | 27425-92-9 | MFCD06797087 | 472.572 | C21H44O11
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Sigma Aldrich Fine Chemicals Biosciences Ethyl alcohol denatured re
The product is denatured ethyl alcohol and it contains following as denaturant1% ethyl acetate 1% hydrocarbons 1% methyl isobutyl ketone 5% methanolEthanol 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. Denatured alcohol is also referred to as industrial methylated spirit.
Medchemexpress LLC Pcc0208017 | 2623158-64-3 | 99.5% | 403.40 | 50 MG
PCC0208017 is a potent microtubule affinity regulating kinases (MARK3/MARK4) inhibitor with IC50s of 1.8 and 2.01 nM, respectively. It suppresses glioma progression both in vitro and in vivo by disrupting microtubule dynamics and inducing G2/M phase cell cycle arrest and cell apoptosis. This compound exhibits robust antitumor activity and good blood-brain barrier (BBB) permeability.
- Inhibits MARK3 and MARK4 activity
- Suppresses glioma progression
- Disrupts microtubule dynamics
- Induces G2/M phase cell cycle arrest and cell apoptosis
- Demonstrates robust antitumor activity in vivo
- Exhibits good BBB permeability
- Decreases Tau phosphorylation
![eMolecules Medchem Express / GNE-0946 / 5mg / 791206460 / HY-19774 / / 1677667-24-1 / [null] / 460.790 / C22H12ClF3N2O4](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502473023.JPG-250.jpg)
eMolecules Medchem Express / GNE-0946 / 5mg / 791206460 / HY-19774 / / 1677667-24-1 / [null] / 460.790 / C22H12ClF3N2O4
Medchem Express / GNE-0946 / 5mg / 791206460 / HY-19774 / / 1677667-24-1 / [null] / 460.790 / C22H12ClF3N2O4
![Medchemexpress LLC 1-(triazolo[1,5-a]pyridin-2-yl)-N-((1S)-1-(2-fluoro-4-(trifluoromethyl)phenyl)ethyl)cyclopropanecarb | 2654741-64-5 | 98.2% | 431.45 g/mol | C22H24F3N5O | 5 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000221514.png-250.jpg)
Medchemexpress LLC 1-(triazolo[1,5-a]pyridin-2-yl)-N-((1S)-1-(2-fluoro-4-(trifluoromethyl)phenyl)ethyl)cyclopropanecarb | 2654741-64-5 | 98.2% | 431.45 g/mol | C22H24F3N5O | 5 MG
SOS1-IN-11 is a small-molecule SOS1 inhibitor for preclinical research. It inhibits SOS1 with an IC50 of 30 nM and is supplied as a light yellow to yellow solid with high purity, suitable for biochemical and cell-based studies.
- Potent SOS1 inhibitor (IC50 30 nM).
- High purity (98.2%).
- Molecular weight 431.45 g/mol.
- Supplied as 5 mg solid for small-scale studies.
- Powder stable at -20°C for up to 3 years.
- Suitable for biochemical and cell-based SOS1 assays.
Medchemexpress LLC Sepimostat (FUT-187 free base) | 103926-64-3 | 98.0% | C21H19N5O2 | 10MG
Sepimostat is a small-molecule NR2B-selective NMDA receptor antagonist reported to exhibit neuroprotective activity by antagonizing the Ifenprodil-binding site. It is supplied as an off-white to yellow solid with reported purity suitable for research and analytical applications.
- Acts as an NR2B-selective NMDA receptor antagonist.
- Exhibits neuroprotective activity in reported studies.
- Inhibits Ifenprodil binding with a reported Ki of 27.7 μM.
- Off-white to yellow solid formulation suitable for analytical use.
- High purity for reproducible experimental results.
- Available in formats suitable for small-scale research workflows.