Buy Acetone (2-propanone dimethyl ketone) Cas 67-64-1
Buy Acetone (2-propanone dimethyl ketone) Cas 67-64-1
Acetone (2-propanone or dimethyl ketone) is an organic compound with the formula (CH3)2CO.[24] It is the simplest and smallest ketone (R−C(=O)−R’). It is a colorless, highly volatile, and flammable liquid with a characteristic pungent odor.[25]
Acetone is miscible with water and serves as an important organic solvent in industry, home, and laboratory settings. About 6.7 million tonnes were produced worldwide in 2010, mainly for use as a solvent and for production of methyl methacrylate and bisphenol A, which are precursors to widely used plastics.[26][27] It is a common building block in organic chemistry. It serves as a solvent in household products such as nail polish remover and paint thinner. It has volatile organic compound (VOC)-exempt status in the United States.[28]
Acetone is produced and disposed of in the human body through normal metabolic processes. Small quantities of it are present naturally in blood and urine. People with diabetic ketoacidosis produce it in larger amounts. Medical ketogenic diets that increase ketone bodies (acetone, β-hydroxybutyric acid and acetoacetic acid) in the blood are used to suppress epileptic attacks in children with treatment-resistant epilepsy.[29]
Name
From the 17th century, and before modern developments in organic chemistry nomenclature, acetone was given many different names. They included “spirit of Saturn”, which was given when it was thought to be a compound of lead and, later, “pyro-acetic spirit” and “pyro-acetic ester”.[8]
Prior to the name “acetone” being coined by French chemists, it was named “mesit” (from the Greek μεσίτης, meaning mediator) by Carl Reichenbach, who also said that methyl alcohol consisted of mesit and ethyl alcohol.[30][8] Names derived from mesit include mesitylene and mesityl oxide which were first synthesised from acetone. Buy Acetone (2-propanone dimethyl ketone) Cas 67-64-1
In 1839, the name “acetone” began to be used, because it was obtained from acetic acid.[25] Unlike many compounds with the acet- prefix which have a 2-carbon chain, acetone has a 3-carbon chain. That has caused confusion because there can not be a ketone with 2 carbons. The prefix refers to acetone’s relation to vinegar (acetum in Latin, also the source of the words “acid” and “acetic”), rather than its chemical structure.[31]
History
Acetone was first produced by Andreas Libavius in 1606 by distillation of lead(II) acetate.[32][33] In 1832, French chemist Jean-Baptiste Dumas and German chemist Justus von Liebig determined the empirical formula for acetone.[34][35] In 1833, French chemists Antoine Bussy and Michel Chevreul decided to name acetone by adding the suffix -one to the stem of the corresponding acid (viz, acetic acid) just as a similarly prepared product of what was then confused with margaric acid was named margarone.[36][31] By 1852, Alexander William Williamson, an English chemist, realized that acetone was methyl acetyl;[37] the following year, the French chemist Charles Frédéric Gerhardt concurred.[38] In 1865, a German chemist, August Kekulé published the modern structural formula for acetone.[39][40] Johann Josef Loschmidt had presented the structure of acetone in 1861,[41] but his privately published booklet received little attention. During World War I, Chaim Weizmann developed the biochemical process for industrial production of acetone (Weizmann Process).[42]
Production
Acetone is produced directly or indirectly from propene. Approximately 83% of acetone is produced via the cumene process;[27] as a result, acetone production is tied to phenol production. In the cumene process, benzene is alkylated with propylene to produce cumene, which is oxidized by air to produce acetone and phenol:
Lab Grade Acetone | CAS: 67-64-1 | M.F: CH3COCH3 | MW: 58.08, Buy now for reproducible and consistent results from ChemieR at Chemical World.
Acetone is the easiest and the smallest ketone in terms of chemistry and thus it is one of the most used solvents in daily laboratory work. It has a molecular formula of CH3COCH3, and it is made up of three carbon atoms, six hydrogen atoms, and one oxygen atom. Acetone is completely soluble in water and most organic solvents and has the best flexibility in laboratory operations. Acetone Lab Grade is also referred to as 2-propanone or dimethyl ketone and can be used in general laboratory where the performance of the solvent is needed. Buy Acetone (2-propanone dimethyl ketone) Cas 67-64-1
Applications
- Popularly used as an organic solvent in laboratories and research centers.
- Widely used as a rinsing agent of glassware to remove traces prior to final washing.
- Should be used in institutional, academic, and training laboratories.
- Applied in the production of paints and in cleaning the surface.
Key Characteristics
- High Volatility: Dries quickly during cleaning and preparation process.
- Excellent Miscibility: Completely miscible with water and numerous organic solvents.
- Cost-Effective: Economical option of regular laboratory use.
- Flexibility: Usable in reaction, cleaning, as well as sample preparation.
- Stable Results: Favoring daily laboratory activities.
Overview
Acetone Lab Grade (CAS No. 67-64-1, M.F: CH3COCH3, M.W: 58.08), a requisite laboratory solvent, is provided by Chemical World under the ChemieR brand. This grade is designed as a routine laboratory, research and educational grade where high solvency and reliable performance is needed with no strict purity requirements as of ACS grade solvents. It is highly desirable in cleaning glassware, making samples and performing simple chemical reactions due to its high rate of evaporation and ability to dissolve many products.
Chemical World offers this Acetone Lab Grade to guarantee reliable quality and results in the institutional laboratory and research center. It provides competitive prices and reliability in supply of customers who need to know where to purchase Acetone Lab Grade in the United States. This product will present a cost-effective and reliable solution to laboratories that will be compared to the price of the Acetone Lab Grade.
About Brand
ChemieR offers a comprehensive range of ACS grade and ISO 9001:2015 certified products, including high-purity solvents, inorganic reagents, acids, bases, and organic reagents. Our high-quality materials ensure your laboratory achieves precise, reproducible results every time. Rely on ChemieR for trusted, premium-grade chemicals that meet the highest industry standards.
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ue to its high solvency and rapid rate of evaporation, acetone is widely used as a solvent around the world. It is present in various everyday products like adhesives, cleaning fluids, nail polish remover, and paints. Acetone it is a colorless, highly flammable, and volatile liquid that emits a characteristic pungent smell. Acetone is miscible in water and is an essential organic solvent in various industries, homes, and laboratories. It is extensively used in the production of products such as extraction solvents, ink solvents, paint strippers, pharmaceuticals, sealants, and varnishes, to name a few.
IDENTIFIERS
Chemical Name
Acetone (All Grades)
CAS #
67-64-1
EC #
200-662-2
Molecular Formula
C3H6O
InChI Key
CSCPPACGZOOCGX-UHFFFAOYSA-N
Synonyms
Dimethylketone; 2 – Propanone; Acetone; Dimethyl Ketone; DMK
CLASSIFICATIONS
Product Group 1
Solvents
Product Group 2
Construction, Agriculture, Food & Nutrition, HI&I, CASE, Personal Care
PROPERTIES
Acidity (as acetic acid) (Wt %)
Max. 0.002
Appearance
solid or powder form
Benzene (ppm)
Max. 0.5
Color (Pt-Co)
Max. 5
Non-volatile Matter (g/100mL)
Max: 0.002
Permanganate Test (Minutes)
Min: 120
Purity (Wt %)
Min: 99.5
Specific Gravity (20/20° C)
Min: 0.79, Max: 0.793
Water (Wt %)
Min. 99.5
Water Content (Wt %)
Max. 0.5
Water Solubility
solid or powder form
Acetone
- CAS No.
- 67-64-1
- Chemical Name:
- Acetone
- Synonyms
- aceton;propan-2-one;2-Propanone;(CH3)2CO;ACETONE ALCOHOL;Propanon;Dimethylformaldehyde;Propan-1-one;2-Propanon;Dimethylketal
- CBNumber:
- CB3130928
- Molecular Formula:
- C3H6O
- Molecular Weight:
- 58.08
- MOL File:
- 67-64-1.mol
- MSDS File:
- SDS
- Modify Date:
- 8/25/2026 8:17:46 PM
| Melting point | -94 °C(lit.) |
|---|---|
| Boiling point | 56 °C760 mm Hg(lit.) |
| Density | 0.791 g/mL at 25 °C(lit.) |
| vapor density | 2 (vs air) |
| vapor pressure | 184 mm Hg ( 20 °C) |
| refractive index | n20/D 1.359(lit.) |
| FEMA | 3326 | ACETONE |
| Flash point | 1 °F |
| storage temp. | Store at +5°C to +30°C. |
| solubility | Miscible with water and with ethanol (96 per cent). |
| pka | 19.3(at 25℃) |
| form | Liquid |
| Specific Gravity | 0.79 (25/25℃) |
| color | Colorless, invisible vapor |
| Odor | Characteristic pungent odor detectable at 33 to 700 ppm (mean = 130 ppm) |
| PH | 5-6 (395g/l, H2O, 20°C) |
| Relative polarity | 0.355 |
| Odor Threshold | 42ppm |
| biological source | synthetic |
| Odor Type | solvent |
| explosive limit | 2.6-12.8%(V) |
| Water Solubility | soluble |
| Thermal Conductivity | 0.155 W/(m·K) at 25 ℃ |
| λmax | ≤330 nm |
| JECFA Number | 139 |
| Merck | 14,66 |
| BRN | 63580 |
| Henry’s Law Constant | 2.27 at 14.9 °C, 3.03 at 25 °C, 7.69 at 35.1 °C, 11.76 at 44.9 °C (Betterton, 1991) |
| Exposure limits | ACGIH:TLV-TWA 250 ppm (594 mg/m3); TLV-STEL 500 ppm (1187 mg/m3) OSHA:PEL-TWA 1000 ppm (2400 mg/m3) NIOSH:REL-TWA 250 ppm |
| Dielectric constant | 1.0(0℃) |
| Cosmetics Ingredients Functions | DENATURANT SOLVENT FRAGRANCE |
| InChI | 1S/C3H6O/c1-3(2)4/h1-2H3 |
| InChIKey | CSCPPACGZOOCGX-UHFFFAOYSA-N |
| SMILES | CC(C)=O |
| LogP | -0.160 |
| Surface tension | 23.02mN/m at 298.15K |
| Surface tension | 25.2mN/m at 20°C |
| CAS DataBase Reference | 67-64-1(CAS DataBase Reference) |
| NIST Chemistry Reference | Acetone(67-64-1) |
| EPA Substance Registry System | Acetone (67-64-1) |
SAFETY
Risk and Safety Statements
| Symbol(GHS) |   GHS02,GHS07 |
|||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Signal word | Danger | |||||||||
| Hazard statements | H225-H319-H336 | |||||||||
| Precautionary statements | P210-P233-P240-P241-P242-P305+P351+P338 | |||||||||
| target organs | Central nervous system | |||||||||
| Hazard Codes | F,Xi,T | |||||||||
| Risk Statements | 11-36-66-67-39/23/24/25-23/24/25 | |||||||||
| Safety Statements | 9-16-26-45-36/37-7 | |||||||||
| OEB | A | |||||||||
| OEL | TWA: 250 ppm (590 mg/m3) | |||||||||
| RIDADR | UN 1090 3/PG II (ACETONE) | |||||||||
| RIDADR | UN 1091 3/PG II (ACETONE OILS) | |||||||||
| WGK Germany | 3 | |||||||||
| RTECS | AL3150000 | |||||||||
| F | 3-10 | |||||||||
| Autoignition Temperature | 465 °C | |||||||||
| TSCA | TSCA listed | |||||||||
| HazardClass | 3 | |||||||||
| PackingGroup | II | |||||||||
| HS Code | 29141100 | |||||||||
| Storage Class | 3 – Flammable liquids | |||||||||
| Hazard Classifications | Eye Irrit. 2 Flam. Liq. 2 STOT SE 3 |
|||||||||
| Hazardous Substances Data | 67-64-1(Hazardous Substances Data) | |||||||||
| Toxicity | LD50 in rats: 10.7 ml/kg orally (Smyth) | |||||||||
| IDLA | 2,500 ppm | |||||||||
| REACH Registrations | Active | |||||||||
| Limited Quantities | 1.0 L (0.3 gallon) (liquid) | |||||||||
| Excepted Quantities | Max Inner Pack (30g or 30ml) and Max Outer Pack (500g or 500ml) | |||||||||
| Buy Acetone (2-propanone dimethyl ketone) Cas 67-64-1
Buy Acetone (2-propanone dimethyl ketone) Cas 67-64-1 Buy Acetone (2-propanone dimethyl ketone) Cas 67-64-1 Buy Acetone (2-propanone dimethyl ketone) Cas 67-64-1 Buy Acetone (2-propanone dimethyl ketone) Cas 67-64-1 Buy Acetone (2-propanone dimethyl ketone) Cas 67-64-1 Buy Acetone (2-propanone dimethyl ketone) Cas 67-64-1 Buy Acetone (2-propanone dimethyl ketone) Cas 67-64-1 Buy Acetone (2-propanone dimethyl ketone) Cas 67-64-1 |
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Acetone Chemical Properties,Uses,Production
Description
Acetone is a flammable, colorless liquid with a pleasant odor. It is used widely as an organic solvent and in the chemical industry. It is the simplest ketone, which also goes by the name dimethyl ketone (DMK). Acetone was originally referred to as pyroacetic spirit because it was obtained from the destructive distillation of acetates and acetic acid.
Chemical Properties
Acetone, CH3COCH3, also known as 2-propanone and dimethylketone, is a colorless, volatile,flammable liquid that boils at 56°C (133 OF). It is misciblewith water and is oftenused as a solventin the manufacture of lacquers and paints.
Physical properties
Clear, colorless, liquid with a sweet, fragrant odor. Sweetish taste. Odor threshold concentrations ranged from 42 ppmv (Nagata and Takeuchi, 1990) to 100 ppmv (Leonardos et al., 1969). Experimentally determined detection and recognition odor threshold concentrations were 48 mg/m3 (20 ppmv) and 78 mg/m3 (33 ppmv), respectively (Hellman and Small, 1974).
Occurrence
Reported found in apple, pear, grape, pineapple, strawberry, raspberry, tomato, black currant, citrus, onion and potato; also reported found in cocoa leaves, in Mexican goosefoot and in the oils of coriander and lavender. In trace amounts it has been reportedly identified in the oil of bitter orange, in distilled wine and in coffee aroma
History
The traditional method of producing acetone in the 19th century and the beginning of the 20th century was to distill acetates, particularly calcium acetate, Ca(C2H3O2)2.
Weizmann discovered a process to produce butyl alcohol and acetone from the bacterium Clostridium acetobutylicum in 1914. With England’s urgent demand for acetone, Winston Churchill (1874–1965) enlisted Weizmann to develop the Weizmann process for acetone production on an industrial scale. Fermentation and distillation techniques for acetone production were replaced starting in the 1950s with the cumene oxidation process . In this process, cumene is oxidized to cumene hydroperoxide, which is then decomposed using acid to acetone and phenol. This is the primary method used to produce phenol, and acetone is produced as a co-product in the process, with a yield of about 0.6:1 of acetone to phenol.
Uses
Acetone′s luminesence intensity is dependent upon the solution components 1. The absorption of UV light by acetone, results in its photolysis and the production of radials 1.
Definition
ChEBI: A methyl ketone that consists of propane bearing an oxo group at C2.
Production Methods
Acetone is obtained by fermentation as a by-product of n-butyl alcohol manufacture, or by chemical synthesis from isopropyl alcohol; from cumene as a by-product in phenol manufacture; or from propane as a by-product of oxidation-cracking.
General Description
A clear colorless liquid with a sweetish odor. Flash point 0°F. Less dense than water. Vapors are heavier than air. Used as a solvent in paint and nail polish removers.
Air & Water Reactions
Highly flammable. Water soluble.
Reactivity Profile
Acetone was reported that a mixture of Acetone and chloroform, in a residue bottle, exploded. Since addition of Acetone to chloroform in the presence of base will result in a highly exothermic reaction, Acetone is thought that a base was in the bottle [MCA Case History 1661. 1970]. Also, Nitrosyl chloride, sealed in a tube with a residue of Acetone in the presence of platinum catalyst, gave an explosive reaction [Chem. Eng. News 35(43):60. 1967]. The reaction of nitrosyl perchlorate and Acetone ignites and explodes. Explosions occur with mixtures of nitrosyl perchlorate and primary amine [Ann. Chem. 42:2031. 1909]. Reacts violently with nitric acid. Also causes exothermic reaction when in contact with aldehydes.
Health Hazard
The acute toxicity of acetone is low. Acetone is primarily a central nervous system depressant at high concentrations (greater than 12,000 ppm). Unacclimated volunteers exposed to 500 ppm acetone experienced eye and nasal irritation, but it has been reported that 1000 ppm for an 8-hour day produced no effects other than slight transient irritation to eyes, nose, and throat. Therefore there are good warning properties for those unaccustomed to working with acetone; however, frequent use of acetone seems to cause accommodation to its slight irritating properties. Acetone is practically nontoxic by ingestion. A case of a man swallowing 200 mL of acetone resulted in his becoming stuporous after 1 hour and then comatose; he regained consciousness 12 hour later. Acetone is slightly irritating to the skin, and prolonged contact may cause dermatitis. Liquid acetone produces moderate transient eye irritation. Acetone has not been found to be carcinogenic in animal tests or to have effects on reproduction or fertility.
Fire Hazard
HIGHLY FLAMMABLE: Will be easily ignited by heat, sparks or flames. Vapors may form explosive mixtures with air. Vapors may travel to source of ignition and flash back. Most vapors are heavier than air. They will spread along ground and collect in low or confined areas (sewers, basements, tanks). Vapor explosion hazard indoors, outdoors or in sewers. Runoff to sewer may create fire or explosion hazard. Containers may explode when heated. Many liquids are lighter than water.
Flammability and Explosibility
Acetone is extremely flammable (NFPA rating = 3), and its vapor can travel a considerable distance to an ignition source and “flash back.” Acetone vapor forms explosive mixtures with air at concentrations of 2 to 13% (by volume). Carbon dioxide or dry chemical extinguishers should be used for acetone fires.
Pharmaceutical Applications
Acetone is used as a solvent or cosolvent in topical preparations, and as an aid in wet granulation.It has also been used when formulating tablets with water-sensitive active ingredients, or to solvate poorly water-soluble binders in a wet granulation process. Acetone has also been used in the formulation of microspheres to enhance drug release.Owing to its low boiling point, acetone has been used to extract thermolabile substances from crude drugs.
Industrial uses
Acetone is valuable solvent component in acrylic/nitrocellulose automotive lacquers. Acetone is the solvent of choice in film coatings operations which use vinylidene chloride-acrylonitrile copolymer formulations.Other ketones that may be used in these film coating operations include methyl isobutyl ketone, ethyl n-amyl ketone, and diisobutyl ketone.Acetone, blends of MIBK and MEK, methyl namyl ketone, ethyl n-amyl ketone, and diisobutyl ketone are all useful solvents for vinyl resin copolymers. The presence of one of the slower evaporating ketones in the solvent blend prevents quick drying, improves flow, and gives blush resistance to the coating. Acetone is also used as a resin thinner in polyester resins and as a clean up solvent for the resin reactor kettle.In solvents industry, Acetone is a component of solvent blends in urethane, nitrile rubber, and neoprene industrial adhesives.Acetone is the primary solvent in resin-type adhesives and pressure sensitive chlorinated rubber adhesives. Acetone also can be used to extract fats, oils, waxes, and resins from natural products, to dewax lubricating oils, and to extract certain essential oils.Acetone is also an important chemical intermediate in the preparation of several oxygenated solvents including the ketones, diacetone alcohol, mesityl oxide, methyl isobutyl ketone, and isophorone.
Safety
Acetone is considered moderately toxic, and is a skin irritant and severe eye irritant. Skin irritation has been reported due to its defatting action, and prolonged inhalation may result in headaches. Inhalation of acetone can produce systemic effects such as conjunctival irritation, respiratory system effects, nausea, and vomiting.
LD50 (mouse, oral): 3.0 g/kg
LD50 (mouse, IP): 1.297 g/kg
LD50 (rabbit, oral): 5.340 g/kg
LD50 (rabbit, skin): 0.2 g/kg
LD50 (rat, IV): 5.5 g/kg
LD50 (rat, oral): 5.8 g/kg
Potential Exposure
It is used as a solvent in nail polish remover and many other chemicals. Used in the production of lubricating oils and as an intermediate in the manufacture of chloroform and of various pharmaceuticals and pesticides.
Carcinogenicity
Acetone may be weakly genotoxic, but the majority of assays were negative.7 It was not tumorigenic in skin painting studies in mice.
The 2003 ACGIH threshold limit valuetime- weighted average (TLV-TWA) for acetone is 750ppm (1780mg/m3) with a short-term excursion level of 1000ppm (2380mg/m3).
Environmental Fate
Biological. Following a lag time of 20 to 25 h, acetone degraded in activated sludge (30 mg/L) at a rate constant ranging from 0.016 to 0.020/h (Urano and Kato, 1986). Soil bacteria can mineralize acetone to carbon dioxide (Taylor et al., 1980). Bridié et al. (1979) reported BOD and COD values of 1.85 and 1.92 g/g using filtered effluent from a biological sanitary waste treatment plant. These values were determined using a standard dilution method at 20 °C for a period of 5 d. Similarly, Heukelekian and Rand (1955) reported a 5-d BOD value of 0.85 g/g which is 38.5% of the ThOD value of 2.52 g/g. Waggy et al. (1994) reported 5, 15, and 28-d BOD values of 14, 74, and 74%, respectively. Using the BOD technique to measure biodegradation, the mean 5-d BOD value (mM BOD/mM acetone) and ThOD were 1.52 and 38.0%, respectively (Vaishnav et al., 1987).
Photolytic. Photolysis of acetone in air yields carbon monoxide and free radicals, but in isopropanol, pinacol is formed (Calvert and Pitts, 1966). Photolysis of acetone vapor with nitrogen dioxide via a mercury lamp gave peroxyacetyl nitrate as the major product with smaller quantities of methyl nitrate (Warneck and Zerbach, 1992).
Chemical/Physical. Hypochlorite ions, formed by the chlorination of water for disinfection purposes, may react with acetone to form chloroform. This reaction is expected to be significant within the pH range of 6 to 7 (Stevens et al., 1976).
storage
Acetone should be used only in areas free of ignition sources, and quantities greater than 1 liter should be stored in tightly sealed metal containers in areas separate from oxidizers.
Shipping
UN1090 Acetone, Hazard Class: 3; Labels: 3-Flammable liquid
Incompatibilities
Acetone reacts violently with oxidizing agents, chlorinated solvents, and alkali mixtures. It reacts vigorously with sulfur dichloride, potassium t-butoxide, and hexachloromelamine. Acetone should not be used as a solvent for iodine, as it forms a volatile compound that is extremely irritating to the eyes.
Waste Disposal
Consult with environmental regulatory agencies for guidance on acceptable disposal practices. Generators of waste containing this contaminant (≥100 kg/mo) must conform with EPA regulations governing storage, transportation, treatment, and waste disposal. Incineration.
Regulatory Status
Included in the FDA Inactive Ingredients Database (inhalation solution; oral tablets; topical preparations). Included in the Canadian List of Acceptable Non-medicinal Ingredients. Included in nonparenteral medicines licensed in the UK.
Acetone Preparation Products And Raw materials
Raw materials
Preparation Products
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Acetone | 67-64-1 – ChemicalBook
Aug 25, 2026 · Acetone is a flammable, colorless liquid with a pleasant odor. It is used widely as an organic solvent and in the …
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Boiling point: 56 °C760 mm Hg (lit.)
-
Melting point: 94 °C (lit.)
-
Density: 0.791 g/mL at 25 °C (lit.)
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vapor density: 2 (vs air)
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Acetone ACS reagent, = 99.5 67-64-1 – MilliporeSigma
Acetone ACS reagent, ≥99.5%; CAS Number: 67-64-1; EC Number: 200-662-2; Synonyms: 2-propanone,Dimethyl ketone; Linear …
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Acetone Supplier | CAS 67-64-1 | GreenChem Industries
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Acetone (CAS 67-64-1) | Glentham Life Sciences
Buy GK3021 – Acetone (67-64-1) online from Glentham Life Sciences, a manufacturer and supplier of fine chemicals. View catalogue …
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CAS RN: 67-64-1
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Glentham Code: GK3021
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EC Number: 200-662-2
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Acetone Lab Grade | CAS 67-64-1 | High Purity Solvent | Chemical …
Acetone is completely soluble in water and most organic solvents and has the best flexibility in laboratory operations. Acetone Lab …
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Acetone – 2-propanone, Dimethyl ketone – MilliporeSigma
Synonyms: 2-propanone, Dimethyl ketone. CAS 67-64-1. Molecular Weight 58.08. Browse Acetone and related products at …
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Acetone CAS 67-64-1 | 100013 – Merck
Acetone MSDS (material safety data sheet) or SDS, CoA and CoQ, dossiers, brochures and other available documents.
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HOO CHEMTC Acetone Supply | CAS 67-64-1 Industrial Solvent
Acetone, also known as Dimethyl Ketone or Propanone, is a high-purity industrial solvent widely used in coatings, adhesives, …
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Acetone CAS 67-64-1 | 100014 – Merck
EMSURE® grade solvents are suitable for a broad spectrum of classical lab applications, and are frequently used in regulated and …
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CAS RN 67-64-1 | Fisher Scientific
IUPAC Name: propan-2-one. Synonyms: acetone|propanon|dimethylketal|azeton|acetone product|dimethyl formaldehyde|acetone …
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