PRODUCTS

METHYL AMYL KETONE

Methyl amyl ketone is a colorless liquid with a strong, sweet odor.
Methyl amyl ketone is a member of the ketone family of organic compounds and has a molecular formula of C6H12O.
Methyl amyl ketone is commonly used as a solvent in various industrial applications due to Methyl amyl ketone unique properties and advantages.

CAS Number: 110-43-0
EC Number: 203-767-1
Molecular Dormula: C7H14O
Molar Weight: 114.185

Methyl amyl ketone, also known as Methyl amyl ketone, or Heptan-2-one, is a ketone with the molecular formula C7H14O.
Methyl amyl ketone is a colorless, water-like liquid with a banana-like, fruity odor.
Methyl amyl ketone has a neutral formal charge, and is only slightly soluble in water.

Methyl amyl ketone is a natural product found in Aloe africana, Zingiber mioga, and other organisms with data available.
Methyl amyl ketone is a metabolite found in or produced by Saccharomyces cerevisiae.

Methyl amyl ketone is registered under the REACH Regulation and is manufactured in and / or imported to the European Economic Area, at ≥ 100 to < 1 000 tonnes per annum.
Methyl amyl ketone is used by consumers, by professional workers (widespread uses), in formulation or re-packing and at industrial sites.

Methyl amyl ketone is listed by the FDA as a "food additive permitted for direct addition to food for human consumption" (21 CFR 172.515), and Methyl amyl ketone occurs naturally in certain foods (e.g., beer, white bread, butter, various cheeses and potato chips).

The mechanism of action of Methyl amyl ketone as a pheromone at odorant receptors in rodents has been investigated.
Methyl amyl ketone is present in the urine of stressed rats and believe that Methyl amyl ketone is used as a means to alert other rats.

Certain species of worms are attracted to Methyl amyl ketone and bacteria can use this as a means of pathogenesis.
Methyl amyl ketone has also been found to be excreted by honey bees when they bite small pests within the colony such as wax moth larvae and Varroa mites.

Though Methyl amyl ketone was historically believed to be an alarm pheromone, Methyl amyl ketone has been shown to act as an anaesthetic on the pests, enabling the honey bee to stun the pest and eject Methyl amyl ketone from the hive.
The work could lead to the use of Methyl amyl ketone as an alternative local anaesthetic to lidocaine, which although well established for clinical use, has the disadvantage of provoking allergic reactions in some people.

Methyl amyl ketone was one of the metabolites of n-heptane found in the urine of employees exposed to heptane in shoe and tire factories.
This commonly occurs from exposure to plasticisers.

Methyl amyl ketone can be absorbed through the skin, inhaled and consumed.
Exposure to Methyl amyl ketone can cause irritation of skin/eyes, respiratory system, headaches, vomiting, and nausea.

In mice 2-H is a urinary component and pheromone.
Methyl amyl ketone has a high affinity for the main olfactory epithelium.
Gaillard et al 2002 found that Methyl amyl ketone agonizes one specific olfactory receptor, and that that OR only binds 2-H.

One of the key advantages of Methyl amyl ketone is its high solvency power.
Methyl amyl ketone is a very effective solvent for many organic compounds, particularly those that are insoluble in water.

This makes Methyl amyl ketone useful in applications such as paint and coating formulations, adhesives, and inks.
Methyl amyl ketone is also used as a solvent in the production of various chemicals, such as pharmaceuticals and pesticides.

Another advantage of Methyl amyl ketone is Methyl amyl ketone relatively low toxicity compared to other ketones.
Methyl amyl ketone has a lower vapor pressure and boiling point than other ketones, which means that Methyl amyl ketone is less likely to vaporize and become a hazard in the workplace.

However, Methyl amyl ketone is still important to handle Methyl amyl ketone with care and use Methyl amyl ketone in accordance with appropriate safety protocols.
This includes the use of protective equipment, such as gloves and safety goggles, as well as proper ventilation and storage.

Methyl amyl ketone is also used in the production of fragrances and flavors, as well as in the production of resins and polymers.
Methyl amyl ketone is a useful intermediate in the production of other chemicals and is used as a starting material in the production of other ketones.
Methyl amyl ketone is also used as a fuel additive to improve the combustion efficiency of gasoline.

Methyl amyl ketone has a high solvent activity, slow evaporation rate, low density, low surface tension, and high boiling point.
These properties make Methyl amyl ketone a very good solvent for cellulosic lacquers, acrylic lacquers, and high-solids coatings.
Because regulations limit the weight of solvent per gallon of coating, formulators favor the use of low-density solvents that help reduce the VOC content of a coating.

Methyl amyl ketone is lower in density than ester, aromatic hydrocarbons, and glycol ether solvents with similar evaporation rates.
The low density and high activity of Methyl amyl ketone are significant advantages when formulating high-solids coatings to meet VOC guidelines.
Methyl amyl ketone is also used as a polymerization solvent for high solids acrylic resins.

The chemical substances for Methyl amyl ketone are listed as Inert Ingredients Permitted for Use in Nonfood Use Pesticide Products, and in Food Use Pesticide Products with limitations, under the Federal Insecticide, Fungicide, and Rodenticide Act (FIFRA).

Applications of Methyl amyl ketone:
Auto OEM
Auto refinish
General industrial coatings
Herbicides int
Paints & coatings
Process solvents

Uses of Methyl amyl ketone:
Methyl amyl ketone is used for the synthesis of industrial solvents and fragrances, such as the components used to make caryophyllum oil.

Micro-amounts are suitable for carnation or other octyl fragrance types, which can be shared with Artemisia or basil, seashell oil in herb fragrance types, the formation of a new head fragrance.
With the spice, fruit flavor can coordinate and good synthesis.

In the food flavor, for the banana type food flavor can increase the milk fat flavor, also suitable for coconut, cream, cheese flavor food flavor.
GB 2760-96 provides for the permitted use of flavorants.

Methyl amyl ketone is mainly used in the preparation of cheese, banana, cream and coconut flavor.
Methyl amyl ketone is used for the synthesis of industrial solvents and fragrances, such as the components used to make caryophyllum oil.

Methyl amyl ketone is widely used in industrial solvent, fiber, medicine, pesticide, perfume chemical industry and other fields
Methyl amyl ketone is used in organic synthesis; Trace suitable for carnation or other octanoaromatic type, in the herb fragrance can be shared with the grass Artemisia or basil, Sea oil, the formation of new head fragrance.

With the spice, fruit flavor can coordinate and good synthesis.
In the food flavor, for the banana type food flavor can increase the milk fat flavor, also suitable for coconut, cream, cheese flavor food flavor; For industrial solvents, fiber, medicine, pesticide, perfume and Chemical Industry.

Methyl amyl ketone is used as a solvent for resins and lacquers, a fragrance for cosmetics, and a flavor for foods.
Methyl amyl ketone is solvent for nitrocellulose lacquers.

Methyl amyl ketone is used in perfumery as constituent of artificial carnation oils; as industrial solvent
Methyl amyl ketone is used as a solvent in metal roll coatings and in synthetic resin finishes and lacquers, as a flavoring agent, and in perfumes.

Methyl amyl ketone can be used in the following industries:
Food & Feed, Pharma & Life Science, Other Industries, Cosmetics & Personal Care

Methyl amyl ketone can be applied as:
Oleochemicals, Fragrances, Food Additives

Consumer Uses:
Methyl amyl ketone is used in the following products: plant protection products, adhesives and sealants, coating products, fillers, putties, plasters, modelling clay, cosmetics and personal care products, air care products, biocides (e.g. disinfectants, pest control products), perfumes and fragrances, polishes and waxes and washing & cleaning products.
Other release to the environment of Methyl amyl ketone is likely to occur from: indoor use as processing aid and outdoor use as processing aid.

Other Consumer Uses:
Binder
Paint additives and coating additives not described by other categories
Solvent
Solvents (which become part of product formulation or mixture)

Widespread uses by professional workers:
Methyl amyl ketone is used in the following products: washing & cleaning products, fertilisers, plant protection products, coating products, cosmetics and personal care products, polishes and waxes, laboratory chemicals and polymers.
Methyl amyl ketone is used in the following areas: agriculture, forestry and fishing.

Methyl amyl ketone is used for the manufacture of: machinery and vehicles.
Other release to the environment of Methyl amyl ketone is likely to occur from: indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners) and outdoor use.

Uses at industrial sites:
Methyl amyl ketone is used in the following products: coating products, photo-chemicals, laboratory chemicals and semiconductors.
Methyl amyl ketone is used in the following areas: scientific research and development.

Methyl amyl ketone is used for the manufacture of: machinery and vehicles, chemicals and electrical, electronic and optical equipment.
Release to the environment of Methyl amyl ketone can occur from industrial use: in processing aids at industrial sites, in the production of articles, as an intermediate step in further manufacturing of another substance (use of intermediates) and as processing aid.

Industry Uses:
Cleaning agent
Intermediates
Paint additives and coating additives not described by other categories
Solvent
Solvents (which become part of product formulation or mixture)

Industrial Processes with risk of exposure:
Painting (Solvents)
Plastic Composites Manufacturing

Key attributes of Methyl amyl ketone:
Excellent solvent activity
High dilution ratio
Inert - Food use with limitations
Inert - Nonfood use
Low density
Low surface tension
Non-HAP
Non-SARA
REACH compliant
Readily Biodegradable
Slow evaporation rate
Urethane grade

Nature of Methyl amyl ketone:
Methyl amyl ketone is colorless, fragrant, stable liquid.
Methyl amyl ketone is slightly soluble in water.

Methyl amyl ketone is melting Point -35 °c.
Methyl amyl ketone is boiling point 151.5 °c.

Methyl amyl ketone is relative density 0.8166.
Methyl amyl ketone is refractive index 4067.

Methyl amyl ketone is viscosity (25 °c) 0.766MPA.
Methyl amyl ketone is flash point 47.
Methyl amyl ketone is very slightly soluble in water, soluble in ethanol, ether.

Preparation Method of Methyl amyl ketone:
The extraction method is obtained by extracting clove oil or cinnamon oil.
2-heptanol method is prepared by dehydrogenation of 2-heptanol.
n-butyl acetoacetate method.

Production Method of Methyl amyl ketone:
1. Obtained by saponification of ethyl butyl acetoacetate.
Ethyl butyl acetoacetate was added to 5% sodium hydroxide solution and stirred at room temperature for 4H.

The layers were allowed to stand and separated.
The aqueous layer reacts with 50% sulfuric acid, and as the reaction becomes moderate to the release of carbon dioxide, the reaction is slowly heated to boil, distilling from 0.33 to 0.5% of the original total volume.

The distillate was made alkaline with solid sodium hydroxide and then distilled off 80-90%.
The distillate is layered, the ketone is separated into layers, and the water layer is distilled out for one third.

After the ketone is removed from the distilled material, the water layer is further distilled out for one third, which is repeated in this way, the resulting Methyl amyl ketone was collected as far as possible.
The resulting Methyl amyl ketone was combined and washed with calcium chloride solution.
After drying, Methyl amyl ketone was obtained by distillation with a yield of 50-60%.

2. The extraction method is obtained by extracting clove oil or cinnamon oil.

3. 2-heptanol method from 2-heptanol dehydrogenation.
At room temperature with sodium hydroxide saponification of butyl acetyl ethyl acetate, then add sulfuric acid, heating distillation, distillate with sodium hydroxide neutralization, distillation, plus calcium chloride concentrated solution to remove residual ethanol, after drying and distillation.

Manufacturing Methods of Methyl amyl ketone:
Produced industrially by reductive condensation of acetone with butyraldehyde in one or two steps.

General Manufacturing Information of Methyl amyl ketone:

Industry Processing Sectors:
All Other Basic Organic Chemical Manufacturing
Computer and Electronic Product Manufacturing
Construction
Furniture and Related Product Manufacturing
Miscellaneous Manufacturing
Non-metallic Mineral Product Manufacturing (includes clay, glass, cement, concrete, lime, gypsum, and other non-metallic mineral product manufacturing)
Not Known or Reasonably Ascertainable
Paint and Coating Manufacturing
Transportation Equipment Manufacturing

Handling and Storage of Methyl amyl ketone:

Nonfire Spill Response:
ELIMINATE all ignition sources (no smoking, flares, sparks or flames) from immediate area.
All equipment used when handling Methyl amyl ketone must be grounded.

Do not touch or walk through spilled material.
Stop leak if you can do Methyl amyl ketone without risk.

Prevent entry into waterways, sewers, basements or confined areas.
A vapor-suppressing foam may be used to reduce vapors.

Absorb or cover with dry earth, sand or other non-combustible material and transfer to containers.
Use clean, non-sparking tools to collect absorbed material.

LARGE SPILL:
Dike far ahead of liquid spill for later disposal.
Water spray may reduce vapor, but may not prevent ignition in closed spaces.

Storage of Methyl amyl ketone:
Keep in tightly closed container in a cool and dry place, protected from light.
When stored for more than 24 months, quality should be checked before use.
We believe the above information to be correct but we do not present Methyl amyl ketone as all inclusive and as such should be used as a guide.

Chemical Reactivity of Methyl amyl ketone:

Reactivity Profile:
Methyl amyl ketone reacts exothermically with many acids and bases to produce flammable gases (e.g., H2).
The heat may be sufficient to start a fire in the unreacted portion.

Reacts with reducing agents such as hydrides, alkali metals, and nitrides to produce flammable gas and heat.
Incompatible with isocyanates, aldehydes, cyanides, peroxides, and anhydrides.

Incompatible with many oxidizing agents including nitric acid, nitric acid/hydrogen peroxide mixture, and perchloric acid.
May form peroxides.

Reactivity with Water:
No reaction

Reactivity with Common Materials:
Will attack some forms of plastic.

Stability During Transport:
Stable

Neutralizing Agents for Acids and Caustics:
Not pertinent

Polymerization:
Not pertinent

Inhibitor of Polymerization:
Not pertinent

First Aid Measures of Methyl amyl ketone:

Eye:
IRRIGATE IMMEDIATELY - If this chemical contacts the eyes, immediately wash (irrigate) the eyes with large amounts of water, occasionally lifting the lower and upper lids.
Get medical attention immediately.

Skin:
SOAP WASH - If this chemical contacts the skin, wash the contaminated skin with soap and water.

Breathing:
FRESH AIR - If a person breathes large amounts of this chemical, move the exposed person to fresh air at once.
Other measures are usually unnecessary.

Swallow:
MEDICAL ATTENTION IMMEDIATELY - If this chemical has been swallowed, get medical attention immediately.

Fire Fighting of Methyl amyl ketone:
The majority of these products have a very low flash point.
Use of water spray when fighting fire may be inefficient.

For fire involving UN1170, UN1987 or UN3475, alcohol-resistant foam should be used.
Ethanol (UN1170) can burn with an invisible flame.
Use an alternate method of detection (thermal camera, broom handle, etc.).

SMALL FIRE:
Dry chemical, CO2, water spray or alcohol-resistant foam.

LARGE FIRE:
Water spray, fog or alcohol-resistant foam.
Avoid aiming straight or solid streams directly onto Methyl amyl ketone.
If it can be done safely, move undamaged containers away from the area around the fire.

FIRE INVOLVING TANKS OR CAR/TRAILER LOADS:
Fight fire from maximum distance or use unmanned master stream devices or monitor nozzles.
Cool containers with flooding quantities of water until well after fire is out.

Withdraw immediately in case of rising sound from venting safety devices or discoloration of tank.
ALWAYS stay away from tanks engulfed in fire.

For massive fire, use unmanned master stream devices or monitor nozzles.
If this is impossible, withdraw from area and let fire burn.

Fire Hazards of Methyl amyl ketone:

Flash Point:
117°F O.C. 102°F C.C.

Flammable Limits in Air: 1.11%-7.9%

Fire Extinguishing Agents:
Dry chemical, alcohol foam, carbon dioxide

Fire Extinguishing Agents Not to Be Used:
Water may be ineffective.

Special Hazards of Combustion Products:
Currently not available

Behavior in Fire:
Currently not available

Auto Ignition Temperature:
740°F

Spillage Disposal of Methyl amyl ketone:

Personal protection:
Filter respirator for organic gases and vapours adapted to the airborne concentration of Methyl amyl ketone.
Collect leaking and spilled liquid in sealable metal containers as far as possible.

Absorb remaining liquid in dry sand or inert absorbent.
Then store and dispose of according to local regulations. Do NOT wash away into sewer.

Identifiers of Methyl amyl ketone:
CAS Number: 110-43-0
ChEBI: CHEBI:5672
ChEMBL: ChEMBL18893
ChemSpider: 7760
ECHA InfoCard: 100.003.426
KEGG: C08380
PubChem CID: 8051
UNII: 89VVP1B008
CompTox Dashboard (EPA): DTXSID5021916
InChI: InChI=1S/C7H14O/c1-3-4-5-6-7(2)8/h3-6H2,1-2H3
Key: CATSNJVOTSVZJV-UHFFFAOYSA-N
InChI=1/C7H14O/c1-3-4-5-6-7(2)8/h3-6H2,1-2H3
Key: CATSNJVOTSVZJV-UHFFFAOYAO
SMILES: O=C(C)CCCCC

Substance: Methyl amyl ketone
CAS: 110-43-0
EC number: 203-767-1
REACH compliant: Yes
Min. purity / concentration: 100%
Appearance: Liquid
Grades: Cosmetic, Pharma, Technical

IUPAC name: Methyl amyl ketone
Molecular formula: C7H14O
Molar Weight [g/mol]: 114.185

EC / List no.: 203-767-1
CAS no.: 110-43-0
Mol. formula: C7H14O

Synonyms: Methyl pentyl ketone, Methyl amyl ketone
Linear Formula: CH3(CH2)4COCH3
CAS Number: 110-43-0
Molecular Weight: 114.19
EC Number: 203-767-1

Properties of Methyl amyl ketone:
Chemical formula: C7H14O
Molar mass: 114.18 g/mol
Appearance: Clear liquid
Odor: banana-like, fruity
Density: 0.8 g/mL
Melting point: −35.5 °C (−31.9 °F; 237.7 K)
Boiling point: 151 °C (304 °F; 424 K)
Solubility in water: 0.4% by wt
Vapor pressure: 3 mmHg (20°C)
Magnetic susceptibility (χ): -80.50·10−6 cm3/mol

Appearance: colorless clear liquid (est)
Assay: 95.00 to 100.00
Food Chemicals Codex Listed: Yes
Specific Gravity: 0.81400 to 0.81900 @ 25.00 °C.
Pounds per Gallon - (est).: 6.773 to 6.815
Refractive Index: 1.40800 to 1.41500 @ 20.00 °C.
Melting Point: -26.90 °C. @ 760.00 mm Hg
Boiling Point: 149.00 to 150.00 °C. @ 760.00 mm Hg
Boiling Point: 151.00 °C. @ 2.60 mm Hg
Acid Value: 2.00 max. KOH/g
Vapor Pressure: 4.732000 mmHg @ 25.00 °C. (est)
Flash Point: 117.00 °F. TCC ( 47.22 °C. )
logP (o/w): 1.980

Formula: C7H14O / CH3(CH2)4COCH3
Molecular mass: 114.18
Boiling point: 151°C
Melting point: -35.5°C
Relative density (water = 1): 0.8
Solubility in water: poor
Vapour pressure, kPa at 25°C: 0.2
Relative vapour density (air = 1): 3.9
Relative density of the vapour/air-mixture at 20°C (air = 1): 1.01
Flash point: 39°C
Auto-ignition temperature: 393°C
Explosive limits, vol% in air: 1-5.5

Molecular Weight: 114.19
XLogP3: 2
Hydrogen Bond Donor Count: 0
Hydrogen Bond Acceptor Count: 1
Rotatable Bond Count: 4
Exact Mass: 114.104465066
Monoisotopic Mass: 114.104465066
Topological Polar Surface Area: 17.1 Å²
Heavy Atom Count: 8
Complexity: 66.8
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes

Related Products of Methyl amyl ketone:
Nivalenol
(R)-Ochratoxin α
Di-N-heptytin Dichloride-D30
Ergosinine
3-Ethyl-2-methylpentane

Alternate Chemical Names:
BUTYLACETONE
2-HEPTANONE
2-KETOHEPTANE
METHYL (N-AMYL) KETONE
METHYL AMYL KETONE
METHYL N-AMYL KETONE
METHYL N-PENTYL KETONE
METHYL PENTYL KETONE
METHYLAMYL KETONE
1-METHYLHEXANAL
N-AMYL METHYL KETONE
N-PENTYL METHYL KETONE
2-OXOHEPTANE
PENTYL METHYL KETONE

Names of Methyl amyl ketone:

Regulatory process names:
2-Heptanone
2-Heptanone (natural)
Amyl methyl ketone
Amyl-methyl-cetone
Butylacetone
Heptan-2-one
Heptan-2-one
heptan-2-one
heptan-2-one; methyl amyl ketone
Ketone C-7
Ketone, methyl pentyl
Methyl amyl ketone
methyl amyl ketone
Methyl n-amyl ketone
Methyl n-pentyl ketone
Methyl pentyl ketone
Methyl-amyl-cetone
n-AMYL METHYL KETONE
n-Amyl methyl ketone
n-Pentyl methyl ketone
Pentyl methyl ketone

Translated names:
2-heptanon (no)
2-heptanon (sv)
2-heptanonas (lt)
2-heptanoni (fi)
eptan-2-one (it)
heptaan-2-on (nl)
Heptaan-2-oon (et)
heptan-2-on (cs)
heptan-2-on (da)
Heptan-2-on (de)
heptan-2-on (hr)
heptan-2-on (no)
heptan-2-on (pl)
heptan-2-on (sl)
heptan-2-on (sv)
heptan-2-ona (es)
heptan-2-ona (ro)
heptan-2-one; méthylamylcétone (fr)
heptan-2-oni (fi)
heptano-2-ona (pt)
heptanons-2 (lv)
heptán-2-on (hu)
heptán-2-ón (sk)
keton metylowo-n-amylowy (pl)
keton metylowo-pentylowy (pl)
methyl(pentyl)keton (cs)
methylpentylketon (da)
Methylpentylketon (de)
metil amil chetone (it)
metil amil keton (sl)
metil amil ketona (ro)
metil-amil-keton (hr)
metil-amil-keton (hu)
metilamilketonas (lt)
metilamilketons (lv)
metyl(pentyl)ketón (sk)
metyloamyloketon (pl)
metylpentylketon (no)
metylpentylketon (sv)
metyyliamyyliketoni (fi)
Metüülamüülketoon (et)
méthyl-n-amylcétone (fr)
επταν-2-όν (el)
метил амил кетон (bg)
хептан-2-oн (bg)

CAS name:
2-Heptanone

IUPAC names:
2-HEPTANONE
2-Heptanone
2-heptanone
2-Heptanoneheptane-2-onheptane-2-oneheptane-2-one methyl amyl ketoneMETHYL AMYL KETONEMethyl N Amyl KetoneMETHYL N-AMYL KETONEMethyl N.A Ketone (2-heptanone)
heptan-2-on
Heptan-2-one
heptan-2-one
Heptan-2-one
heptan-2-one
heptan-2-one methyl amyl ketone
METHYL AMYL KETONE
Methyl Amyl Ketone
Methyl amyl ketone
methyl amyl ketone
Methyl N Amyl Ketone
METHYL N-AMYL KETONE
Methyl N.A Ketone (2-Heptanone)

Preferred IUPAC name:
Heptan-2-one

Trade names:
EH2350PTA-1128(M)
EH2350PTA-2260(M)
EH2350PTA-RAL9002(M)
MAK

Other names:
Amyl methyl ketone
Butyl acetone
Methyl n-amyl ketone
Methyl pentyl ketone

Other identifiers:
110-43-0
606-024-00-3

Synonyms of Methyl amyl ketone:
2-HEPTANONE
Heptan-2-one
110-43-0
Methyl pentyl ketone
Butylacetone
Amyl methyl ketone
Methyl amyl ketone
Methyl n-amyl ketone
n-Amyl methyl ketone
n-Pentyl methyl ketone
Heptanone
Pentyl methyl ketone
Methyl n-pentyl ketone
Ketone, methyl pentyl
Amyl-methyl-cetone
Methyl-amyl-cetone
Ketone C-7
FEMA No. 2544
NSC 7313
CHEMBL18893
CHEBI:5672
DTXSID5021916
89VVP1B008
NSC-7313
Methyl-n-amylketone
DTXCID601916
2-Heptanone (natural)
FEMA Number 2544
Amyl-methyl-cetone [French]
Methyl-amyl-cetone [French]
CAS-110-43-0
HSDB 1122
EINECS 203-767-1
UN1110
BRN 1699063
UNII-89VVP1B008
AI3-01230
CCRIS 8809
1-Methylhexanal
2-Ketoheptane
heptanone-2
methylpentylketone
2-heptanal
2-Oxoheptane
Nat. 2-Heptanone
2-Heptanone, 98%
2-Heptanone, 99%
2-HEPTANONE [MI]
EC 203-767-1
n-C5H11COCH3
2-HEPTANONE [FCC]
2-HEPTANONE [FHFI]
2-HEPTANONE [HSDB]
SCHEMBL29364
4-01-00-03318 (Beilstein Handbook Reference)
2-heptanone_GurudeebanSatyavani
SCHEMBL1122991
WLN: 5V1
2-Heptanone, analytical standard
2-Heptanone(Methyl Amyl Ketone)
NSC7313
2-Heptanone, natural, 98%, FG
Methyl n-Amyl Ketone Reagent Grade
ZINC1531087
Tox21_202164
Tox21_302935
BBL011381
BDBM50028842
LMFA12000004
MFCD00009513
STL146482
2-Heptanone, >=98%, FCC, FG
Methyl Amyl Ketone (Fragrance Grade)
AKOS000120708
UN 1110
NCGC00249180-01
NCGC00256611-01
NCGC00259713-01
VS-02935
FT-0612484
H0037
EN300-21047
C08380
A802193
Q517266
J-509557
n-Amyl methyl ketone [UN1110] [Flammable liquid]
Ick
MAK
hICK
LCK2
fj04c02
KIAA0936
kinase ICK
2-Heptanal
2-Heptanon
2-Heptanone
heptan-2-one
2-Oxoheptane
2-Ketoheptane
1-Methylhexanal
Methyl amyl ketone
Amyl-methyl-cetone
n-Amyl methyl ketone
Methyl n-pentyl ketone
Intestinal cell kinase
Laryngeal cancer kinase 2
amyl-methyl-cetone(french)