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Cyclohexanone

HCID 7967
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Basic information

CAS
108-94-1
Standard SMILES
O=C1CCCCC1
InChIKey
JHIVVAPYMSGYDF-UHFFFAOYSA-N
Molecular formula
C6H10O
Average molar mass
98.14 g/mol
Monoisotopic mass
98.07316494

Overview

Cyclohexanone appears as a colorless to pale yellow liquid with a pleasant odor. Less dense than water. Flash point 111 °F. Vapors heavier than air. Used to make nylon, as a chemical reaction medium, and as a solvent.

Names & identifiers

Preferred name
Cyclohexanone
IUPAC
cyclohexanone
English name
Cyclohexanone
Molecular formula
C6H10O
Molecular weight
98.14

Names & synonyms

CYCLOHEXANONE108-94-1KetohexamethylenePimelic ketoneSextoneNadoneAnoneAnonHytrol OCyclohexanonHexanonketocyclohexane
Show more names
HEXANONEFEMA 3909CYCLOHEXANONE REAGENT (ACS)
Pimelin ketoneoxocyclohexaneCicloesanoneCykloheksanonNCI-C55005RCRA waste number U057DTXSID6020359EPA Pesticide Chemical Code 025902

Database identifiers

CAS
108-94-1、9003-41-2
PubChem CID
7967
DTXSID
DTXSID6020359
ChEMBL
CHEMBL18850
ChEBI
CHEBI:17854
UNII
5QOR3YM052
EC Number
203-631-1
Nikkaji
J2.872J

Properties

Computed structural propertiesFilling in

XLogP
0.8
Topological polar surface area
17.1 Ų
Hydrogen bond donors
0
Hydrogen bond acceptors
1
Rotatable bonds
0
Heavy atoms
7
Formal charge
0
Complexity
68.2

Experimental & physicochemical properties

Chemical Classes · 2 items

Flammable agents - 2nd degree

Volatile Organic Compound (VOC)

DrugsPharmaceuticals -> Listed in ZINC15
SolventsSolvents -> Ketones (<C12)
SpringerMaterials PropertiesCoriolis coupling
FragrancesFragrance Ingredient (Cyclohexanone) -> IFRA transparency List
PesticidesPesticide -> EPA IRIS
LogP · 4 items

Log Kow= 0.81

0.81

0.81

0.81

Odor · 2 items

ODOR REMINISCENT OF PEPPERMINT & ACETONE

... Peppermint- or acetone-like odor.

Food AdditivesFLAVORING AGENT OR ADJUVANT -> FDA Substance added to food
Density

Safety & regulation

Safety information is for reference only and does not replace the supplier’s Safety Data Sheet (SDS), applicable regulations, or professional assessment.

GHS classification

GHS Classification · 6 items

Warning

H226: Flammable liquid and vapor [Warning Flammable liquids]

P210, P233, P240, P241, P242, P243, P261, P271, P280, P303+P361+P353, P304+P340, P317, P370+P378, P403+P235, and P501 (click each P-code to see the statement)

Danger

H226 (> 99.9%): Flammable liquid and vapor [Warning Flammable liquids]

P210, P233, P240, P241, P242, P243, P261, P264, P264+P265, P270, P271, P280, P301+P317, P302+P352, P303+P361+P353, P304+P340, P305+P354+P338, P317, P321, P330, P332+P317, P362+P364, P370+P378, P403+P235, and P501 (click each P-code to see the statement)

Hazard information

Regulatory Information · 6 items

Chemical: Cyclohexanone

Regulation (EC) No 1334/2008 (amended)

Cyclohexanone is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of Cyclohexanone are required to report information about their production and use of this chemical to the EPA under the Toxic Substances Control Act (TSCA). (40 eCFR Part 711)

REACH registered substance: Cyclohexanone (EC: 203-631-1)

Cyclohexanone: HSNO Approval: HSR001112 Approved with controls

The New Jersey Worker and Community Right to Know Act requires public and private employers to provide information about hazardous substances at their workplaces. (N.J.S.A. 34:5A-1 et. seq.)

Other Safety InformationIMAP assessments - Cyclohexanone: Human health tier I assessment
DOT LabelFlammable Liquid
Fire Hazards · 3 items

Excerpt from ERG Guide 127 [Flammable Liquids (Water-Miscible)]:

· HIGHLY FLAMMABLE: Will be easily ignited by heat, sparks or flames.

Flammable. Above 44 °C explosive vapour/air mixtures may be formed.

Chemistry & industry

Pharmacology

Biological Half-LifeFor 1,2-cyclohexanediol and 1,4-cyclohexanediol: 14-22 hours; [TDR, p. 434]
Metabolism/Metabolites · 5 items

/AFTER/ IP INJECTION OF 0.5 ML/MOUSE ... ONE OF METABOLIC PRODUCTS ... FOUND WAS ADIPIC ACID, PRESUMABLY DUE TO OXIDN OF CYCLOHEXANONE.

IT IS METABOLIZED BY REDUCTION INTO CYCLOHEXANOL & IS EXCRETED AS CYCLOHEXYLGLUCURONIDE.

... MINOR (1-2%) METABOLITES OF ... CYCLOHEXANONE & CYCLOHEPTANONE HAVE BEEN DETECTED IN RAT & RABBIT URINE. 2-HYDROXYCYCLOALKYLMERCAPTURIC ACIDS WHICH WERE PRESENT AS ... SULFATES ("DOUBLE CONJUGATES") ARE PRESUMABLY FORMED FROM DEHYDRATION OF CYCLOALKANOLS (MAJOR METABOLITES) TO CYCLOALKENES WITH SUBSEQUENT EPOXIDATION & MERCAPTURATION.

HEPATIC NICOTINAMIDE ADENINE DINUCLEOTIDE-DEPENDENT ALCOHOL DEHYDROGENASE ... HAS BEEN SHOWN TO BE RESPONSIBLE FOR METABOLISM OF ... CYCLOHEXANOL TO CORRESPONDING ... KETONE. SAME ENZYME IS CAPABLE OF CATALYZING REVERSE REACTION IN WHICH ... CYCLOHEXANONE ... /IS/ REDUCED TO ALCOHOL. EQUILIBRIUM OF SYSTEM FAVORS ... REVERSE REACTION & ... REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE PHOSPHATE ... /MAY/ FUNCTION AS COENZYME.

For more Metabolism/Metabolites (Complete) data for CYCLOHEXANONE (6 total), please visit the HSDB record page.

Absorption, Distribution and Excretion... ABSORPTION OF CYCLOHEXANONE THROUGH SKIN PRODUCES SAME EFFECTS AS BY OTHER ROUTES BUT DOSAGE REQUIRED IS LARGER.

Uses & manufacturing

Uses · 6 items

Has many uses as an industrial solvent; used as a paint remover and in printing inks; [ACGIH]

Painting (Solvents) [Category: Paint]

The active ingredient is no longer contained in any registered pesticide products ... "cancelled."

SOLVENT FOR CELLULOSE ACETATE, NITROCELLULOSE, WAXES, FAT, VINYL RESINS, CRUDE RUBBER, NATURAL RESINS, SHELLAC, DDT; IN PREPN OF CYCLOHEXANONE RESINS. 2,4-DINITROPHENYLHYDRAZONE DERIV AS STANDARD IN ELEMENTAL ANALYSIS.

METAL DEGREASING SOLVENT FOR LACQUERS, RESINS AND INSECTICIDES

SOLVENT FOR PVC POLYMERS & COPOLYMERS, LACQUERS; SPOT REMOVER AND DEGREASER FOR LEATHER

Related reactions

1,576 records
New reaction record
HRID 2352 reaction equation
HRID 2352As reactantuspto-grants-1998_03
HRID 2917 reaction equation
HRID 2917As reactantuspto-grants-1998_03
HRID 2993 reaction equation
HRID 2993As reactantuspto-grants-1998_03
HRID 6221 reaction equation
HRID 6221As reactantuspto-grants-1993_09
HRID 7339 reaction equation
HRID 7339As reactantuspto-grants-2006_08
HRID 9745 reaction equation
HRID 9745As productuspto-grants-2006_08
HRID 12046 reaction equation
HRID 12046As reactantuspto-grants-2010_06
HRID 12487 reaction equation
HRID 12487As reactantuspto-grants-2010_06
Page 1 of 197

Compound notes

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· 6 items

0.945 at 68 °F (USCG, 1999) - Less dense than water; will float

0.9421 @ 25 °C/4 °C; 0.9478 @ 20 °C/4 °C

Relative density (water = 1): 0.95

0.947-0.950

0.95

0.9421 @25 °C

Flavoring AgentsEU Flavoring substances
Viscosity2.2 mPa.s (=cP) @ 25 °C

Physicochemical properties

Melting point
-47 °C · -47 °C (lit.)
Boiling point
155 °C · 155 °C (lit.)
Density
0.947 g/mL · 0.947 g/mL at 25 °C (lit.)
vapor density
3.4 · 3.4 (vs air)
vapor pressure
3.4 mm · 3.4 mm Hg ( 20 °C)
refractive index
20 · n20/D 1.450(lit.)
FEMA
3909 · 3909 | CYCLOHEXANONE
FLAVIS Number
7.148 · 07.148 | Cyclohexanone
Flash point
116 °F · 116 °F
storage temp.
5 °C · Store at +5°C to +30°C.
solubility
90 g/l · 90g/l
pka
17 · 17(at 25℃)
form
Liquid
color
10 · APHA: ≤10
Relative polarity
0.281 · 0.281
PH
7 · 7 (70g/l, H2O, 20℃)
Odor
Like peppermint and acetone.
Odor Type
minty
biological source
synthetic
explosive limit
1.1 %, · 1.1%, 100°F
Water Solubility
150 g/L · 150 g/L (10 ºC)
Thermal Conductivity
0.144 W/ · 0.144 W/(m·K) at 25 ℃
Specific Heat Capacity
1.86 J/ · Cp(liquid): 1.86 J/(g·K), at 25℃
JECFA Number
1100 · 1100
Merck
14 · 14,2726
BRN
385735 · 385735
Henry's Law Constant
1.2 x · 1.2 x 10-5 atmm3/mol at 25 °C (Hawthorne et al., 1985) 6.92 x 10-5 atmm3/mol at 60.00 °C, 10.7 at 70.00 °C, 16.4 at 80.00 °C (headspace-GC, Hovorka et al., 2002)
Dielectric constant
18.2 · 18.2(20℃)
Exposure limits
50 mg/m3 · PC-TWA: 50 mg/m3
Stability
Stable. Combustible. Incompatible with strong oxidizing agents.
Major Application
flavors and fragrances
Cosmetics Ingredients Functions
PERFUMINGSOLVENT
InChI
1S/C6H10O/c7-6-4-2-1-3-5-6/h1-5H2
InChIKey
JHIVVAPYMSGYDF-UHFFFAOYSA-N
SMILES
O=C1CCCCC1
LogP
0.86 at · 0.86 at 25℃
Surface tension
33.74 mN/m · 33.74mN/m at 298.15K
CAS DataBase Reference
108 · 108-94-1(CAS DataBase Reference)
Substances Added to Food (formerly EAFUS)
CYCLOHEXANONE
FDA 21 CFR
177.225 · 177.2250
EWG's Food Scores
10 · 10
FDA UNII
5 QOR3YM052 · 5QOR3YM052
NIST Chemistry Reference
Cyclohexanone(108-94-1)
IARC
3 · 3 (Vol. 47, 71) 1999
EPA Substance Registry System
Cyclohexanone (108-94-1)
UNSPSC Code
41116107 · 41116107
NACRES
61 · NB.61
Symbol(GHS)
2 · GHS02,GHS06,GHS08
Signal word
Danger
Hazard statements
311 · H311+H331-H302-H315-H319-H361-H371-H370-H372-H341-H351-H335-H336-H305-H226
Precautionary statements
501 · P501-P270-P202-P240-P260-P210-P233-P201-P243-P241-P242-P271-P264-P280-P370+P378-P331-P337+P313-P305+P351+P338-P308+P311-P361+P364-P303+P361+P353-P332+P313-P301+P310-P304+P340+P311-P403+P233-P403+P235-P405
target organs
Respiratory system
PPE
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Hazard Codes
Xn
Risk Statements
10 · 10-20-41-38-20/21/22
Safety Statements
25 · 25-36/37/39-26
OEB
A
OEL
25 ppm · TWA: 25 ppm (100 mg/m3) [skin]
RIDADR
1915 · UN 1915
WGK Germany
1 · 1
RTECS
1050000 · GW1050000
Autoignition Temperature
788 °F · 788 °F
TSCA
TSCA listed
HS Code
2914 · 2914 22 00
HazardClass
3 · 3
PackingGroup
III
Storage Class
3 · 3 - Flammable liquids
Hazard Classifications
4 DermalAcute · Acute Tox. 4 DermalAcute Tox. 4 InhalationAcute Tox. 4 OralEye Dam. 1Flam. Liq. 3Skin Irrit. 2STOT SE 3
Hazardous Substances Data
108 · 108-94-1(Hazardous Substances Data)
Toxicity
50 orally · LD50 orally in rats: 1.62 ml/kg (Smyth)
IDLA
700 ppm · 700 ppm
REACH Registrations
Active
Limited Quantities
5 L · 5.0 L (1.3 gallons) (liquid)
Excepted Quantities
Max Inner Pack (30g or 30ml) and Max Outer Pack (1Kg or 1L)
Fire Potential · 2 items

MODERATE, WHEN EXPOSED TO HEAT OR FLAME; CAN REACT VIGOROUSLY WITH OXIDIZING MATERIALS ...

/CYCLOHEXANONE/ ... SHOULD NOT PRESENT A PROBLEM OF FLAMMABILITY UNLESS HANDLED AT ELEVATED TEMP.

Health Hazards · 2 items

Inhalation of vapors from hot material can cause narcosis. The liquid may cause dermatitis. (USCG, 1999)

· Inhalation or contact with material may irritate or burn skin and eyes.

Hazards Summary · 1 item

Liquid causes first degree burns on short exposure; [CHRIS] Animals become stuporous in high-dose inhalation studies and develop liver necrosis after high-dose feeding studies. [ACGIH] [Sanmartin O, et al. Occupational contact dermatitis from cyclohexanone as a PVC adhesive. Contact Dermatitis. 1992 Sep;27(3):189-90. No abstract available. Abstract in NIOSHTIC #179644]

DOT ID and Guide · 2 items

1915 127

1915 127

Reactive GroupKetones
EC ClassificationSymbol: Xn; R: 10-20; S: (2)-25
UN ClassificationUN Hazard Class: 3; UN Pack Group: III
Special Reports · 3 items

Occupational exposure to ketones, including cyclohexanone, is discussed.[NIOSH; Criteria Document: Ketones p.1-244 (1978) DHEW Pub. NIOSH 78-173.]

44 FR 31866 (6/1/79). The fourth report of the TSCA interagency testing committee to the administrator, EPA concerning cyclohexanone is discussed.

Spencer PS et al; Crit Rev Toxicol 7 (4): 279-356 (1980). Neurotoxicity of cyclohexanone is discussed.

Safety & protection

Fire Fighting · 2 items

Excerpt from ERG Guide 127 [Flammable Liquids (Water-Miscible)]:

Use alcohol-resistant foam, carbon dioxide, powder. In case of fire: keep drums, etc., cool by spraying with water.

First Aid Measures · 4 items

Fresh air, rest. Refer for medical attention.

Remove contaminated clothes. Rinse skin with plenty of water or shower. Refer for medical attention .

First rinse with plenty of water for several minutes (remove contact lenses if easily possible), then refer for medical attention.

Rinse mouth. Give one or two glasses of water to drink. Refer for medical attention .

Accidental Release Measures · 2 items

· CALL 911. Then call emergency response telephone number on shipping paper. If shipping paper not available or no answer, refer to appropriate telephone number listed on the inside back cover.

· ELIMINATE all ignition sources (no smoking, flares, sparks or flames) from immediate area.

First Aid · 3 items

EYES: First check the victim for contact lenses and remove if present. Flush victim's eyes with water or normal saline solution for 20 to 30 minutes while simultaneously calling a hospital or poison control center. Do not put any ointments, oils, or medication in the victim's eyes without specific instructions from a physician. IMMEDIATELY transport the victim after flushing eyes to a hospital even if no symptoms (such as redness or irritation) develop.

General First Aid:

(General first aid procedures)

Safe StorageFireproof. Separated from strong oxidants.
Exposure Control and Personal Protection · 3 items

· Wear positive pressure self-contained breathing apparatus (SCBA).

Biological Exposure Indices (BEI) [ACGIH] - 1,2-Cyclohexanediol (with hydrolysis) in urine: 80 mg/L (end of shift at end of workweek); Cyclohexanol (with hydrolysis) in urine: 8 mg/L (end of shift); See notations in ACGIH TLVs and BEIs.

756.0 [ppm]

Fire Fighting Procedures · 2 items

ALCOHOL FOAM, DRY CHEMICAL OR CARBON DIOXIDE

If material on fire or involved in fire: Do not extinguish fire unless flow can be stopped. Use water in flooding quantities as fog. Solid streams of water may be ineffective. Cool all affected containers with flooding quantities of water. Apply water from as far a distance as possible.

Storage ConditionsKeep containers closed; prohibit open flame. Store in cool and dark plane.
Cleanup Methods · 3 items

Remove all ignition sources. Ventilate area of spill or leak. For small quantities of liquids containing cyclohexanone, absorb on paper towels and place in an appropriate container. Place towels in a safe place (such as a fume hood) for evaporation. Allow sufficient time for evaporation of the vapors so that the hood ductwork is free from cyclohexanone vapors. Burn the paper in a suitable location away from combustible materials.

Large quantities of liquids containing cyclohexanone may be absorbed in vermiculite, dry sand, earth, or a similar material and placed in an appropriate container. Cyclohexanone should not be allowed to enter a confined space such as a sewer because of the possibility of an explosion. Cyclohexanone may be collected by vacuuming with an appropriate system. If a vacuum system is used, there should be no sources of ignition in the vicinity of the spill and flashback prevention devices should be provided.

Absorb on paper. Evaporate on a glass or an iron dish in hood. Burn the paper.

Nonfire Spill ResponseExcerpt from ERG Guide 127 [Flammable Liquids (Water-Miscible)]:
Disposal Methods · 3 items

Generators of waste (equal to or greater than 100 kg/mo) containing this contaminant, EPA hazardous waste number U057, F003, must conform with USEPA regulations in storage,transportation, treatment and disposal of waste.

Cyclohexanone is a waste chemical stream constituent which may be subjected to ultimate disposal by controlled incineration.

A good candidate for fluidized bed incineration at a temperature range of 450 to 980 °C and residence times of seconds for liquids and gases, and longer for solids. A good candidate for rotary kiln incineration at a temperature range of 820 to 1,600 °C and residence times of seconds for liquids and gases, and hours for solids. A good candidate for liquid injection incineration at a temperature range of 650 to 1,600 °C and a residence time of 0.1 to 2 seconds.

Spillage Disposal · 1 item

Personal protection: chemical protection suit and filter respirator for organic gases and vapours adapted to the airborne concentration of the substance. Remove all ignition sources. Ventilation. Collect leaking and spilled liquid in sealable containers as far as possible. Absorb remaining liquid in sand or inert absorbent. Then store and dispose of according to local regulations.

Toxicology

Toxicological InformationRanking: 544 (total points: 260.05)
Body Burden · 1 item

In a study including 42 production workers from a large video tape manufacturing plant and 17 workers from two plastic bag printing plants in Singapore, the mean cyclohexanone level in breath was 1.08 ppm with a range of 0-6.4 ppm(1). Environmental levels of cyclohexanone in the plants ranged from 0.1 to 36.0 ppm, with a mean of 9.04 ppm.

Target OrgansEyes, skin, respiratory system, central nervous system, liver, kidneys
Ecotoxicity ValuesLC50 Pimephales promelas (fathead minnow) 527 mg/l 96 hr flow-through bioassay, wt 0.12 g, water hardness 45.5 mg/l CaCO3, temp: 25 +/- 1 °C, pH 7.5, dissolved oxygen greater than 60% of saturation
Environmental Fate · 3 items

TERRESTRIAL FATE: Cyclohexanone is estimated to be highly mobile in soil(1,3,SRC). In view of its moderate vapor pressure(2) and low adsorption to soil(3), it would be expected to volatilize from surface soil. Although data are lacking, it may also undergo direct photolysis on the soil surface(4). Cyclohexanone is readily biodegradable according to aerobic screening tests(5-12) and therefore would be expected to biodegrade in soil(SRC).

AQUATIC FATE: If released in water, cyclohexanone would be slowly lost by volatilization. Its estimated half-lives in a model river and model lake are 4.1 and 33 days, respectively(1,2). Cyclohexanone is readily biodegradable according to aerobic screening tests(6) and in a die-away test performed using microorganisms from river water(3) and therefore, may be expected to biodegrade in natural waters. Adsorption to sediment(2,4) and bioconcentration(2,5) in aquatic organisms should be minimal(2) based upon its high water solubility(4) and low octanol/water partition coefficient(5).

ATMOSPHERIC FATE: In the atmosphere, cyclohexanone will degrade by reacting with photochemically-produced hydroxyl radicals. Its estimated half-life resulting from this reaction is 1.3 days(1,2).

Adverse EffectsNeurotoxin - Acute solvent syndrome
Exposure Routes · 2 items

The substance can be absorbed into the body by inhalation of its vapour, through the skin and by ingestion.

inhalation, skin absorption, ingestion, skin and/or eye contact

Signs and Symptoms · 5 items

Cough. Sore throat. Dizziness. Drowsiness.

MAY BE ABSORBED! Dry skin. Redness.

Redness. Pain.

Abdominal pain. Burning sensation.

irritation eyes, skin, mucous membrane; headache; narcosis, coma; dermatitis; In Animals: liver, kidney damage

Ongoing Test Status · 1 item

The following link will take the user to the National Toxicology Program (NTP) Test Agent Search Results page, which tabulates all of the "Standard Toxicology & Carcinogenesis Studies", "Developmental Studies", and "Genetic Toxicity Studies" performed with this chemical. Clicking on the "Testing Status" link will take the user to the status (i.e., in review, in progress, in preparation, on test, completed, etc.) and results of all the studies that the NTP has done on this chemical. [http://ntp-apps.niehs.nih.gov/ntp_tox/index.cfm?fuseaction=ntpsearch.searchresults&searchterm=108-94-1]

Effluent Concentrations · 2 items

In a comprehensive survey of wastewater from 4,000 industrial and publicly owned treatment works (POTWs) sponsored by the Effluent Guidelines Division of the U.S. EPA, cyclohexanone was identified in discharges of the following industrial category (positive occurrences, median concentration in ppb): leather tanning (4; 593), iron and steel manufacturing (2; 13.3), nonferrous metals (1; 28.1), paint and ink (5; 34.4), printing and publishing (2; 149), ore mining (2; 3.1), inorganic chemicals (5; 32.7), plastics and synthetics (23; 75.8), auto and other laundries (1; 1.2), pharmaceuticals (2; 44.2), explosives (1; 16.8), aluminum (4; 12.9), electronics (4; 11.9), organic chemicals (2; 62.7), and POTWs (12; 23.5)(1). Maximum effluent concentrations above 1000 ppb were observed in leather tanning (1,927 ppb), inorganic chemicals (10,256 ppb), and plastics and synthetics (2,345 ppb)(1).

Wastewater from advanced treatment facilities in Lake Tahoe, CA, Dallas, TX, and Blue Plains, Washington, DC contained cyclohexanone(1). A final effluent grab sample from the Danville, IL POTW collected in June 1980 contained cyclohexanone(2). Wastewaters from processing shale oil have been found to contain cyclohexanone(3,4). It was identified in leachate from a municipal landfill in Ontario, Canada(5). The concentration of cyclohexanone in active compost blower exhaust from a wastewater sludge composting facility was 13 ug/cu m(6).

EPA IRIS Information · 2 items

Cyclohexanone

5 mg/kg-day

Medical SurveillanceConsider the points of attack /respiratory system, eyes, skin, central nervous system/ in preplacement and periodic physical examinations.

Regulatory information

RCRA Requirements · 2 items

U057; As stipulated in 40 CFR 261.33, when CYCLOHEXANONE, as a commercial chemical product or manufacturing chemical intermediate or an off-specification commercial chemical product or a manufacturing chemical intermediate, becomes a waste, it must be managed according to Federal and/or State hazardous waste regulations. Also defined as a hazardous waste is any residue, contaminated soil, water, or other debris resulting from the cleanup of a spill, into water or on dry land, of this waste. Generators of small quantities of this waste may qualify for partial exclusion from hazardous waste regulations (40 CFR 261.5).

When cyclohexanone is a spent solvent, it is classified as a hazardous waste from a nonspecific source (F003), as stated in 40 CFR 261.31, and must be managed according to State and/or Federal hazardous waste regulations.

TSCA Requirements · 2 items

Section 8(a) of TSCA requires manufacturers of this chemical substance to report preliminary assessment information concerned with production, use, and exposure to EPA as cited in the preamble in 51 FR 41329.

Pursuant to section 8(d) of TSCA, EPA promulgated a model Health and Safety Data Reporting Rule. The section 8(d) model rule requires manufacturers, importers, and processors of listed chemical substances and mixtures to submit to EPA copies and lists of unpublished health and safety studies. Cyclohexanone is included on this list.

FIFRA Requirements · 3 items

As the federal pesticide law FIFRA directs, EPA is conducting a comprehensive review of older pesticides to consider their health and environmental effects and make decisions about their future use. Under this pesticide reregistration program, EPA examines health and safety data for pesticide active ingredients initially registered before November 1, 1984, and determines whether they are eligible for reregistration. In addition, all pesticides must meet the new safety standard of the Food Quality Protection Act of 1996. Pesticides for which EPA had not issued Registration Standards prior to the effective date of FIFRA, as amended in 1988, were divided into three lists based upon their potential for human exposure and other factors, with List B containing pesticides of greater concern and List D pesticides of less concern. Cyclohexanone is found on List C. Case No: 3053; Pesticide type: insecticide; Case Status: No products containing the pesticide are actively registered ... The case /is characterized/ as "cancelled." Under FIFRA, pesticide producers may voluntarily cancel their registered products. EPA also may cancel pesticide registrations if registrants fail to pay required fees or make/meet certain reregistration commitments, or if EPA reaches findings of unreasonable adverse effects.; Active ingredient (AI): Cyclohexanone; AI Status: The active ingredient is no longer contained in any registered pesticide products ... "cancelled."

Cyclohexanone is exempted from the requirement of a tolerance when used as a solvent or cosolvent in accordance with good agricultural practice as inert (or occasionally active) ingredients in pesticide formulations applied to growing crops only.

Cyclohexanone is exempted from the requirement of a tolerance when used as a solvent or cosolvent accordance with good agricultural practice as inert (or occasionally active) ingredients in pesticide formulations applied to animals.

Atmospheric Standards · 1 item

This action promulgates standards of performance for equipment leaks of Volatile Organic Compounds (VOC) in the Synthetic Organic Chemical Manufacturing Industry (SOCMI). These standards implement Section 111 of the Clean Air Act and are based on the Administrator's determination that emissions from the Synthetic Organic Chemical Manufacturing Industry cause, or contribute significantly to, air pollution which may reasonably be anticipated to endanger public health or welfare. The intended effect of these standards is to require all newly constructed, modified, and reconstructed Synthetic Organic Chemical Manaufacturing Industry process units to use the best demonstrated system of continuous emission reduction for equipment leaks of Volatile Organic Compounds, considering costs, non air quality health and environmental impact and energy requirements. Cyclohexanone is produced, as an intermediate or final product, by process units covered under this subpart. These standards of performance become effective upon promulgation but apply to affected facilities for which construction or modification commenced after January 5, 1981.

CERCLA Reportable Quantities · 1 item

Persons in charge of vessels or facilities are required to notify the National Response Center (NRC) immediately, when there is a release of this designated hazardous substance, in an amount equal to or greater than its reportable quantity of 5000 lb or 2700 kg. The toll free number of the NRC is (800) 424-8802; In the Washington D.C. metropolitan area (202) 426-2675. The rule for determining when notification is required is stated in 40 CFR 302.4 (section IV. D.3.b).

State Drinking Water Guidelines(FL) FLORIDA 35,000 ug/l

Safety data

OEB
A
OEL
TWA: 25 ppm (100 mg/m3) [skin]
PPE
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
wgk
1
IDLA
700 ppm
tsca
TSCA listed
rtecs
GW1050000
ridadr
UN 1915
hs_code
2914 22 00
Toxicity
LD50 orally in rats: 1.62 ml/kg (Smyth)
risk_code
10-20-41-38-20/21/22
Signal word
Danger
Symbol(GHS)
GHS02,GHS06,GHS08
hazard_code
Xn
safety_code
25-36/37/39-26
hazard_class
3
Storage Class
3 - Flammable liquids
packing_group
III
target organs
Respiratory system
Hazard statements
H311+H331-H302-H315-H319-H361-H371-H370-H372-H341-H351-H335-H336-H305-H226
Limited Quantities
5.0 L (1.3 gallons) (liquid)
Excepted Quantities
Max Inner Pack (30g or 30ml) and Max Outer Pack (1Kg or 1L)
REACH Registrations
Active
Hazard Classifications
Acute Tox. 4 DermalAcute Tox. 4 InhalationAcute Tox. 4 OralEye Dam. 1Flam. Liq. 3Skin Irrit. 2STOT SE 3
Autoignition Temperature
788 °F
Precautionary statements
P501-P270-P202-P240-P260-P210-P233-P201-P243-P241-P242-P271-P264-P280-P370+P378-P331-P337+P313-P305+P351+P338-P308+P311-P361+P364-P303+P361+P353-P332+P313-P301+P310-P304+P340+P311-P403+P233-P403+P235-P405
Hazardous Substances Data
108-94-1(Hazardous Substances Data)
U.S. Exports · 2 items

(1972) NEGLIGIBLE

(1975) NEGLIGIBLE

U.S. Imports · 2 items

(1972) NEGLIGIBLE

(1983) 1.91X10+9 g

U.S. Production · 6 items

2023: 1,000,000,000 - <2,500,000,000 lb

(1972) 3.56X10+11 G

(1975) 2.51X10+11 G

(1984) 3.61X10+11 g

(1992) 6.65x10+5 t (estimated)

(1992) 4.78X10+8 kg

Consumption Patterns · 2 items

95% FOR CAPROLACTAM AND ADIPIC ACID; 5% FOR SOLVENT APPLICATIONS (1973)

97% FOR NYLON 6 OR NYLON 66 MFR (1979)

Consumer UsesIntermediate
Industry UsesCleaning agent
Methods of Manufacturing · 3 items

CATALYTIC OXIDATION OF CYCLOHEXANE

OBTAINED FROM CYCLOHEXANOL BY CATALYTIC DEHYDROGENATION OR BY OXIDN (WHICH YIELDS CYCLOHEXANONE & ADIPIC ACID) ... BRITISH PATENT 310,055 (SCHERING-KAHLBAUM 1928); US PATENTS 2,223,493-4 (DU PONT 1940); 2,285,914 (DU PONT 1942).

CATALYTIC HYDROGENTION OF PHENOL OR BY THE CATALYTIC AIR-OXIDATION OF CYCLOHEXANE; MAY BE PREPARED BY EITHER THE CATAYLTIC DEHYDROGENATION OR OXIDATIVE DEHYDROGENATION OF CYCHEXANOL. THE PROCESS IS CARRIED OUT IN EITHER A LIQUID PHASE CATALYZED BY PALLADIUM OR CARBON, OR IN THE VAPOR PHASE CATALYZED BY PALLADIUM OR ALUMINA.

Formulations/Preparations · 2 items

Technical: 99.8%

COMMERCIAL: 89%; HIGH PURITY: 99.5%

Household ProductsInformation on 83 consumer products that contain Cyclohexanone in the following categories is provided:
Use Classification · 6 items

Fragrance Ingredients

Flavouring Agent -> FLAVOURING_AGENT -> JECFA Functional Classes

Flavoring Agents -> JECFA Flavorings Index

Flavouring Agent -> FLAVOURING_AGENT -> JECFA Functional Classes

Flavouring Agent -> FLAVOURING_AGENT -> JECFA Functional Classes

Flavouring Agent -> FLAVOURING_AGENT -> JECFA Functional Classes

General Manufacturing Information · 4 items

Printing Ink Manufacturing

Cyclohexanone: ACTIVE

IN LACQUER INDUST AS SLOWLY EVAPORATING IMPROVER, ALSO FOR LACQUERS & INSULATORS FOR HEAT & ELECTRICITY & FOR AUTOMOBILE LACQUERS. IN TEXTILE & PLASTIC INDUST, AS SPOTTING AGENT & RE-LUSTERING AGENT FOR CELLULOSE ACETATE SILK & IN SPRAY PAINTING OF FABRIC & PLASTIC TEXTILES. USED IN THE LEATHER INDUSTRY; AS A METAL DEGREASER; IN PAINT REMOVERS & IN PRINTING INKS.

DISTILLATION OF PIMELIC ACID SALTS WILL ALSO YIELD CYCLOHEXANONE.

Applications · 7 items

UsesCyclohexanone is an important chemical raw material, being the major intermediates of making nylon, caprolactam and adipic acid. It is also an important industrial solvent, for example, for paints, especially for those containing nitrocellulose, vinyl chloride polymers and their copolymers or methacrylate polymer paints. Used as an excellent solvent for pesticides such as organophosphate insecticide. It is used as a solvent for dyes, viscous solvents for piston aviation lubricants, solvents for greases, waxes and rubbers. Also used as leveling agent for dyeing and fading silk; degreasing agents for polishing metal; wood coloring paint; also used for cyclohexanone stripping, decontamination and spot removal. Cyclohexanone and cyanoacetic acid can have condensation reaction to generate cyclohexylidene acetic acid, and then followed by elimination and decarboxylation to get cyclohexene acetonitrile, and finally giving cyclohexene ethylamine by hydrogenation [3399-73-3]. Cyclohexene ethylamine is a intermediate for some drugs.

DescriptionCyclohexanone, a colorless liquid is a cyclic ketone. It is an important building block for the synthesis of a variety of organic compounds. Majority of the cyclohexanone synthesized is utilized as an intermediate in the synthesis of nylon.Used as a polyvinyl chloride (PVC) solvent, cyclohexanone caused contact dermatitis in a woman manufacturing PVC fluidotherapy bags. Cyclohexanone probably does not cross react with cyclohexanone resin. A cyclohexanone-derived resin used in paints and varnishes caused contact dermatitis in painters.

OccurrenceReported present in Cistus labdaniferus.

UsesIndustrial solvent for cellulose acetate resins, vinyl resins, rubber, and waxes; solventsealer for polyvinyl chloride; in printing industry; coating solvent in audio and videotape production

UsesCyclohexanone is used as an industrial solvent and paint remover. It acts as a precursor to nylon 6,6 and nylon 6 and cyclohexanone oxime, which gives caprolactam on rearrangement. Further, it is used as a chemical reaction medium, adhesives, sealants and agricultural products.

UsesCyclohexanone is used in the productionof adipic acid for making nylon; in thepreparation of cyclohexanone resins; and asa solvent for nitrocellulose, cellulose acetate,resins, fats, waxes, shellac, rubber, and DDT..

General DescriptionA colorless to pale yellow liquid with a pleasant odor. Less dense than water . Flash point 111°F. Vapors heavier than air. Used to make nylon, as a chemical reaction medium, and as a solvent.

Upstream & downstream products

Upstream raw materials

2-Hexanone1108Cyclohexanolheavy benzolHydrogen peroxideCyclohexaneWaterPETROLEUM ETHERBenzeneHydrogenCyclohexanolSodium hydroxidetert-Butyl chromate

Downstream products

Venlafaxine hydrochlorideETHYL 2-AMINO-4,5,6,7-TETRAHYDROBENZO[B]THIOPHENE-3-CARBOXYLATEPramipexoleε-Caprolactone(1S,2S)-(-)-1,2-Diphenyl-1,2-ethanediamineN,N-Dimethylcyclohexylamine1-Ethynyl-1-cyclohexanolCarbosulfanPorcelain-like coating2-ETHYLCYCLOHEXANONE2-AMINO-4,5,6,7-TETRAHYDRO-1-BENZOTHIOPHENE-3-CARBONITRILE(R)-2-AMINO-6-METHYLHEPTANE, 98% E.E., 953-AMINO-4,5,6,7-TETRAHYDRO-BENZO[B]THIOPHENE-2-CARBOXYLIC ACID METHYL ESTER2-(1-CYCLOHEXENYL)CYCLOHEXANONETramadol hydrochlorideClethodim1-NITROMETHYLCYCLOHEXANOL3-AMINO-5,6,7,8-TETRAHYDRO-3H-BENZO[4,5]THIENO[2,3-D]PYRIMIDIN-4-ONE1-AMINOMETHYL-1-CYCLOHEXANOL HYDROCHLORIDEMethoxydienone5,6,7,8-TETRAHYDRO-3H-BENZO[4,5]THIENO[2,3-D]-PYRIMIDIN-4-ONEPolyurethane varnish1-Hydroperoxycyclohexyl-1-hydroxycyclohexyl peroxideN-MethylcyclohexylamineOndansetronEthyl 2-oxocyclohexanecarboxylateVenlafaxine1-(1-PIPERIDINO)CYCLOHEXENEadhesive No.1 for shrink packaging2-Chlorocyclohexanone1,2,3,4-TETRAHYDRO-9-ACRIDINAMINE(1-HYDROXY-CYCLOHEXYL)-ACETONITRILE1,2-Cyclohexanedione2-(4-Aminobenzenesulfonamido)-4,6-dimethylpyrimidineDeflazacortCyclohexanone peroxide2-(HYDROXYMETHYL)CYCLOHEXANONECycloheptanoneAcid Orange 331-(aminomethyl)cyclohexan-1-ol

Additional notes

DefinitionChEBI: A cyclic ketone that consists of cyclohexane bearing a single oxo substituent.