ChemicalBook >> CAS DataBase List >>Cyclohexane

Cyclohexane

CAS No.
110-82-7
Chemical Name:
Cyclohexane
Synonyms
cyclohexan;NAPHTHENE;HEXAMETHYLENE;Cykloheksan;hexamethylen;CYCLOHEXANE-205;HEXAHYDROBENZENE;ohexane;Cicloesano;Cyclohesan
CBNumber:
CB4193601
Molecular Formula:
C6H12
Lewis structure
c6h12 lewis structure
Molecular Weight:
84.16
MDL Number:
MFCD00003814
MOL File:
110-82-7.mol
MSDS File:
SDS
Last updated:2024-03-14 15:18:26

Cyclohexane Properties

Melting point 4-7 °C (lit.)
Boiling point 80.7 °C (lit.)
Density 0.779 g/mL at 25 °C (lit.)
vapor density 2.9 (vs air)
vapor pressure 168.8 mm Hg ( 37.7 °C)
refractive index n20/D 1.426(lit.)
Flash point -1 °F
storage temp. Store at +5°C to +30°C.
solubility ethanol: miscible(lit.)
form Liquid
color colorless
Relative polarity 0.006
Odor resembling benzene; mild, sweet, resembling chloroform.
Odor Threshold 2.5ppm
explosive limit 1.2-8.3%(V)
Water Solubility PRACTICALLY INSOLUBLE
FreezingPoint 6.554℃
λmax λ: 210 nm Amax: ≤1.00
λ: 220 nm Amax: ≤0.50
λ: 230 nm Amax: ≤0.20
λ: 235 nm Amax: ≤0.10
λ: 240 nm Amax: ≤0.08
λ: 250 nm Amax: ≤0.03
λ: 255 nm Amax: ≤0.01
Merck 14,2723
BRN 1900225
Henry's Law Constant 1.03, 1.26, 1.40, 1.77, and 2.23 at 10, 15, 20, 25, and 30 °C, respectively (EPICS, Ashworth et al., 1988) 0.54, 0.69, 0.82, 1.43, and 1.79 at 2.0, 6.0, 10.0, 18.0, and 25.0 °C, respectively (Dewulf et al.,1999)
Exposure limits TLV-TWA 300 ppm (~1050 mg/m3) (ACGIH, OSHA, and NIOSH); IDLH 10,000 ppm (NIOSH).
Dielectric constant 2.0(20℃)
Stability Volatile
InChIKey XDTMQSROBMDMFD-UHFFFAOYSA-N
LogP 3.44 at 20℃
Substances Added to Food (formerly EAFUS) CYCLOHEXANE
FDA 21 CFR 175.105; 176.200; 73.1
CAS DataBase Reference 110-82-7(CAS DataBase Reference)
EWG's Food Scores 2
FDA UNII 48K5MKG32S
NIST Chemistry Reference Cyclohexane(110-82-7)
EPA Substance Registry System Cyclohexane (110-82-7)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictogramsGHS hazard pictogramsGHS hazard pictograms
GHS02,GHS07,GHS08,GHS09
Signal word  Danger
Hazard statements  H225-H304-H315-H336-H410
Precautionary statements  P210-P233-P273-P301+P310-P303+P361+P353-P331
Hazard Codes  F,Xn,N
Risk Statements  11-38-50/53-65-67-20
Safety Statements  9-16-25-33-60-61-62
RIDADR  UN 1145 3/PG 2
WGK Germany  2
RTECS  GU6300000
3-10
Autoignition Temperature 500 °F
TSCA  Yes
HS Code  2902 11 00
HazardClass  3
PackingGroup  II
Toxicity LC in mice: ~60-70 mg/l air (Lazarew)
IDLA 1,300 ppm [10% LEL]
NFPA 704
3
1 0

Cyclohexane price More Price(92)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich CX2290 Cyclohexane Meets ACS Specifications, Meets Reagent Specifications for testing USP/NF monographs GR ACS 110-82-7 1L $227 2024-03-01 Buy
Sigma-Aldrich CX2290 Cyclohexane Meets ACS Specifications, Meets Reagent Specifications for testing USP/NF monographs GR ACS 110-82-7 4L $392 2024-03-01 Buy
Sigma-Aldrich CX2290 Cyclohexane Meets ACS Specifications, Meets Reagent Specifications for testing USP/NF monographs GR ACS 110-82-7 200L $5490 2024-03-01 Buy
Sigma-Aldrich CX2286 Cyclohexane OmniSolv? 110-82-7 4L $403 2024-03-01 Buy
Sigma-Aldrich 33117 Cyclohexane puriss. p.a., ACS reagent, ≥99.5% (GC) 110-82-7 6X1L $268.8 2024-03-01 Buy
Product number Packaging Price Buy
CX2290 1L $227 Buy
CX2290 4L $392 Buy
CX2290 200L $5490 Buy
CX2286 4L $403 Buy
33117 6X1L $268.8 Buy

Cyclohexane Chemical Properties,Uses,Production

Description

Cyclohexane is obtained by the distillation of petroleum or by hydrogenation of benzene. It constitutes 0.5–1.0% of petroleum

Chemical Properties

Cyclohexane is a colorless liquid with a mild, sweet odor.

Physical properties

Colorless liquid with a sweet, chloroform-like odor. A detection odor threshold concentration of 2,700 mg/m3 (784 ppmv) was experimentally determined by Dravnieks (1974). An odor threshold concentration of 2.7 ppbv was reported by Nagata and Takeuchi (1990).

Uses

Suitable for HPLC, spectrophotometry, environmental testing

Uses

Cyclohexane is a petroleum product obtainedby distilling C4- 400°F boiling rangenaphthas, followed by fractionation andsuperfractionation; also formed by catalytichydrogenation of benzene. It is usedextensively as a solvent for lacquers andresins, as a paint and varnish remover, andin the manufacture of adipic acid, benzene,cyclohexanol, and cyclohexanone.

Uses

Solvent for lacquers and resins. Paint and varnish remover. In the extraction of essential oils. In analytical chemistry for mol wt determinations (cryoscopic constant 20.3). In the manufacture of adipic acid, benzene, cyclohexyl chloride, nitrocyclohexane, cyclohexanol and cyclohexanone. In the manufacture of solid fuel for camp stoves. In fungicidal formulations (possesses slight fungicidal action). In the industrial recrystallization of steroids.

Definition

cyclohexane: A colourless liquidcycloalkane, C6H12; r.d. 0.78; m.p.6.5°C; b.p. 81°C. It occurs in petroleumand is made by passing benzeneand hydrogen under pressureover a heated Raney nickel catalyst at150°C, or by the reduction of cyclohexanone.It is used as a solvent andpaint remover and can be oxidizedusing hot concentrated nitric acid tohexanedioic acid (adipic acid). The cyclohexanering is not planar and canadopt boat and chair conformations;in formulae it is representedby a single hexagon.

Definition

A colorless liquid alkane that is commonly used as a solvent and in the production of hexanedioic acid (adipic acid) for the manufacture of nylon. Cyclohexane, itself, is manufactured by the reformation of longer chain hydrocarbons present in crude-oil fractions. It is also interesting from a structural point of view, existing as a ‘puckered’ six-membered ring, having all bonds between carbon atoms at 109.9° (the tetrahedral angle). The molecule undergoes rapid interconversion between two ‘chair-like’ CONFORMATIONS, which are energetically equivalent, passing through a ‘boat-like’ structure of higher energy. It is commonly represented by a hexagon.

Production Methods

Cyclohexane is fractionated from crude oil and may be released wherever petroleum products are refined, stored, and used. Another large source of general release is in exhaust gases from motor vehicles. It is prepared synthetically from benzene, by hydrocracking of cyclopentane, or from toluene by simultaneous dealkylation and double bond hydrogenation.

Definition

ChEBI: An alicyclic hydrocarbon comprising a ring of six carbon atoms; the cyclic form of hexane, used as a raw material in the manufacture of nylon.

General Description

A clear colorless liquid with a petroleum-like odor. Used to make nylon, as a solvent, paint remover, and to make other chemicals. Flash point -4°F. Density 6.5 lb / gal (less than water) and insoluble in water. Vapors heavier than air.

Air & Water Reactions

Highly flammable. Insoluble in water.

Reactivity Profile

Liquid nitrogen dioxide was fed into a nitration column containing hot Cyclohexane, due to an error. An explosion resulted [MCA Case History 128(1962)] Incompatible with strong oxidizers.

Health Hazard

Dizziness, with nausea and vomiting. Concentrated vapor may cause unconsciousness and collapse.

Health Hazard

Cyclohexane is an acute toxicant of loworder. It is an irritant to the eyes and respiratorysystem. Exposure to a 1–2% concentrationin air caused lethargy, drowsiness,and narcosis in test animals. The lethal concentrationfor a 1-hour exposure in mice isestimated at around 30,000 ppm. Ingestionof cyclohexane exhibited low toxic effects intest species. The LD50 values in the literature show a wide variation. It may be detectedfrom its odor at 300 ppm concentration.

Flammability and Explosibility

Highly flammable

Chemical Reactivity

Reactivity with Water: No reaction; Reactivity with Common Materials: No reaction; Stability During Transport: Stable; Neutralizing Agents for Acids and Caustics: Not pertinent; Polymerization: Not pertinent; Inhibitor of Polymerization: Not pertinent.

Safety Profile

Poison by intravenous route, Moderately toxic by ingestion. A systemic irritant by inhalation and ingestion. A skin irritant. Mutation data reported. Flammable liquid. Dangerous fire hazard when exposed to heat or flame; can react with oxidming materials. Moderate explosion hazard in the form of vapor when exposed to flame. When mixed hot with liquid dinitrogen tetraoxide an explosion can result. To fight fire, use foam, CO2, dry chemical, spray, fog. When heated to decomposition it emits acrid smoke and fumes.

Potential Exposure

Cyclohexane is used as a chemical intermediate; as a solvent for fats, oils, waxes, resins, cer- tain synthetic rubbers; and as an extractant of essential oils in the perfume industry.

First aid

If this chemical gets into the eyes, remove anycontact lenses at once and irrigate immediately for at least15 min, occasionally lifting upper and lower lids. Seek medical attention immediately. If this chemical contacts the skin,remove contaminated clothing and wash immediately withsoap and water. Seek medical attention immediately. If thischemical has been inhaled, remove from exposure, begin rescue breathing (using universal precautions, including resuscitation mask) if breathing has stopped and CPR if heart actionhas stopped. Transfer promptly to a medical facility. Whenthis chemical has been swallowed, get medical attention. Donot induce vomiting

Carcinogenicity

No tumor-promoting activity was observed in mice receiving one 60 mL application of 0.3% DMBA in benzene followed by a 60 mL application of cyclohexane twice weekly for 50 weeks.

Source

Schauer et al. (1999) reported cyclohexane in a diesel-powered medium-duty truck exhaust at an emission rate of 210 μg/km.
California Phase II reformulated gasoline contained cyclohexane at a concentration of 8,900 mg/kg. Gas-phase tailpipe emission rates from gasoline-powered automobiles with and without catalytic converters were 1.44 and 238.0 mg/km, respectively (Schauer et al., 2002).

Environmental Fate

Biological. Microbial degradation products reported include cyclohexanol (Dugan, 1972; Verschueren, 1983), 1-oxa-2-oxocycloheptane, 6-hydroxyheptanoate, 6-oxohexanoate, adipic acid, acetyl-CoA, succinyl-CoA (quoted, Verschueren, 1983), and cyclohexanone (Dugan, 1972; Keck et al., 1989).
Photolytic. The following rate constants were reported for the reaction of cyclohexane and OH radicals in the atmosphere: 5.38 x 10-12 cm3/molecule?sec at 295 K (Greiner, 1970); 6.7 x 10-12 cm3/molecule?sec at 300 K (Darnall et al., 1978); 6.69 x 10-12 cm3/molecule?sec at 298 (DeMore and Bayes, 1999); 7.0 x 10-12 cm3/molecule?sec (Atkinson et al., 1979); 7.49 x 10-12 cm3/molecule?sec (Atkinson, 1990). A photooxidation reaction rate constant of 1.35 x 10-16 cm3/molecule?sec was reported for the reaction of cyclohexane with NO3 in the atmosphere (Atkinson, 1991).
Chemical/Physical. The gas-phase reaction of cyclohexane with OH radicals in the presence of nitric oxide yielded cyclohexanone and cyclohexyl nitrate as the major products (Aschmann et al., 1997).
Cyclohexane will not hydrolyze because it has no hydrolyzable functional group.

storage

Color Code—Red: Flammability Hazard: Store ina flammable liquid storage area or approved cabinet awayfrom ignition sources and corrosive and reactive materials.Prior to working with cyclohexane you should be trained onits proper handling and storage. Before entering confinedspace where cyclohexane may be present, check to makesure that an explosive concentration does not exist.Cyclohexane must be stored to avoid contact with oxidizers(such as perchlorates, peroxides, permanganates, chlorates,and nitrates), since violent reactions occur. Store in tightlyclosed containers in a cool well-ventilated area away fromheat. Metal containers involving the transfer of this chemical should be grounded and bonded. Where possible, automatically pump liquid from drums or other storagecontainers to process containers. Drums must be equippedwith self-closing valves, pressure vacuum bungs, and flamearresters. Use only nonsparking tools and equipment, especially when opening and closing containers of this chemical. Sources of ignition, such as smoking and open flames,are prohibited where this chemical is used, handled, orstored in a manner that could create a potential fire orexplosion hazard. Wherever cyclohexane is used, handled,manufactured, or stored, use explosion-proof electricalequipment and fittings.

Shipping

UN1145 Cyclohexane, Hazard Class: 3; Labels: 3-Flammable liquid.

Purification Methods

It is best to purify it by washing with conc H2SO4 until the washings are colourless, followed by water, aqueous Na2CO3 or 5% NaOH, and again water until neutral. It is then dried with P2O5, Linde type 4A molecular sieves, CaCl2, or MgSO4 then Na and distilled. Cyclohexane has been refluxed with, and distilled from Na, CaH2, LiAlH4 (which also removes peroxides), sodium/potassium alloy, or P2O5. Traces of *benzene can be removed by passage through a column of silica gel that has been freshly heated: this gives material suitable for ultraviolet and infrared spectroscopy. If there is much *benzene in the cyclohexane, most of it can be removed by a preliminary treatment with nitrating acid (a cold mixture of 30mL conc HNO3 and 70mL of conc H2SO4) which converts *benzene into nitrobenzene. The impure cyclohexane and the nitrating acid are placed in an ice bath and stirred vigorously for 15minutes, after which the mixture is allowed to warm to 25o during 1hour. The cyclohexane is decanted, washed several times with 25% NaOH, then water, dried with CaCl2, and distilled from sodium. Carbonyl-containing impurities can be removed as described for chloroform. Other purification procedures include passage through columns of activated alumina and repeated crystallisation by partial freezing. Small quantities may be purified by chromatography on a Dowex 710-Chromosorb W gas-liquid chromatographic column. Flammable liquid. [Sabatier Ind Eng Chem 18 1005 1926, Schefland & Jacobs The Handbook of Organic Solvents (Van Nostrand) p592 1953, Beilstein 5 IV 27.] Rapid purification: Distil, discarding the forerun. Stand distillate over Grade I alumina (5% w/v) or 4A molecular sieves.

Toxicity evaluation

If released to air, cyclohexane will exist solely as a vapor in the ambient atmosphere, and will be degraded in the atmosphere by reaction with photochemically produced hydroxyl radicals, though direct photolysis is not expected due to the lack of absorption in the environmental spectrum. Volatilization from water surfaces is expected to be an important fate for this compound, and half-lives in a model river and lake are expected to be 3 h and ~3.5 days respectively. Adsorption to suspended solids and sediments is also expected, though hydrolysis in the environment is unlikely due to the lack of hydrolyzable functional groups.
The potential for bioconcentration and bioaccumulation of cyclohexane in aquatic organisms is moderate. It is highly resistant to biodegradation and is catabolized chiefly by cooxidation.

Incompatibilities

May form explosive mixture with air. Contact with oxidizers, nitrogen dioxide, and oxygen can cause fire and explosion hazard. Can explode in heat when mixed with dinitrogen tetraoxide liquid.

Waste Disposal

Dissolve or mix the material with a combustible solvent and burn in a chemical incinera- tor equipped with an afterburner and scrubber. All federal, state, and local environmental regulations must be observed.

108-93-0
110-82-7
Synthesis of Cyclohexane from Cyclohexanol
Global( 786)Suppliers
Supplier Tel Email Country ProdList Advantage
Shandong Yanshuo Chemical Co., Ltd.
+86-18678179670 +86-18615116763 sales@yanshuochem.com China 101 58
Hebei Duling International Trade Co. LTD
+8618032673083 sales05@hbduling.cn China 15745 58
PT CHEM GROUP LIMITED
+86-85511178 +86-85511178 peter68@ptchemgroup.com China 35453 58
Hebei Mojin Biotechnology Co., Ltd
+8613288715578 sales@hbmojin.com China 12456 58
Hebei Jingbo New Material Technology Co., Ltd
+8619931165850 hbjbtech@163.com China 1000 58
Henan Fengda Chemical Co., Ltd
+86-371-86557731 +86-13613820652 info@fdachem.com China 7786 58
Capot Chemical Co.,Ltd.
571-85586718 +8613336195806 sales@capotchem.com China 29797 60
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512 info@tianfuchem.com China 21691 55
Shanghai Time Chemicals CO., Ltd.
+86-021-57951555 +8617317452075 jack.li@time-chemicals.com China 1807 55
Hefei TNJ Chemical Industry Co.,Ltd.
+86-0551-65418679 +86-18949832763 info@tnjchem.com China 2989 55

Related articles

  • Toxicity of Cyclohexane
  • Cyclohexane is obtained by the distillation of petroleum or by hydrogenation of benzene. It constitutes 0.5–1.0% of petroleum.
  • Jan 13,2022
  • Uses and safety of Cyclohexane
  • Cyclohexane is used as a solvent to dissolve cellulose ethers, lacquers, resins, fats, waxes, oils, bitumen and crude rubber. ....
  • Jan 10,2022

Related Qustion

View Lastest Price from Cyclohexane manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Cyclohexane pictures 2024-04-24 Cyclohexane
110-82-7
US $230.00 / ton 1ton 99% 3000tons Hebei Dangtong Import and export Co LTD
Cyclohexane pictures 2023-12-26 Cyclohexane
110-82-7
US $100.00-1.00 / KG 1KG 99% g-kg-tons, free sample is available Henan Fengda Chemical Co., Ltd
Cyclohexane pictures 2023-12-26 Cyclohexane
110-82-7
US $9.00 / kg 1kg 99% 20000 Hebei Jingbo New Material Technology Co., Ltd
  • Cyclohexane pictures
  • Cyclohexane
    110-82-7
  • US $230.00 / ton
  • 99%
  • Hebei Dangtong Import and export Co LTD
  • Cyclohexane pictures
  • Cyclohexane
    110-82-7
  • US $100.00-1.00 / KG
  • 99%
  • Henan Fengda Chemical Co., Ltd
  • Cyclohexane pictures
  • Cyclohexane
    110-82-7
  • US $9.00 / kg
  • 99%
  • Hebei Jingbo New Material Technology Co., Ltd
CYCLOHEXANE-195 CYCLOHEXANE HEXANAPHTHENE HEXANAPHTHALENE Benzene, hexahydro- benzenehexahydride Hexahydrobenzol hexamethylenecarbamide Rcra waste number U056 rcrawastenumberu056 CYCLOHEXANE FOR RESIDUE ANALYSIS Cyclohexane, conform to ACS, for spectroscopy, 99+% Cyclohexane, for analysis, 99.5% Cyclohexane, for HPLC, 99.8% Cyclohexane, for spectroscopy, 99+% Cyclohexane, pure, 99+% Cyclohexane, suitable for residue and pesticides analysis, for residue analysis Cyclohexane, water <50 ppm, extra dry over mol. sieve, 99.5% Cyclohexane, water <50 ppm, extra dry, 99.5% CYCLOHEXANE DISTILLED IN GLASS CYCLOHEXANE HPLC CYCLOHEXANE REAGENT (ACS) cyclohexane, environmental grade cyclohexane, hplc grade CYCLOHEXANE,ANHYDROUS CYCLOHEXANE,OMNISOLV CYCLOHEXANE,PESTISOLV CYCLOHEXANE,PRACTICAL CYCLOHEXANE,SPECTROPHOTOMETRICGRADE,ACS CYCLOHEXANE,SPECTROSOLV Benzene, hexahydro- (I) Cyclohexane (I) CYCLOHEXANE: ANALYTICAL REAGENT Cyclohexane, Environmental Grade, 99.7+% Cyclohexane, HPLC Grade, 99.9+% Cyclohexane, ACS, 99+% Cyclohexane, HPLC Grade, 99% min cyclohexane B&J brand 4 L CYCLOHEXANE ULTRA RESI-ANAL. Cyclohexane [for HPLC Solvent] Cyclohexane, 99.5%, for analysis Cyclohexane, 99.8%, for HPLC Cyclohexane, 99.5%, water <50 ppm, extra dry over molecular sieve Cyclohexane, pure Cyclohexane, for spectroscopy Cyclohexane, for analysis Cyclohexane, AcroSeal, Extra Dry Cyclohexane, AcroSeal, Extra Dry over Molecular Sieve Cyclohexane, conform to ACS, for spectroscopy CYCLOHEXANE extrapure AR Cyclohexane, Spectrophotometric Grade, 99+% Cyclohexane, anhydrous, 99+% Cyclohexane,99.5%,extra pure Cyclohexane,for residue analysis,suitable forresidue and pesticides analysis Cyclohexane,99.5%,Extra Dry over Molecular Sieve Cyclohexane,99.5%,Extra Dry Cyclohexane,99+%,for spectroscopy,conform toACS Cyclohexane ,99.7% [ACS/HPLC certified]