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Basic information

  • Name:
  • Hexane

  • CAS No.:
  • 110-54-3

  • Formula:
  • C6H14
  • Synonyms:
  • NSC68472;Skellysolve B;n-Hexane;
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Specification

The IUPAC name of n-Hexane is hexane. With the CAS registry number 110-54-3, it is also named as Dipropyl. The product's categories are Analytical Chemistry; Solvents for HPLC & Spectrophotometry; Solvents for Spectrophotometry; Anhydrous Solvents; Synthetic Organic Chemistry; n-Paraffins (GC Standard); Standard Materials for GC. It is clear colorless liquids with a petroleum-like odor that is stable, incompatible with oxidizing agents, chlorine, fluorine, magnesium perchlorate. And n-Hexane is highly flammable, so people should keep it away from sources of ignition. What's more, it may be sensitive to light and may also be sensitive to prolonged exposure to heat.  

The other characteristics of n-Hexane can be summarized as: (1)ACD/LogP: 3.76; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): 3.764; (4)ACD/LogD (pH 7.4): 3.764; (5)ACD/BCF (pH 5.5): 427.313; (6)ACD/BCF (pH 7.4): 427.313; (7)ACD/KOC (pH 5.5): 2658.84; (8)ACD/KOC (pH 7.4): 2658.84; (9)#H bond acceptors: 0; (10)#H bond donors: 0; (11)#Freely Rotating Bonds: 3; (12)Index of Refraction: 1.384; (13)Molar Refractivity: 29.846 cm3; (14)Molar Volume: 127.576 cm3; (15)Polarizability: 11.832×10-24 cm3; (16)Surface Tension: 20.32 dyne/cm; (17)Enthalpy of Vaporization: 28.85 kJ/mol; (18)Vapour Pressure: 150.927 mmHg at 25°C; (19)Rotatable Bond Count: 3; (20)Exact Mass: 86.10955; (21)MonoIsotopic Mass: 86.10955; (22)Heavy Atom Count: 6; (23)Complexity: 12.

Preparation of n-Hexane: It is produced by the refining of crude oil. The exact composition of the fraction depends largely on the source of the oil (crude or reformed) and the constraints of the refining. The industrial product (usually around 50% by weight of the straight-chain isomer) is the fraction boiling at 65–70 °C.

Uses of n-Hexane: It is used in solvents to extract oils for cooking and as a cleansing agent for shoe, furniture and textile manufacturing. It is mostly used in gasoline. They are also used as a solvent and as a medium for various polymerization reactions. A typical laboratory use of hexanes is to extract oil and grease contaminants from water and soil for analysis. In addition, n-Hexane can react with hex-1-ene to get benzene. This reaction needs reagent H2 and catalytic agent Pt-Re/h-Al2O3 at temperature of 510 °C. The yield is 60%.

When you are using this chemical, please be cautious about it as the following:
It is not only irritating to eyes, respiratory system and skin, but also very toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment. And it is also risk of impaired fertility. In addition, this chemical may cause lung damage if swallowed. So people should not empty into drains and take precautionary measures against static discharges. If swallowed, do not induce vomitting; seek medical advice immediately and show this container or label. If you want to contact this product, you must wear suitable protective clothing, gloves and eye/face protection. In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.) This material and its container must be disposed of as hazardous waste. Avoid release to the environment. Refer to special instructions / safety data sheets. 

People can use the following data to convert to the molecule structure. 
1. SMILES:CCCCCC
2. InChI:InChI=1/C6H14/c1-3-5-6-4-2/h3-6H2,1-2H3
3. InChIKey:VLKZOEOYAKHREP-UHFFFAOYAD

The following are the toxicity data which has been tested.

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
human TCLo inhalation 190ppm/8W (190ppm) PERIPHERAL NERVE AND SENSATION: STRUCTURAL CHANGE IN NERVE OR SHEATH American Journal of Industrial Medicine. Vol. 10, Pg. 111, 1986.
 
mouse LCLo inhalation 120gm/m3 (120000mg/m3) BEHAVIORAL: GENERAL ANESTHETIC

CARDIAC: OTHER CHANGES

LUNGS, THORAX, OR RESPIRATION: RESPIRATORY DEPRESSION
Naunyn-Schmiedeberg's Archiv fuer Experimentelle Pathologie und Pharmakologie. Vol. 143, Pg. 223, 1929.
mouse LDLo intravenous 831mg/kg (831mg/kg) BEHAVIORAL: ALTERED SLEEP TIME (INCLUDING CHANGE IN RIGHTING REFLEX) Acta Pharmacologica et Toxicologica. Vol. 37, Pg. 56, 1975.
 
rabbit LDLo intravenous 132mg/kg (132mg/kg)   Haematologica. Vol. 58, Pg. 491, 1973.
rat LC50 inhalation 48000ppm/4H (48000ppm)   Annual Review of Pharmacology and Toxicology. Vol. 22, Pg. 145, 1982.
rat LD50 oral 25gm/kg (25000mg/kg)   Industrial Health. Vol. 32, Pg. 145, 1994.
rat LDLo intraperitoneal 9100mg/kg (9100mg/kg)   Toxicology and Applied Pharmacology. Vol. 1, Pg. 156, 1959.

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