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2,2-Dimethylbutane

CAS No.
75-83-2
Chemical Name:
2,2-Dimethylbutane
Synonyms
NEOHEXANE;Trimethylpropane;neobutan;NEOBUTANE;(CH3)3CCH2CH3;2.2-DiMethylbu;tert-Butylethane;2-Ethylisobutane;2,2-dimethyl-butan;3,3-DIMETHYLBUTANE
CBNumber:
CB7280708
Molecular Formula:
C6H14
Lewis structure
c6h14_3.0 lewis structure
Molecular Weight:
86.18
MDL Number:
MFCD00009321
MOL File:
75-83-2.mol
Last updated:2023-12-25 13:23:17

2,2-Dimethylbutane Properties

Melting point −100 °C(lit.)
Boiling point 50 °C(lit.)
Density 0.649 g/mL at 25 °C(lit.)
vapor density 2.97 (vs air)
vapor pressure 5.35 psi ( 20 °C)
refractive index n20/D 1.369(lit.)
Flash point <−30 °F
storage temp. Flammables area
solubility In methanol: 590 and 800 g/L at 5 and 10 °C, respectively. Miscible at higher temperatures (Kiser et al., 1961). Miscible with other aliphatic hydrocarbons, e.g., pentane, hexane, heptane, etc.
form Liquid
pka >14 (Schwarzenbach et al., 1993)
color Clear colorless to slightly yellow
explosive limit ~7.7%
Odor Threshold 20ppm
Water Solubility insoluble
BRN 1730736
Henry's Law Constant 1.69(atm?m3/mol) at 25 °C (Mackay and Shiu, 1981)
Exposure limits ACGIH TLV: TWA and STEL for all isomers except n-hexane are 500 and 1,000 ppm, respectively (adopted).
Dielectric constant 1.8700000000000001
Stability Stable, but may be moisture sensitive. Highly flammable. Incompatible with strong oxidizing agents.
CAS DataBase Reference 75-83-2(CAS DataBase Reference)
FDA UNII 07L56L3MP2
NIST Chemistry Reference Butane, 2,2-dimethyl-(75-83-2)
EPA Substance Registry System 2,2-Dimethylbutane (75-83-2)

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-H411
Precautionary statements  P210-P233-P273-P301+P310-P303+P361+P353-P331
Hazard Codes  F,Xn,N
Risk Statements  11-38-51/53-65-67
Safety Statements  9-16-29-33-61-62
RIDADR  UN 1208 3/PG 2
OEB A
OEL TWA: 100.0 ppm; 350.0 mg/m3, STEL: 510.0 ppm; 1800.0 mg/m3
WGK Germany  3
RTECS  EJ9300000
Autoignition Temperature 797 °F
HazardClass  3
PackingGroup  II
HS Code  29011000
Toxicity Reported as an impurity (0.2 wt %) in 99.0–99.7 wt % 2,3-dimethylbutane (Chevron Phillips, 2004).
NFPA 704
3
2 0

2,2-Dimethylbutane price More Price(16)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 39730 2,2-Dimethylbutane analytical standard 75-83-2 5ml $74.2 2024-03-01 Buy
Sigma-Aldrich 39730 2,2-Dimethylbutane analytical standard 75-83-2 10ml $140 2024-03-01 Buy
TCI Chemical D0689 2,2-Dimethylbutane >97.0%(GC) 75-83-2 25mL $73 2024-03-01 Buy
TCI Chemical D0689 2,2-Dimethylbutane >97.0%(GC) 75-83-2 100mL $229 2024-03-01 Buy
TRC D462315 2,2-Dimethylbutane 75-83-2 5mL $65 2021-12-16 Buy
Product number Packaging Price Buy
39730 5ml $74.2 Buy
39730 10ml $140 Buy
D0689 25mL $73 Buy
D0689 100mL $229 Buy
D462315 5mL $65 Buy

2,2-Dimethylbutane Chemical Properties,Uses,Production

Chemical Properties

2,2-dimethylbutane is the chain isomeric form of hexane. It is a colorless and flammable liquid with a specific gravity of 0.6444. Insoluble in water, miscible with alcohol, ether, acetone, benzene and petroleum ether. The solubility is similar to that of hexane and 2-methylpentane.

Physical properties

Clear, colorless liquid with a mild petroleum-like odor. Liquid quickly evaporates and forms conbustible fumes. An odor threshold concentration of 20 ppmv was reported by Nagata and Takeuchi (1990).

Uses

2,2-Dimethylbutane is an acyclic alkane. Its Research Octane Number (RON) has been reported to be 91.8. It is used to Component of high-octane motor and aviation fuels, intermediate for agricultural chemicals.

Preparation

2,2-Dimethylbutane can be synthesised by the hydroisomerisation of 2,3-dimethylbutane using an acid catalyst.
By the thermal or catalytic union (alkylation) of ethylene and isobutane, both recovered from refinery gases.

Production Methods

2,2-Dimethylbutane is produced from crude oil, natural liquid gases, and petroleum refining processes.

Application

2,2-Dimethylbutane may be employed as probe to investigate the nature of possible active sites in supported metal catalysts.
Some of the reported applications of 2,2-dimethylbutane include:
Palladium-catalyzed radical oxidative alkoxycarbonylation to prepare various alkyl carboxylates.
Iridium-iron-catalyzed tandem dehydrogenation-isomerization-hydrosilylation to synthesize corresponding silane.

General Description

Colorless liquid with an odor of gasoline. Less dense than water and insoluble in water. Hence floats on water. Irritating vapor. Flash point -54°F.

Air & Water Reactions

Highly flammable. Insoluble in water.

Reactivity Profile

2,2-Dimethylbutane may be incompatible with strong oxidizing agents like nitric acid. Charring may occur followed by ignition of unreacted material and other nearby combustibles. In other settings, mostly unreactive. Not affected by aqueous solutions of acids, alkalis, most oxidizing agents, and most reducing agents. When heated sufficiently or when ignited in the presence of air, oxygen or strong oxidizing agents, burns exothermically to produce carbon dioxide and water.

Hazard

Highly flammable, dangerous fire and explosion risk, explosion limits 1.2–7%

Health Hazard

Inhalation causes dizziness, nausea, and vomiting; concentrated vapor may cause unconsciousness and collapse. Contact with liquid causes irritation of eyes; repeated contact may produce irritation of skin. Ingestion causes irritation of stomach. Aspiration causes severe lung irritation, rapidly developing pulmonary edema, and central nervous system excitement followed by depression.

Safety Profile

Probably an irritant and narcotic in high concentration. A very dangerous fire and explosion hazard when exposed to heat or flame; can react vigorously with oxidzing materials. Keep away from heat or open flame. To fight fire, use foam, CO2, dry chemical. When heated to decomposition it emits acrid smoke and irritating fumes.

Environmental Fate

Photolytic. Reported photooxidation rate constants for the reaction of 2,2-dimethylbutane with OH radicals at 297, 299, and 300 K are 2.59 x 10-12, 6.16 x 10-12, and 2.59 x 10-12 cm3/molecule?sec, respectively (Atkinson, 1985, 1990).
Chemical/Physical. Complete combustion in air yields carbon dioxide and water vapor. 2,2- Dimethylbutane will not hydrolyze because it has no hydrolyzable functional group.

Purification Methods

Distil it azeotropically with MeOH, then wash it with water, dry (Na2SO4) it, and distil it. [Beilstein 1 IV 367.]

110-54-3
96-14-0
107-83-5
75-83-2
79-29-8
Synthesis of 2,2-Dimethylbutane from Hexane
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View Lastest Price from 2,2-Dimethylbutane manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
2,2-Dimethylbutane pictures 2023-12-26 2,2-Dimethylbutane
75-83-2
US $100.00-1.00 / KG 1KG 99% g-kg-tons, free sample is available Henan Fengda Chemical Co., Ltd
2,2-Dimethylbutane pictures 2023-07-27 2,2-Dimethylbutane
75-83-2
US $1.10 / g 1g 99.0% Min 100 Tons Shaanxi Didu New Materials Co. Ltd
2,2-Dimethylbutane pictures 2020-01-13 2,2-Dimethylbutane
75-83-2
US $1.00 / g 1g Min98%HPLC g/kg/ton Career Henan Chemical Co
(CH3)3CCH2CH3 2,2-dimethyl-butan butane,2,2-dimethyl- NEOBUTANE 2,2-DIMETHYLBUTANE, STANDARD FOR GC 2,2-dinethyl butane neobutan (4-Heptoxyphenyl)-(4-heptoxyphenyl)imino-oxidoazanium Diazene, bis[4-(heptyloxy)phenyl]-, 1-oxide 2,2-Dimethylbutane,98% Ethyltrimethylmethane tert-Butylethane 2,2-Dimethylbutane,Neohexane 1,1,1,2-TetraMethylethane 2-Ethylisobutane 2,2-DiMethylbutane, 98% 100ML 3,3-DIMETHYLBUTANE 2,2-DIMETHYLBUTANE 2,2-DiMethylbutane, 98% 500ML 2,2-DiMethylbutane >=99.0% (GC) 2.2-DiMethylbu 2,2-Dimethylbutane> 2,2-Dimethylbutane ISO 9001:2015 REACH NEOHEXANE Trimethylpropane Pinacolborane Impurity 47 CA12726100 2,2-Dimethylbutane 75-83-2 H3C3CCH2CH3 75832 CH33CC2H5 CH3CH2CCH33 Building Blocks Analytical Standards Alkanes Analytical Chromatography Product Catalog Acyclic Alphabetic Organic Building Blocks DID - DIN Acyclic Alkanes Building Blocks Chemical Synthesis Organic Building Blocks Organics