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1-Iodobutane

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CAS:542-69-8
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1-Iodobutane Basic information
Product Name:1-Iodobutane
Synonyms:1-Butyljodid;1-iodo-butan;1-Jodbutan;Butane,1-iodo-;Iodobutane;n-Butyliodid;n-C4H9I;1-IODOBUTANE , STABILIZED WITH COPPER
CAS:542-69-8
MF:C4H9I
MW:184.02
EINECS:208-824-4
Product Categories:Organics;Iodine Compounds
Mol File:542-69-8.mol
1-Iodobutane Structure
1-Iodobutane Chemical Properties
Melting point −103 °C(lit.)
Boiling point 130-131 °C(lit.)
density 1.617 g/mL at 25 °C(lit.)
vapor density ~5 (vs air)
vapor pressure 18.5 hPa (25 °C)
refractive index n20/D 1.498(lit.)
Fp 92 °F
storage temp. Store below +30°C.
solubility alcohol: soluble
form Liquid
color Clear colorless to pale yellow or light pink
Water Solubility Insoluble in water.
Sensitive Light Sensitive
Merck 14,1573
BRN 1420755
Dielectric constant4.5(130℃)
Stability:Stable. Highly flammable. Incompatible with strong oxidizing agents. Light sensitive.
InChI1S/C4H9I/c1-2-3-4-5/h2-4H2,1H3
InChIKeyKMGBZBJJOKUPIA-UHFFFAOYSA-N
SMILESCCCCI
CAS DataBase Reference542-69-8(CAS DataBase Reference)
NIST Chemistry ReferenceButane, 1-iodo-(542-69-8)
EPA Substance Registry SystemButane, 1-iodo- (542-69-8)
Safety Information
Hazard Codes Xn
Risk Statements 10-20-36/37/38-20/22
Safety Statements 16-36-36/37/39-26
RIDADR UN 1993 3/PG 3
WGK Germany 3
RTECS EK4400000
8
Hazard Note Harmful
TSCA TSCA listed
HazardClass 3
PackingGroup III
HS Code 29033080
Storage Class3 - Flammable liquids
Hazard ClassificationsAcute Tox. 3 Inhalation
Flam. Liq. 3
MSDS Information
ProviderLanguage
1-Iodobutane English
SigmaAldrich English
ACROS English
ALFA English
1-Iodobutane Usage And Synthesis
Chemical Propertiescolorless liquid. Soluble in chloroform, miscible with ethanol and ether, insoluble in water, and will change color when exposed to light or left for a long time.
Uses1-Iodobutane was used in the synthesis of S-alkylated 5-(2-,3- and 4-methoxyphenyl)-4H-1,2,4-triazole-3-thiol and 5-(2-,3- and 4-methoxyphenyl)-4-phenyl-4H-1,2,4-triazole-3-thiol. It is also used in wide range of medicals industrial applications as well as in human and animal nutrition products, pharmaceutical intermediates, polarizing films for Liquid Crystal Display (LCD) chemicals.
Preparation1-Iodobutane is obtained by reacting n-butanol with iodine in the presence of phosphorus.
Synthesis Reference(s)The Journal of Organic Chemistry, 44, p. 2048, 1979 DOI: 10.1021/jo01326a042
Synthesis, p. 114, 1976
General DescriptionThermal chemistry of 1-iodobutane has been investigated on clean and hydrogen- and deuterium-predosed Pt(111) single-crystal surfaces by temperature-programmed desorption and reflection-absorption infrared spectroscopy.
Purification MethodsDry the iodide with MgSO4 or P2O5, fractionally distil it through a column packed with glass helices, taking the middle fraction and storing over calcium or mercury in the dark. Alternatively purify it by prior passage through activated alumina or by shaking with conc H2SO4 then washing with Na2SO3 solution. It has also been treated carefully with sodium to remove free HI and H2O, before distilling through a column containing copper turnings at the top. Another purification procedure consisted of treatment with bromine, followed by extraction of free halogen with Na2S2O3, washing with H2O, drying and fractionally distilling. [Beilstein 1 IV 271.]
Tag:1-Iodobutane(542-69-8) Related Product Information
ISOBUTANE 1-Chlorobutane Iodine 2-Bromo-2-methylpropane BUTYL OLEATE Potassium iodide Cyhalofop-butyl Dibutyl phthalate n-Butane Buprofezin Propidium iodide 1-Chloro-2-methylpropane 1-Bromobutane 1,1,1,2,2,3,3,4,4-NONAFLUORO-4-IODOBUTANE,NONAFLUORO-1-IODOBUTANE,1,1,2,2,3,3,4,4,4-Nonafluoro-1-iodobutane,NONAFLUORO-1-IODOBUTANE, STAB. Perfluorooctyl iodide 1-Iodododecane 1-IODODECANE 1-IODOUNDECANE

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