N-Propyl iodide

Last updated
n-Propyl iodide; 1-Propyl iodide
1-Iodopropane.svg
N-propylIodide.png
Names
Preferred IUPAC name
1-Iodopropane [1]
Identifiers
3D model (JSmol)
505937
ChemSpider
ECHA InfoCard 100.003.147 OOjs UI icon edit-ltr-progressive.svg
EC Number
  • 203-460-2
PubChem CID
UNII
UN number 2392
  • InChI=1S/C3H7I/c1-2-3-4/h2-3H2,1H3 X mark.svgN
    Key: PVWOIHVRPOBWPI-UHFFFAOYSA-N X mark.svgN
  • CCCI
Properties
C3H7I
Molar mass 169.993 g·mol−1
AppearanceColorless liquid
Density 1.743
Melting point −101.40 °C; −150.52 °F; 171.75 K
Boiling point 101.6 to 103.2 °C; 214.8 to 217.7 °F; 374.7 to 376.3 K
1.1 g/L (at 20 °C)
Solubility in ethanol Miscible
Solubility in diethyl ether Miscible
Vapor pressure 5.733 kPa
1.2 μmol Pa−1 kg−1
1.5051
Viscosity 7.438 mPa (at 20 °C)
Thermochemistry
136.2 J K−1 mol−1
−687–−627 kJ mol−1
Hazards
GHS labelling:
GHS-pictogram-flamme.svg GHS-pictogram-exclam.svg
Warning
H226, H302, H315, H319, H332, H335
P261, P305+P351+P338
Flash point 44 °C (111 °F; 317 K)
Lethal dose or concentration (LD, LC):
  • 297 mg/kg (IP, mouse)
  • 300 mg/kg (IV, mouse)
  • 595 mg/kg (IP, guinea pig)
  • 650 mg/kg (IP, rat)
  • >1.8 g/kg (oral, mouse)
Safety data sheet (SDS) fishersci.com
Related compounds
Related iodoalkanes
Related compounds
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
X mark.svgN  verify  (what is  Yes check.svgYX mark.svgN ?)

n-Propyl iodide (also 1-propyl iodide or 1-iodopropane) is a colorless, flammable chemical compound. It has the chemical formula C3H7I and is prepared by heating n-propyl alcohol with iodine and phosphorus. [2]

Related Research Articles

An iodide ion is the ion I. Compounds with iodine in formal oxidation state −1 are called iodides. In everyday life, iodide is most commonly encountered as a component of iodized salt, which many governments mandate. Worldwide, iodine deficiency affects two billion people and is the leading preventable cause of intellectual disability.

In organic chemistry, a propyl group is a three-carbon alkyl substituent with chemical formula −CH2CH2CH3 for the linear form. This substituent form is obtained by removing one hydrogen atom attached to the terminal carbon of propane. A propyl substituent is often represented in organic chemistry with the symbol Pr.

<span class="mw-page-title-main">Lead(II) iodide</span> Chemical compound

Lead(II) iodide is a chemical compound with the formula PbI
2
. At room temperature, it is a bright yellow odorless crystalline solid, that becomes orange and red when heated. It was formerly called plumbous iodide.

<span class="mw-page-title-main">Propylparaben</span> Chemical compound

Propylparaben is the n-propyl ester of p-hydroxybenzoic acid. It occurs as a natural substance found in many plants and some insects. Additionally, it can be manufactured synthetically for use in cosmetics, pharmaceuticals, and foods. It is a member of the class of parabens and can be used as a preservative in many water-based cosmetics, such as creams, lotions, shampoos, and bath products. As a food additive, it has an E number, which is E216.

<span class="mw-page-title-main">Propyl acetate</span> Chemical compound

Propyl acetate, also known as propyl ethanoate, is an organic compound. Nearly 20,000 tons are produced annually for use as a solvent. This colorless liquid is known by its characteristic odor of pears. Due to this fact, it is commonly used in fragrances and as a flavor additive. It is formed by the esterification of acetic acid and propan-1-ol, often via Fischer–Speier esterification, with sulfuric acid as a catalyst and water produced as a byproduct.

<span class="mw-page-title-main">Thyroid peroxidase</span> Enzyme expressed mainly in the thyroid gland

Thyroid peroxidase, also called thyroperoxidase (TPO), thyroid specific peroxidase or iodide peroxidase, is an enzyme expressed mainly in the thyroid where it is secreted into colloid. Thyroid peroxidase oxidizes iodide ions to form iodine atoms for addition onto tyrosine residues on thyroglobulin for the production of thyroxine (T4) or triiodothyronine (T3), the thyroid hormones. In humans, thyroperoxidase is encoded by the TPO gene.

<span class="mw-page-title-main">3C-P</span> Chemical compound

3C-P (α-Methyl-4-propoxy-3,5-dimethoxyphenethylamine) is a psychedelic phenethylamine. It has structural and pharmacodynamic properties similar to the drugs mescaline, proscaline, and amphetamine. Little information exists on the human pharmacology of 3C-P, but a psychedelic dosage appears to be 20–40 mg, and is accompanied by stimulant and psychedelic effects such as visual enhancement and distortion. It can be synthesized from syringaldehyde by reaction with n-propyl iodide followed by condensation with nitroethane and reduction.

<span class="mw-page-title-main">1-Propanol</span> Primary alcohol compound

1-Propanol is a primary alcohol with the formula CH3CH2CH2OH and sometimes represented as PrOH or n-PrOH. It is a colourless liquid and an isomer of 2-propanol. It is formed naturally in small amounts during many fermentation processes and used as a solvent in the pharmaceutical industry, mainly for resins and cellulose esters, and, sometimes, as a disinfecting agent.

Acetyl iodide is an organoiodine compound with the formula CH3COI. It is a colourless liquid. It is formally derived from acetic acid. Although far rarer in the laboratory than the related acetyl bromide and acetyl chloride, acetyl iodide is produced, transiently at least, on a far larger scale than any other acid halide. Specifically, it is generated by the carbonylation of methyl iodide in the Cativa and Monsanto processes, which are the main industrial processes that generate acetic acid. It is also an intermediate in the production of acetic anhydride from methyl acetate.

<span class="mw-page-title-main">Magnesium iodide</span> Chemical compound

Magnesium iodide is an inorganic compound with the chemical formula MgI2. It forms various hydrates MgI2·xH2O. Magnesium iodide is a salt of magnesium and hydrogen iodide. These salts are typical ionic halides, being highly soluble in water.

<span class="mw-page-title-main">Isopropyl iodide</span> Chemical compound

Isopropyl iodide is the organoiodine compound with the formula (CH3)2CHI. It is colorless, flammable, and volatile. Organic iodides are light-sensitive and take on a yellow colour upon storage, owing to the formation of iodine.

Propyl iodide may refer to:

Iodopropane may refer to:

<span class="mw-page-title-main">Bismuth(III) iodide</span> Chemical compound

Bismuth(III) iodide is the inorganic compound with the formula BiI3. This gray-black salt is the product of the reaction of bismuth and iodine, which once was of interest in qualitative inorganic analysis.

Propyl propanoate (propyl propionate) is the organic compound with the molecular formula C6H12O2. It is the ester of propanol and propionic acid. Like most esters, propyl propanoate is a colorless liquid with a fruity odor. The scent of propyl propionate is described as a chemically tinged pineapple or pear. It is used in perfumery and as a solvent. The refractive index at 20 °C is 1.393.

Parisa Mehrkhodavandi is a Canadian chemist and Professor of Chemistry at the University of British Columbia (UBC). Her research focuses on the design of new catalysts that can effect polymerization of sustainably sourced or biodegradable polymers.

The molecular formula C3H7I (molar mass: 169.99 g/mol, exact mass: 169.9592 u) may refer to:

<span class="mw-page-title-main">Neodymium(II) iodide</span> Chemical compound

Neodymium(II) iodide or neodymium diiodide is an inorganic salt of iodine and neodymium the formula NdI2. Neodymium uses the +2 oxidation state in the compound.

<span class="mw-page-title-main">EA-1763</span> Chemical compound

EA-1763, O-PPVX, V1 or propyl S-2-diisopropylaminoethylmethylphosphonothiolate, is a military-grade neurotoxic organophosphonate nerve agent related to VX. It is part of the V-series. The substitution of a proton for methyl makes its properties more similar to those of VX.

<span class="mw-page-title-main">Ytterbium(II) iodide</span> Chemical compound

Ytterbium(II) iodide is an iodide of ytterbium, with the chemical formula of YbI2. It is a yellow solid.

References

  1. CID 33643 from PubChem
  2. Merck Index , 9th ed., monograph 7651