2-iodopropane
propane, 2-iodo-
 
Notes:
None found
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CAS Number: 75-30-9Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg: 200-859-3
FDA UNII: 67K05OPZ0E
Nikkaji Web: J1.450H
Beilstein Number: 1098244
MDL: MFCD00001071
XlogP3-AA: 2.30 (est)
Molecular Weight: 169.99326000
Formula: C3 H7 I
NMR Predictor: Predict (works with chrome or firefox)
Category: pharmaceuticals / chemical synthisis
 
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Physical Properties:
Appearance: colorless to pale yellow clear liquid (est)
Assay: 95.00 to 100.00 % 
Food Chemicals Codex Listed: No
Specific Gravity: 1.70300 @  25.00 °C.
Melting Point: -90.00 °C. @ 760.00 mm Hg
Boiling Point: 89.50 °C. @ 760.00 mm Hg
Vapor Pressure: 61.431000 mmHg @ 25.00 °C. (est)
Flash Point: 108.00 °F. TCC ( 42.22 °C. )
logP (o/w): 2.890
Soluble in:
 water, 1400 mg/L @ 20 °C (exp)
 water, 209.3 mg/L @ 25 °C (est)
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Organoleptic Properties:
 
Odor and/or flavor descriptions from others (if found).
 
 
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Cosmetic Information:
None found
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Suppliers:
EMD Millipore
For experimental / research use only.
2-Iodopropane
Santa Cruz Biotechnology
For experimental / research use only.
2-Iodopropane
Sigma-Aldrich: Aldrich
For experimental / research use only.
2-Iodopropane contains copper as stabilizer, 99%
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Safety Information:
Preferred SDS: View
 
Hazards identification
 
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements
 
Pictogram
 
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
intraperitoneal-mouse LD50  1300 mg/kg
"Toxicology of Drugs and Chemicals," Deichmann, W.B., New York, Academic Press, Inc., 1969Vol. -, Pg. 756, 1969.

Dermal Toxicity:
Not determined
Inhalation Toxicity:
inhalation-rat LC50 320000 mg/m3/30M
Fiziologicheski Aktivnye Veshchestva. Physiologically Active Substances. Vol. 7, Pg. 35, 1975.

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Safety in Use Information:
Category: pharmaceuticals / chemical synthisis
Recommendation for 2-iodopropane usage levels up to:
 not for fragrance use.
 
Recommendation for 2-iodopropane flavor usage levels up to:
 not for flavor use.
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Safety References:
European Food Safety Authority (EFSA) reference(s):
Review of substances/agents that have direct beneficial effect on the environment: mode of action and assessment of efficacy
View page or View pdf
EPI System: View
Chemical Carcinogenesis Research Information System: Search
AIDS Citations: Search
Cancer Citations: Search
Toxicology Citations: Search
EPA Substance Registry Services (TSCA): 75-30-9
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 6362
National Institute of Allergy and Infectious Diseases: Data
WGK Germany: 3
 2-iodopropane
Chemidplus: 0000075309
RTECS: TZ4200000 for cas# 75-30-9
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References:
 2-iodopropane
NIST Chemistry WebBook: Search Inchi
Canada Domestic Sub. List: 75-30-9
Pubchem (cid): 6362
Pubchem (sid): 134970891
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Other Information:
(IUPAC): Atomic Weights of the Elements 2011 (pdf)
Videos: The Periodic Table of Videos
tgsc: Atomic Weights use for this web site
(IUPAC): Periodic Table of the Elements
HMDB (The Human Metabolome Database): Search
Export Tariff Code: 2903.30.2050
ChemSpider: View
Wikipedia: View
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Potential Blenders and core components note
 
None Found
 
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Potential Uses:
None Found
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Occurrence (nature, food, other): note
 not found in nature
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Synonyms:
2-iodo-propane
 propane, 2-iodo-
2-propyl iodide
sec-propyl iodide
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Articles:
PubMed: Coulomb repulsion versus cycloaddition: formation of anionic four-membered rings from sodium phosphaethynolate, Na(OCP).
PubMed: Unique structural properties of 2,4,6-tri-tert-butylanilide: isomerization and switching between separable amide rotamers through the reaction of anilide enolates.
PubMed: Carbodeoxygenation of biomass: the carbonylation of glycerol and higher polyols to monocarboxylic acids.
PubMed: Selective reduction of biomass by hydriodic acid and its in situ regeneration from iodine by metal/hydrogen.
PubMed: Development and validation of analytical procedure--control of residual 2-iodopropane in latanoprost.
PubMed: Dissociation dynamics of energy selected, propane, and i-C(3)H(7)X(+) Ions by iPEPICO: accurate heats of formation of i-C(3)H(7)(+), i-C(3)H(7)Cl, i-C(3)H(7)Br, and i-C(3)H(7)I.
PubMed: Diastereoselective addition of sugar radicals to camphorsultam glyoxilic oxime ether: a route toward C-glycosylthreonine and allothreonine.
PubMed: Flash pyrolysis of ethyl, n-propyl, and isopropyl iodides as monitored by supersonic expansion vacuum ultraviolet photoionization time-of-flight mass spectrometry.
PubMed: Density functional theory studies of negishi alkyl-alkyl cross-coupling reactions catalyzed by a methylterpyridyl-Ni(I) complex.
PubMed: Determination of spin-orbit branching fractions in the photodissociation of halogenated hydrocarbons.
PubMed: Rates and mechanisms for the reactions of chlorine atoms with iodoethane and 2-iodopropane.
PubMed: Interaction mechanism of some alkyl iodides with femtosecond laser pulses.
PubMed: Near-threshold photoionization of hot isopropyl radicals.
PubMed: Selective synthesis of [2-(11)C]2-iodopropane and [1-(11)C]iodoethane using the loop method by reacting methylmagnesium bromide with [11C]carbon dioxide.
PubMed: Inhibition of ruminal microbial methane production by beta-cyclodextrin iodopropane, malate and their combination in vitro.
PubMed: Alternative liquid chromatographic method for determination of the methoxyl and 2-hydroxypropoxyl content in cellulose ether derivatives.
PubMed: Formation of volatile iodinated alkanes in soil: results from laboratory studies.
PubMed: Synthesis and Reactivity of New 1,4-Bis(alkylthio)-3,6-diarylthieno[3,4-c]thiophene Derivatives.
PubMed: Synthesis of [isopropyl-11C]nimodipine for in vivo studies of dihydropyridine binding in man using positron emission tomography.
PubMed: Determination of diclofensine, an antidepressant agent, and its major metabolites in human plasma by high-performance liquid chromatography with fluorometric detection.
PubMed: Influence of corrinoid antagonists on methanogen metabolism.
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