2-Iodopropane supplier | CasNO.75-30-9

Name
Isopropyl iodide
EINECS 200-859-3
CAS No. 75-30-9
Article Data106
CAS DataBase
Density 1.747 g/cm³
Solubility
Melting Point -90 °C
Formula C₃H₇I
Boiling Point 91.3 °C at 760 mmHg
Molecular Weight 169.993
Flash Point 42.2 °C
Transport Information UN 2392 3/PG 3
Appearance Colorless liquid
Safety 36/37
Risk Codes 10-22
Molecular Structure
Hazard Symbols Xn
Synonyms 1-Methylethyliodide;2-Propyl iodide;Isopropyl iodide;sec-Propyl iodide;
PSA 0.00000
LogP 1.82980

Synthetic route

: 67-63-0
isopropyl alcohol

: 75-30-9
2-iodo-propane

Conditions

Conditions	Yield
With iodoform; sodium iodide In N,N-dimethyl-formamide for 3h; Catalytic behavior; Irradiation;	91%
With acetyl iodide at 80 - 90℃; for 1.5h;	24%
With iodine; aluminium

: 26591-86-6
(i-C3H7)3SbI2

A: 75-30-9
2-iodo-propane

B: 73300-45-5
tri(isopropyl)antimony

C: 81492-14-0
diisopropylantimony iodide

Conditions

Conditions	Yield
under Ar, decomposed at 135°C for 30 min; distd., not separated from triisopropyl stibine; elem. anal.;	A 89% B n/a C n/a

...Expand

: 420-26-8
2-propylfluoride

: 75-30-9
2-iodo-propane

Conditions

Conditions	Yield
With 2-fluoro-2-(piperidin-1-yl)-4-(2,3,5,6-tetrafluoropyridin-4-yl)-5-(2,4,6-triisopropylphenyl)-1,3-dithiole In 1,4-dioxane at 45℃; for 14h; Schlenk technique; Inert atmosphere;	74%

: 78-83-1
2-methyl-propan-1-ol

A: 75-30-9
2-iodo-propane

B: 78-84-2
isobutyraldehyde

Conditions

Conditions	Yield
With N-iodo-succinimide In chlorobenzene for 3h; Irradiation;	A 51% B 18%

: 74-98-6
propane

: 75-30-9
2-iodo-propane

Conditions

Conditions	Yield
With CCl4*2AlI3 In dichloromethane at -20℃; for 1.5h;	50%

: 137116-57-5
5'-O-(4,4'-dimethoxytrityl)-2-N-<2-<(tert-butyldiphenylsilyloxy)methyl>benzoyl>guanosine

: 18162-48-6
tert-butyldimethylsilyl chloride

A: 75-30-9
2-iodo-propane

B: 137116-54-2
5'-O-(4,4'-dimethoxytrityl)-3'-O-(tert-butyldimethylsilyl)-2-N-<2-<(tert-butyldiphenylsilyloxy)methyl>benzoyl>guanosine

Conditions

Conditions	Yield
With pyridine; silver nitrate In tetrahydrofuran	A 42% B 16%

...Expand

: 57-55-6
propylene glycol

: 75-30-9
2-iodo-propane

Conditions

Conditions	Yield
With water; hydrogen iodide

: 187737-37-7
propene

: 75-30-9
2-iodo-propane

Conditions

Conditions	Yield
With hydrogen iodide
With ascaridole; hydrogen iodide
With hydrogen iodide; diphenylamine
With hydrogen iodide

: 187737-37-7
propene

A: 75-30-9
2-iodo-propane

B: 107-08-4
1-iodo-propane

Conditions

Conditions	Yield
With hydrogen iodide; diphenylamine

: 556-56-9
allyl iodid

: 75-30-9
2-iodo-propane

Conditions

Conditions	Yield
With hydrogen iodide

: 29568-69-2
1,2-iodochloropropane

: 75-30-9
2-iodo-propane

Conditions

Conditions	Yield
With hydrogen iodide

: 108-20-3
di-isopropyl ether

: 75-30-9
2-iodo-propane

Conditions

Conditions	Yield
With phosphoric acid; potassium iodide
With diiodosilane In chloroform-d1 Ambient temperature; relative rates, other reagents, var. ethers;

: 2307-69-9
toluene-4-sulfonic acid isopropyl ester

: 75-30-9
2-iodo-propane

Conditions

Conditions	Yield
With water; potassium iodide

: 107-08-4
1-iodo-propane

A: 75-30-9
2-iodo-propane

B: 75-03-6
ethyl iodide

C: 74-88-4
methyl iodide

Conditions

Conditions	Yield
mit UV-Licht (253.7 nm),in fluess. Zustand;bei Abwesenheit von Sauerstoff.Irradiation;

...Expand

: 56-81-5
glycerol

: 75-30-9
2-iodo-propane

Conditions

Conditions	Yield
With phosphorus; water; iodine und nachfolgendes Dastillieren des Reaktionsprodukts;
With water; hydrogen iodide
With phosphorous; water; iodine
With hydrogen iodide In water; benzene at 100℃; under 15514.9 Torr; for 16h; Inert atmosphere; Autoclave;	100 %Chromat.

: 75-26-3
isopropyl bromide

: 75-30-9
2-iodo-propane

Conditions

Conditions	Yield
With pyridine; tributyltin iodide at 125℃; Thermodynamic data; Equilibrium constant; Δ G;
With sodium iodide In acetone at 55℃; Kinetics; quantitative reaction kinetics in liquid state by in situ X-ray absorption fine structure spectroscopy;
With acetone; sodium iodide

: 116-17-6
triisopropyl phosphite

: 74-88-4
methyl iodide

A: 75-30-9
2-iodo-propane

B: 1445-75-6
diisopropyl methanephosphonate

Conditions

Conditions	Yield
reagiert analog mit Brom-diphenyl-p-biphenylyl-methan und Homologen;

...Expand

: 2916-31-6
2,2-dimethyl-1,3-dioxolane

: 75-30-9
2-iodo-propane

Conditions

Conditions	Yield
With diiodosilane In chloroform-d1 at 22℃; for 4h;	99 % Spectr.

: 556-56-9
allyl iodid

: 593-71-5
Chloroiodomethane

: 1068-55-9
isopropylmagnesium chloride

A: 75-30-9
2-iodo-propane

B: 513-38-2
Isobutyl iodide

C: 7766-51-0
4-iodobut-1-ene

Conditions

Conditions	Yield
In tetrahydrofuran; diethyl ether at -40℃; for 4.5h; Product distribution;
In tetrahydrofuran at -40℃; for 4.5h;

...Expand

: 76509-66-5
diisopropyl ethylphosphonite

: 754-34-7
1,1,1,2,2,3,3-heptafluoro-3-iodo-propane

A: 75-30-9
2-iodo-propane

B: 77529-57-8
isopropyl ethyl(heptafluoropropyl)phosphinate

Conditions

Conditions	Yield
In octane Rate constant; Kinetics; Thermodynamic data; E (activ.); ΔH(excit.); ΔS(excit.); ΔG(excit.);

...Expand

: 187737-37-7
propene

: 64-19-7
acetic acid

A: 75-30-9
2-iodo-propane

B: 108-21-4
Isopropyl acetate

C: 67-63-0
isopropyl alcohol

Conditions

Conditions	Yield
With carbon monoxide; water; hydrogen iodide; TsVK-2; palladium at 110℃; under 60800 Torr; for 2h; Product distribution; further temperature (130 deg C);

...Expand

: 77-76-9
2,2-dimethoxy-propane

: 75-30-9
2-iodo-propane

Conditions

Conditions	Yield
With diiodosilane; iodine 1.) CDCl3, 22 deg C, 10 min, 2.) 30 min; Yield given. Multistep reaction;

: 67-64-1
acetone

: 75-30-9
2-iodo-propane

Conditions

Conditions	Yield
With diiodosilane; iodine In chloroform-d1 at 22℃; for 3h;	100 % Spectr.

: 67-64-1
acetone

A: 75-30-9
2-iodo-propane

B: 108-20-3
di-isopropyl ether

Conditions

Conditions	Yield
With diiodosilane In chloroform-d1 for 0.166667h; Ambient temperature; other reaction time: 80 min, effect of iodine; Yield given. Further byproducts given. Yields of byproduct given. Title compound not separated from byproducts;

: 187737-37-7
propene

: 201230-82-2
carbon monoxide

: 79-31-2
isobutyric Acid

A: 75-30-9
2-iodo-propane

B: 617-50-5
isopropyl isobutyrate

C: 638-11-9
isopropyl butyrate

D: 67-63-0
isopropyl alcohol

E: 107-92-6
butyric acid

Conditions

Conditions	Yield
With water; hydrogen iodide; TsVK-2; palladium at 130℃; under 60800 Torr; for 2h; Product distribution; further temperature (110, 150, 170, 200 deg C); effect of the concentration of HI; effect of the pressure of CO;

...Expand

: 2025-55-0
isopropyl radical

: 74-88-4
methyl iodide

A: 75-30-9
2-iodo-propane

B: 2229-07-4
methyl radical

Conditions

Conditions	Yield
Equilibrium constant;

...Expand

: C3H7I(1+)*CCl4*Cl(1-)

: 108-95-2
phenol

A: 75-30-9
2-iodo-propane

B: 56-23-5
tetrachloromethane

C: 2122-46-5, 55748-05-5
phenoxy radical

Conditions

Conditions	Yield
In tetrachloromethane at 22℃; Rate constant; multistep reaction;

...Expand

: 108-21-4
Isopropyl acetate

: 75-30-9
2-iodo-propane

Conditions

Conditions	Yield
With trimethylsilyl iodide; bismuth(III) iodide In neat (no solvent) at 80℃; for 0.25h;	98 % Chromat.

: 626-67-5
N-methylcyclohexylamine

: 75-30-9
2-iodo-propane

: 84437-36-5
1-isopropyl-1-methyl-piperidinium; iodide

Conditions

Conditions	Yield
In chloroform at 60℃; for 8h;	100%
In chloroform Heating;

: 75-30-9
2-iodo-propane

: 5597-27-3
3-methylenebicyclo[2.2.1]heptan-2-one

: 108350-17-0
3-isobutylbicyclo<2.2.1>heptan-2-one

Conditions

Conditions	Yield
With copper(l) iodide; zinc In water Product distribution; further solvent: aq. ethanol, further activators: ammonium formate, ammonium chloride; ultrasonic irradiation;	100%
With copper(l) iodide; zinc In water ultrasonic irradiation;	100%

: 75-30-9
2-iodo-propane

: 481-39-0
5-hydroxynaphtho-1,4-quinone

: 97308-90-2
5-isopropoxy-1,4-naphthoquinone

Conditions

Conditions	Yield
With silver(l) oxide In dichloromethane at 20℃; for 20h; Green chemistry; regioselective reaction;	100%
With silver(l) oxide In chloroform for 0.333333h; Ambient temperature;	77%

: 75-30-9
2-iodo-propane

: C10H21N4PS2

: 1-Isopropylsulfanylthiocarbonyl-2,8,9-trimethyl-2,5,8,9-tetraaza-1-phosphonia-bicyclo[3.3.3]undecane; iodide

Conditions

Conditions	Yield
In acetonitrile for 43h;	100%

: 75-30-9
2-iodo-propane

: 119289-79-1
3-(4-hydroxy-2-nitrophenyl)pyridine

: 158461-41-7
3-(4-isopropoxy-2-nitrophenyl)pyridine

Conditions

Conditions	Yield
With potassium carbonate In N,N-dimethyl-formamide at 40℃; for 6h;	100%

: 75-30-9
2-iodo-propane

: 491-35-0
C6H4NCH2CHCCH2

: 91879-71-9
2-isopropyl-4-methylquinoline

Conditions

Conditions	Yield
With sodium azide; [bis(acetoxy)iodo]benzene; trifluoroacetic acid In isopropyl alcohol Product distribution; various solvents;	100%
With sodium azide; [bis(acetoxy)iodo]benzene; trifluoroacetic acid In isopropyl alcohol Heating;	100%
With tert.-butylhydroperoxide; acetic acid ; ferriacetate; trifluoroacetic acid In acetic acid for 4h; Heating;	92%

: 75-30-9
2-iodo-propane

: 101-41-7
benzeneacetic acid methyl ester

: 72615-27-1
2-phenyl-3-methylbutyric acid methyl ester

Conditions

Conditions	Yield
With N,N,N,N,N,N-hexamethylphosphoric triamide; lithium diisopropyl amide In tetrahydrofuran at -78℃;	100%
With 2-pyrrolidinon In N,N-dimethyl-formamide Flow reactor;	16%
With 1) EGB.2 1) -78 deg C, 2) -78 deg C, 15 min; Yield given. Multistep reaction;

: 75-30-9
2-iodo-propane

: 159647-63-9
3-(2,3-Dihydro-benzo[1,4]dioxin-6-yl)-2,6-diethyl-7-hydroxy-chromen-4-one

: 3-(2,3-Dihydro-benzo[1,4]dioxin-6-yl)-2,6-diethyl-7-isopropoxy-chromen-4-one

Conditions

Conditions	Yield
With potassium carbonate In acetone for 34.5h; Heating;	100%
With potassium carbonate In acetone Heating;	99.8%

: 75-30-9
2-iodo-propane

: 371-42-6
4-Fluorothiophenol

: 702-13-6
1-Fluoro-4-(isopropylthio)benzene

Conditions

Conditions	Yield
With potassium carbonate In N,N-dimethyl-formamide at 60℃;	100%

: 75-30-9
2-iodo-propane

: 699-18-3, 32782-45-9
2-[(E)-2-nitroethenyl]furan

: 20992-64-7
(E)-1-(2-furyl)-3-methyl-1-butene

Conditions

Conditions	Yield
With triethylaluminum; dibenzoyl peroxide In diethyl ether at 20℃; for 2h;	100%
With air; triethyl borane In tetrahydrofuran at 20℃;	100%

: 75-30-9
2-iodo-propane

: 34312-77-1
1-(2-thienyl)-2-nitroethene

: (E)-3-methyl-1-(2-thienyl)-1-butene

Conditions

Conditions	Yield
With air; triethyl borane In tetrahydrofuran at 20℃;	100%
With triethylaluminum; dibenzoyl peroxide In diethyl ether at 20℃; for 2h;	98%

: 75-30-9
2-iodo-propane

: 3179-10-0, 5576-97-6
(E)-1-methoxy-4-(2-nitrovinyl)benzene

: 103786-20-5
(E)-1-methoxy-4-(3-methyl-but-1-en-1-yl)benzene

Conditions

Conditions	Yield
With triethyl borane; oxygen In tetrahydrofuran at 20℃;	100%
With triethylaluminum; dibenzoyl peroxide In diethyl ether at 20℃; for 2h;	99%
With triethyl borane In diethyl ether; water
With triethyl borane In tetrahydrofuran at 20℃;

: 75-30-9
2-iodo-propane

: 101671-01-6
1-nitro-2-(4-chlorophenyl)ethylene

: (E)-1-chloro-4-(3-methylbut-1-en-1-yl)benzene

Conditions

Conditions	Yield
With triethylaluminum; dibenzoyl peroxide In diethyl ether at 20℃; for 2h;	100%
With air; triethyl borane In tetrahydrofuran at 20℃;	98%

: 75-30-9
2-iodo-propane

: 17851-98-8
1-phenyl-1-(tributylstannyloxy)ethene

: 624-49-7
dimethylfumarate

: dimethyl 2-isopropyl-3-phenacylbutanedioate

Conditions

Conditions	Yield
With 2,2'-azobis(isobutyronitrile) In benzene at 80℃; for 4h;	100%

...Expand

: 75-30-9
2-iodo-propane

: 5535-48-8
PVS

: 52075-20-4
1-phenylsulphonyl-3-methyl butane

Conditions

Conditions	Yield
With hydrogenchloride; water; sodium chloride In acetonitrile for 20h; pH=2; Solvent; pH-value; Electrochemical reaction; Green chemistry;	100%
With 2,2'-azobis(isobutyronitrile); tert-butyl(2,6-dimethoxy-1-methylcyclohexa-2,5-dien-1-yl)dimethylsilane In hexane for 14h; Giese-type addition; Heating;	89%
With indium In methanol; water at 20℃; for 0.5h;	86%

: 75-30-9
2-iodo-propane

: (S)-4-Benzyloxy-2-methylene-undecanoic acid cyclohexyl ester

: (2S,4S)-4-Benzyloxy-2-isobutyl-undecanoic acid cyclohexyl ester

Conditions

Conditions	Yield
With triethyl borane; tri-n-butyl-tin hydride; magnesium bromide In hexane; dichloromethane at 0℃; for 1h;	100%

: 75-30-9
2-iodo-propane

: 401819-62-3
4-(7-hydroxy-6-methoxy-4-quinazolinyl)-1-piperazinecarboxylic acid tert-butyl ester

: 205259-43-4
4-(7-isopropoxy-6-methoxy-4-quinazolinyl)-1-piperazinecarboxylic acid tert-butyl ester

Conditions

Conditions	Yield
With potassium carbonate In N,N-dimethyl-formamide at 20℃;	100%

: 75-30-9
2-iodo-propane

: 63435-16-5
3-hydroxy-4-aminobenzoic acid methyl ester

: 681465-85-0
4-amino-3-isopropoxybenzoic acid methyl ester

Conditions

Conditions	Yield
With caesium carbonate In acetone at 60℃; for 2h; Inert atmosphere;	100%
With caesium carbonate In acetone for 10h; Heating;	90%
With caesium carbonate In acetone for 10h; Heating / reflux;	90%
With caesium carbonate In acetone at 120℃; for 1h; Microwave;	60%
With caesium carbonate In acetone

: 75-30-9
2-iodo-propane

: 1439-36-7
1-triphenylphosphoranylidene-2-propanone

: 27653-95-8
4-methyl-1-(triphenylphosphaneylidene)pentan-2-one

Conditions

Conditions	Yield
Stage #1: 1-triphenylphosphoranylidene-2-propanone With n-butyllithium In tetrahydrofuran; hexane at -78℃; for 1h; Stage #2: 2-iodo-propane In tetrahydrofuran; hexane at -78 - 20℃;	100%

: 75-30-9
2-iodo-propane

: 49543-63-7
4-tert-butylbenzyl mercaptan

: 1-tert-butyl-4-isopropylsulfanylmethyl-benzene

Conditions

Conditions	Yield
Stage #1: 4-tert-butylbenzyl mercaptan With tetra-(n-butyl)ammonium iodide; caesium carbonate In N,N-dimethyl-formamide at 20℃; for 1h; Stage #2: 2-iodo-propane In N,N-dimethyl-formamide at 0 - 20℃; for 18h;	100%

: 75-30-9
2-iodo-propane

: 86-73-7
9H-fluorene

: 3299-99-8
9-isopropyl-9H-fluorene

Conditions

Conditions	Yield
Stage #1: 9H-fluorene With n-butyllithium In tetrahydrofuran; hexane at 20℃; for 1.5h; Stage #2: 2-iodo-propane In tetrahydrofuran; hexane at 20℃; for 2h; Further stages.;	100%
Stage #1: 9H-fluorene With n-butyllithium; diisopropylamine In tetrahydrofuran; hexane at -15℃; for 0.333333h; Stage #2: 2-iodo-propane In tetrahydrofuran; hexane at -15℃; for 0.5h; Further stages.;
With lithium diisopropyl amide In tetrahydrofuran at -10℃;

: 75-30-9
2-iodo-propane

: 70768-92-2
5,6-bis(4-methoxyphenyl)-2H-pyridazin-3-one

: 5,6-bis(4-methoxyphenyl)-2-isopropyl-2H-pyridazin-3-one

Conditions

Conditions	Yield
	100%

: 308386-35-8
1,1-dimethylethyl 4-(4'-pyridinyloxy)-1-piperidinecarboxylate

: 75-30-9
2-iodo-propane

: 845305-79-5
4-[(1-{tert-butoxycarbonyl}-4-piperidinyl)oxy]-1-(1-methylethyl)pyridinium iodide

Conditions

Conditions	Yield
In dichloromethane at 20℃;	100%
In dichloromethane at 90℃; for 2.5 - 48h;

: 75-30-9
2-iodo-propane

: 156001-68-2
methyl 3-cyano-4-hydroxybenzoate

: 213598-11-9
3-cyano-4-isopropoxybenzoic acid methyl ester

Conditions

Conditions	Yield
With potassium carbonate In DMF (N,N-dimethyl-formamide) at 50℃; for 16h;	100%
With potassium carbonate In N,N-dimethyl-formamide at 50℃; for 16h;	100%
With potassium carbonate In N,N-dimethyl-formamide at 90℃; for 12h; Inert atmosphere;

: 75-30-9
2-iodo-propane

: 123148-78-7
4-chloro-5-iodo-7H-pyrrolo[2,3-d]pyrimidine

: 213744-81-1
4-chloro-5-iodo-7-isopropyl-7H-pyrrolo[2,3-d]pyrimidine

Conditions

Conditions	Yield
Stage #1: 4-chloro-5-iodo-7H-pyrrolo[2,3-d]pyrimidine With caesium carbonate In N,N-dimethyl-formamide at 20℃; for 0.05h; Stage #2: 2-iodo-propane	100%
In N,N-dimethyl-formamide

: 75-30-9
2-iodo-propane

: 194237-29-1
5-(1-methyl-6-trifluoromethyl-2(1H)-pyridon-3-yl)-2-chloro-4-fluorobenzoic acid

: 194236-57-2
isopropyl 5-(1-methyl-6-trifluoromethyl-2(1H)-pyridon-3-yl)-2-chloro-4-fluorobenzoate

Conditions

Conditions	Yield
With potassium carbonate In N,N-dimethyl-formamide	100%

: 75-30-9
2-iodo-propane

: 344331-90-4
tert-butyl 6-bromopyridin-2-ylcarbamate

: 884539-05-3
tert-butyl N-(6-bromo-2-pyridyl)-N-isopropylcarbamate

Conditions

Conditions	Yield
With sodium hydride In N,N-dimethyl-formamide at 0 - 20℃; for 25.5h;	100%

: 75-30-9
2-iodo-propane

: 914397-24-3
7-benzyloxy-6-bromo-2-isopropylaminoquinazoline

Conditions

Conditions	Yield
Stage #1: 7-benzyloxy-6-bromo-2-aminoquinazoline With sodium hydride In N,N-dimethyl-formamide at 5℃; for 0.5h; Stage #2: 2-iodo-propane In N,N-dimethyl-formamide at 60℃; for 1.5h; Stage #3: 2-iodo-propane With sodium hydride Product distribution / selectivity; more than 3 stages;	100%

: 75-30-9
2-iodo-propane

: 580-20-1
quinolin-7-ol

: 1011533-28-0
C12H13NO

Conditions

Conditions	Yield
With caesium carbonate In N,N-dimethyl-formamide	100%

: 75-30-9
2-iodo-propane

: (C5H5)3U(CH(CH3)2)(1-)

: triscyclopentadienyl uranium(IV)-(i-C3H7)

Conditions

Conditions	Yield
In tetrahydrofuran-d8 byproducts: I(1-); react. in a glove box under Ar at 20°C, addn. of the organic halide via syringe to a soln. of Cp3UiPr(1-) in THF-d8, react. time: 10 min; determination by 1H NMR spectroscopy;	100%

2-Iodopropane Chemical Properties

The Molecular formula of ISOPROPYL IODIDE(75-30-9): C₃H₇I
The Molecular Weight of ISOPROPYL IODIDE(75-30-9): 169.99
The Molecular Structure of ISOPROPYL IODIDE(75-30-9):

EINECS: 200-859-3
Melting point: -90 °C
Boiling Point: 91.3 °C at 760 mmHg
Flash Point: 42.2 °C
Index of Refraction: 1.505
Molar Refractivity: 28.87 cm³
Molar Volume: 97.2 cm³
Polarizability: 11.44 10^-24 cm³
Surface Tension: 27.5 dyne/cm
Density: 1.747 g/cm³
Enthalpy of Vaporization: 30.68 kJ/mol
Vapour Pressure: 61.4 mmHg at 25°C
storage temp.: Store at RT.
Sensitive: Light Sensitive
Stability: Stable, but may discolour on exposure to light. Air sensitive. Incompatible with strong bases, strong oxidizing agents.
Appearance: Colorless liquid
Merck: 14,5214
BRN: 1098244
IUPAC Name: 2-iodopropane
Synonyms: 2-iodo-propan;2-Propyljodid;Isopropyl iodine;Isopropyliodid;i-Propyl iodide;iso-C₃H₇I;2-Jodpropan;2-propyliodide;

2-Iodopropane Uses

ISOPROPYL IODIDE(75-30-9) is used as a solvent, also used in medicine and organic synthesis.

2-Iodopropane Toxicity Data With Reference

The Toxicity Information of ISOPROPYL IODIDE(75-30-9):

1.		ihl-rat LC50:320,000 mg/m3/30M		FAVUAI Fiziologicheski Aktivnye Veshchestva. Physiologically Active Substances. 7 (1975),35.
2.		ipr-mus LD50:1300 mg/kg		34ZIAG Toxicology of Drugs and Chemicals ,Deichmann, W.B.,New York, NY.: Academic Press, Inc.,1969,756.

2-Iodopropane Consensus Reports

Reported in EPA TSCA Inventory.

2-Iodopropane Safety Profile

Moderately toxic by intraperitoneal route. Mildly toxic by inhalation. Questionable carcinogen with experimental neoplastigenic data. When heated to decomposition it emits toxic fumes of I⁻. See also IODIDES.
The Hazard Codes of ISOPROPYL IODIDE(75-30-9):

Xn
HazardClass: 3
The Risk Statements information of ISOPROPYL IODIDE(75-30-9):
10: Flammable
22: Harmful if swallowed
The Safety Statements information of ISOPROPYL IODIDE(75-30-9):
36/37: Wear suitable protective clothing and gloves
RIDADR: UN 2392 3/PG 3
WGK Germany: 3
RTECS: TZ4200000
F: 8
PackingGroup: III

Product Name

Isopropyl iodide

Synthetic route

2-Iodopropane Chemical Properties

2-Iodopropane Uses

2-Iodopropane Toxicity Data With Reference

2-Iodopropane Consensus Reports

2-Iodopropane Safety Profile

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