1-Iodobutane supplier | CasNO.542-69-8

Name
1-Iodobutane
EINECS 208-824-4
CAS No. 542-69-8
Article Data120
CAS DataBase
Density 1.622 g/cm³
Solubility Insoluble in water.
Melting Point -103 °C(lit.)
Formula C₄H₉I
Boiling Point 130.9 °C at 760 mmHg
Molecular Weight 184.02
Flash Point 33.3 °C
Transport Information UN 1993 3/PG 3
Appearance liquid
Safety 16-36-36/37/39-26
Risk Codes 10-20-36/37/38-20/22
Molecular Structure
Hazard Symbols Xn
Synonyms Butyl iodide;1-Iodobutane Butyl iodide;1-Butyliodide;Butane,1-iodo-;1-Jodbutan [Czech];
PSA 0.00000
LogP 2.22150

Synthetic route

: 71-36-3
butan-1-ol

: 542-69-8
1-iodo-butane

Conditions

Conditions	Yield
With potassium iodide In acetonitrile at 20℃; for 0.25h;	95%
With iodine; triphenylphosphine at 20℃; for 0.133333h; Ionic liquid;	91%
With hydrogen iodide at 120℃; for 4h;	80%

: 71-41-0
pentan-1-ol

A: 96-47-9
2-methyltetrahydrofuran

B: 542-69-8
1-iodo-butane

C: 110-62-3
pentanal

Conditions

Conditions	Yield
With N-iodo-succinimide In chlorobenzene for 2h; Irradiation;	A 94% B 1% C n/a
With N-iodo-succinimide In chlorobenzene for 2h; Product distribution; Irradiation; var. irradiat. times, temps. and light cond.;	A 94% B 1% C n/a

...Expand

: 142-96-1
dibutyl ether

: 542-69-8
1-iodo-butane

Conditions

Conditions	Yield
With hexaethylbisphosphonium bistriiodide Heating;	88%
With phosphoric acid; potassium iodide

: 1743-56-2
N-isobutylideneethylamine

: 59611-99-3
dibutyl phosphoriodidite

A: 542-69-8
1-iodo-butane

B: 2-butoxy-1,4-diethyl-3,5-diisopropyl-1,4,2-diazaphospholidine 2-oxide

Conditions

Conditions	Yield
In diethyl ether for 2h; Ambient temperature;	A n/a B 85%

...Expand

: 109-65-9
1-bromo-butane

: 542-69-8
1-iodo-butane

Conditions

Conditions	Yield
With I*2H2O In toluene at 150℃; Rate constant;	80%
With I*2H2O In toluene at 150℃;	80%
With sodium iodide In acetone Substitution;	64%

: n-Butyldiphenylsulfoniumperchlorat

: 542-69-8
1-iodo-butane

Conditions

Conditions	Yield
With potassium iodide In dichloromethane; water at 20℃; for 0.15h;	78%
With potassium iodide In dichloromethane; water at 20℃; for 0.15h; Product distribution; further diphenylalkylsulfonium salts, further K salts and other nucleophiles;	78%

: 311-28-4
tetra-(n-butyl)ammonium iodide

A: 542-69-8
1-iodo-butane

B: 102-82-9
tributyl-amine

Conditions

Conditions	Yield
With tetrabutylammonium tetrafluoroborate In acetone at 320℃; Product distribution; in a gas chromatograph; other temperature; various concentration of reagent;	A 77% B n/a

: 102-82-9
tributyl-amine

: 542-69-8
1-iodo-butane

Conditions

Conditions	Yield
With 2-chloro-4,6-dimethoxy-1 ,3,5-triazine; sodium iodide In acetone Reflux;	70%

: 111-34-2
-butyl vinyl ether

: 507-02-8
acetyl iodide

A: 108-05-4
vinyl acetate

B: 542-69-8
1-iodo-butane

C: 593-66-8
vinyliodide

D: 123-86-4
acetic acid butyl ester

Conditions

Conditions	Yield
In dichloromethane at 10℃;	A 11.8% B 12.8% C 35.8% D 39.8%

...Expand

: 109-69-3
n-Butyl chloride

: 542-69-8
1-iodo-butane

Conditions

Conditions	Yield
With iron pentacarbonyl; iodoform In N,N-dimethyl-formamide 1.) 70-90 deg C, 1 h, 2.) 80-90, 1 h;	37%
With ethylene glycol; potassium iodide
With iodine; iron pentacarbonyl at 85 - 90℃; for 1.5h; further reagent; Yield given;

: 106-97-8
n-butane

A: 542-69-8
1-iodo-butane

B: 513-48-4, 52152-71-3
2-butyl iodide

Conditions

Conditions	Yield
With tert-butylhypochlorite; mercury(II) iodide In 1,1,2-Trichloro-1,2,2-trifluoroethane at 47℃; for 8h; Irradiation; Yield given;	A n/a B 35%
With tert-butylhypochlorite; mercury(II) iodide In 1,1,2-Trichloro-1,2,2-trifluoroethane at 47℃; for 8h; Irradiation;	A n/a B 35%

: 109-72-8, 29786-93-4
n-butyllithium

: 75-11-6
diiodomethane

: (1Z)-N-(3-ethynylphenyl)-2,2,2-trifluoroethanimidoyl chloride

A: 542-69-8
1-iodo-butane

B: N,N'-[(2Z,4Z)-1,1,1,5,5,5-hexafluoro-2-penten-2-yl-4-ylidene]bis(3-ethynylaniline)

Conditions

Conditions	Yield
Stage #1: diiodomethane; (1Z)-N-(3-ethynylphenyl)-2,2,2-trifluoroethanimidoyl chloride With methyllithium lithium bromide In tetrahydrofuran; diethyl ether at -78℃; for 0.5h; Stage #2: n-butyllithium In tetrahydrofuran; diethyl ether; hexane at -78℃; for 0.5h;	A 25% B 31%

...Expand

: 109-99-9
tetrahydrofuran

: 542-69-8
1-iodo-butane

Conditions

Conditions	Yield
With phosphoric acid; potassium iodide

: 1809-19-4
dibutyl hydrogen phosphite

A: 542-69-8
1-iodo-butane

B: 16456-56-7
Phosphoric acid mono-n-butylester

Conditions

Conditions	Yield
With hydrogen iodide

: 778-28-9
butyl para-toluenesulfonate

: 542-69-8
1-iodo-butane

Conditions

Conditions	Yield
With water; potassium iodide
With tetra-(n-butyl)ammonium iodide In acetone at 210℃; Product distribution; ina gas chromatograph;

: 628-28-4
butyl methyl ether

: 191340-22-4
chloro-acetyl iodide

A: 590-02-3
butyl chloroacetate

B: 542-69-8
1-iodo-butane

C: 74-88-4
methyl iodide

...Expand

: 142-96-1
dibutyl ether

: 507-02-8
acetyl iodide

A: 542-69-8
1-iodo-butane

B: 123-86-4
acetic acid butyl ester

Conditions

Conditions	Yield
at 25℃; unter Lichtausschluss;

...Expand

: 142-96-1
dibutyl ether

: 70116-77-7
butyl 2,4,6-trimethylbenzoate

: 16002-63-4
phenylmagnesium iodide

A: 542-69-8
1-iodo-butane

B: 92-52-4
biphenyl

C: 480-63-7
mesitylenecarboxylic acid

Conditions

Conditions	Yield
anschliessend Behandeln mit wss. Schwefelsaeure;

...Expand

: 65039-16-9
1-butyl-3-propyl-imidazolium; iodide

A: 35203-44-2
1-propyl-1H-imidazole

B: 4316-42-1
1-Butylimidazole

C: 542-69-8
1-iodo-butane

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

Conditions

Conditions	Yield
at 260 - 300℃; im Vakuum;

...Expand

: 109-72-8, 29786-93-4
n-butyllithium

: 75-03-6
ethyl iodide

A: 542-69-8
1-iodo-butane

B: 811-49-4
ethyllithium

Conditions

Conditions	Yield
reversible Reaktion;

...Expand

: 74-85-1
ethene

: 75-03-6
ethyl iodide

: 542-69-8
1-iodo-butane

Conditions

Conditions	Yield
With water; dibenzoyl peroxide at 95℃; unter hohem Druck;

: 65039-17-0
3-ethyl-1-butyl-imidazolium; iodide

A: 7098-07-9
N-Ethylimidazole

B: 4316-42-1
1-Butylimidazole

C: 542-69-8
1-iodo-butane

D: 75-03-6
ethyl iodide

Conditions

Conditions	Yield
at 260 - 300℃; im Vakuum;

...Expand

: 109-65-9
1-bromo-butane

: 4206-67-1
iodo(trimethylsilyl)methane

A: 542-69-8
1-iodo-butane

B: 18243-41-9
(bromomethyl)trimethylsilane

Conditions

Conditions	Yield
With triisooctyl amine Equilibrium constant;

...Expand

: 106-98-9
1-butylene

: 542-69-8
1-iodo-butane

Conditions

Conditions	Yield
With borane; iodine; sodium methylate 1.) THF, 25 deg C, 1 h, 2.) MeOH, 24 h; Yield given. Multistep reaction;

: 628-21-7
1,4-Diiodobutane

A: 542-69-8
1-iodo-butane

B: 74-85-1
ethene

Conditions

Conditions	Yield
With sodium hydroxide; nickel tetraaza macrocycle; water at 25℃;

: 109-72-8, 29786-93-4
n-butyllithium

: 542-69-8
1-iodo-butane

Conditions

Conditions	Yield
With tri-n-butylstannylmethyl iodide

: 590-18-1
(Z)-2-Butene

: 542-69-8
1-iodo-butane

Conditions

Conditions	Yield
With borane; iodine; sodium methylate 1.) THF, 25 deg C, 1 h, 2.) MeOH, 24 h; Yield given. Multistep reaction;

: 109-69-3
n-Butyl chloride

: 4206-67-1
iodo(trimethylsilyl)methane

A: 542-69-8
1-iodo-butane

B: 2344-80-1
Chloromethyltrimethylsilane

Conditions

Conditions	Yield
With triisooctyl amine Equilibrium constant;

...Expand

: 24603-81-4
dibutyl ethylphosphonite

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

A: 542-69-8
1-iodo-butane

B: 77529-58-9
butyl ethyl(heptafluoropropyl)phosphinate

Conditions

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

...Expand

: 542-69-8
1-iodo-butane

: 106-97-8
n-butane

Conditions

Conditions	Yield
With lithium aluminium tetrahydride In tetrahydrofuran at 25℃; for 1h; Product distribution; var. aralkyl halides, rates of reduction;	100%
With sodium ammonium; ammonia
With aluminium amalgam

: 626-67-5
N-methylcyclohexylamine

: 542-69-8
1-iodo-butane

: 37971-78-1
1-butyl-1-methylpiperidinium iodide

Conditions

Conditions	Yield
In chloroform at 60℃; for 6h;	100%
In chloroform Heating;

: 542-69-8
1-iodo-butane

: 16199-06-7
potassium pyrrolide

: 589-33-3
N-butylpyrrole

Conditions

Conditions	Yield
In tetrahydrofuran at 20℃; for 16h;	100%

: 542-69-8
1-iodo-butane

: 127491-67-2
2,8,9-Trimethyl-2,5,8,9-tetraaza-1-phospha-bicyclo[3.3.3]undecane 1-sulfide

: 1-Butylsulfanyl-2,8,9-trimethyl-2,8,9-triaza-5-azonia-1λ5-phospha-tricyclo[3.3.3.01,5]undecane; iodide

Conditions

Conditions	Yield
In acetonitrile at 50 - 55℃; for 96h;	100%

: 542-69-8
1-iodo-butane

: C10H21N4PS2

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

Conditions

Conditions	Yield
In [D3]acetonitrile	100%

: 542-69-8
1-iodo-butane

: 176100-94-0
O,O-diethyltrimethylsilylchloromethylphosphonate α-lithie

: 118512-69-9
(1-Chloro-1-trimethylsilanyl-pentyl)-phosphonic acid diethyl ester

Conditions

Conditions	Yield
In tetrahydrofuran; hexane for 1h; Ambient temperature;	100%

: 542-69-8
1-iodo-butane

: 108-44-1
1-amino-3-methylbenzene

: 74878-72-1
N-butyl-N-(3-methyl-n-propyl)-m-toluidine

Conditions

Conditions	Yield
With sodium acetate at 130 - 140℃; for 4h;	100%

: 243-58-3
quindoline

: 542-69-8
1-iodo-butane

: 5-Butyl-10H-indolo[3,2-b]quinolin-5-ium; iodide

Conditions

Conditions	Yield
at 135℃; for 15h;	100%

: 542-69-8
1-iodo-butane

: 102463-72-9
N-benzyl-N'-dodecyl-thiourea

: C24H43N2S(1+)*I(1-)

Conditions

Conditions	Yield
In methanol	100%

: 542-69-8
1-iodo-butane

: to 2b

: C42H80N4S2(2+)*2I(1-)

Conditions

Conditions	Yield
In methanol	100%

: 542-69-8
1-iodo-butane

: 3721-95-7
Cyclobutanecarboxylic acid

: 58148-13-3
1-butylcyclobutane carboxylic acid

Conditions

Conditions	Yield
Stage #1: Cyclobutanecarboxylic acid With lithium diethylamide In tetrahydrofuran; n-heptane; ethylbenzene at 0 - 20℃; for 2h; Stage #2: 1-iodo-butane In tetrahydrofuran; n-heptane; ethylbenzene at 20℃;	100%
With lithium diisopropyl amide In tetrahydrofuran at 20℃; for 12h;
Stage #1: Cyclobutanecarboxylic acid With lithium diisopropyl amide In tetrahydrofuran; hexane at -78 - 20℃; for 1h; Stage #2: 1-iodo-butane In tetrahydrofuran at 0 - 20℃; for 12h;

: 542-69-8
1-iodo-butane

: 634198-18-8
4-(6-hydroxy-7-methoxy-4-quinazolinyl)-1-piperazinecarboxylic acid tert-butyl ester

: 634198-06-4
4-(6-butoxy-7-methoxy-4-quinazolinyl)-1-piperazinecarboxylic acid tert-butyl ester

Conditions

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

: 542-69-8
1-iodo-butane

: 10111-08-7
2-imidazolecarbaldehyde

: 169378-52-3
1-n-butyl-1H-imidazole-2-carbaldehyde

Conditions

Conditions	Yield
With potassium carbonate In N,N-dimethyl-formamide	100%
Stage #1: 2-imidazolecarbaldehyde With potassium carbonate In N,N-dimethyl-formamide Stage #2: 1-iodo-butane	82%
With potassium carbonate In DMF (N,N-dimethyl-formamide) at 50℃; for 6h;
With potassium carbonate In N,N-dimethyl-formamide at 80℃;

: 938169-94-9
C14H18N2O2

: 542-69-8
1-iodo-butane

: C18H26N2O2

Conditions

Conditions	Yield
With potassium carbonate In acetonitrile for 4h; Heating;	100%

: 542-69-8
1-iodo-butane

: (4aS,7S,7aR)-2-n-butyl-4,7-dimethyl-2,4a,5,6,7,7a-hexahydro-1H-cyclopenta[c]pyridin-1-one

Conditions

Conditions	Yield
Stage #1: (4aS,7S,7aR)-nepetalactam With potassium hydride In tetrahydrofuran at 0℃; for 0.5h; Stage #2: 1-iodo-butane In tetrahydrofuran at 0 - 20℃; for 1h;	100%

: 137-43-9
Cyclopentyl bromide

: 542-69-8
1-iodo-butane

: 205067-45-4
2-butoxy-1-methoxy-4-nitro-benzene

Conditions

Conditions	Yield
	100%

: 542-69-8
1-iodo-butane

: 2Li(1+)*GeC4(C6H5)4(2-)=Li2GeC4(C6H5)4

: 122951-51-3
1,1-dibutyl-2,3,4,5-tetraphenylgermole

Conditions

Conditions	Yield
In not given	100%

: 542-69-8
1-iodo-butane

: 1030366-99-4
2,6-bis(1H-benzo[d]imidazol-1-yl)pyridine

: bis(N-butylbenzimidazolium)-2,6-pyridine diiodide

Conditions

Conditions	Yield
at 160℃; for 30h; Inert atmosphere; Neat (no solvent); Sealed tube;	100%
at 160℃; for 30h;

: 542-69-8
1-iodo-butane

: 1092379-00-4
C10H7F7OSe

: 28622-61-9
butyl phenyl selenide

Conditions

Conditions	Yield
With 1,8-diazabicyclo[5.4.0]undec-7-ene In tetrahydrofuran at 20℃; for 0.25h;	100%

: 1072-63-5
1-vinylimidazole

: 542-69-8
1-iodo-butane

: 45965-87-5
1-vinyl-3-butyl-3H-imidazol-1-ium iodide

Conditions

Conditions	Yield
In toluene at 110℃; for 24h;	100%
for 5h; Inert atmosphere; Reflux;	96%
In tert-butyl methyl ether at 20℃; for 312h;	83%
In tetrahydrofuran at 20℃; for 24h;	31%
Reflux;

: 542-69-8
1-iodo-butane

: 296273-16-0
2-bromo-N-(4-ethylphenyl)benzamide

: 2-bromo-N-butyl-N-(4-ethylphenyl)benzamide

Conditions

Conditions	Yield
Stage #1: 2-bromo-N-(4-ethylphenyl)benzamide With sodium hydride In N,N-dimethyl-formamide; mineral oil at 0℃; for 0.5h; Inert atmosphere; Stage #2: 1-iodo-butane In N,N-dimethyl-formamide; mineral oil at 0℃;	100%
Stage #1: 2-bromo-N-(4-ethylphenyl)benzamide With sodium hydride In N,N-dimethyl-formamide Stage #2: 1-iodo-butane In N,N-dimethyl-formamide

: 542-69-8
1-iodo-butane

: 852686-98-7
2-bromo-N-(4-tert-butylphenyl)benzamide

: 2-bromo-N-butyl-N-(4-tert-butylphenyl)benzamide

Conditions

Conditions	Yield
Stage #1: 2-bromo-N-(4-tert-butylphenyl)benzamide With sodium hydride In N,N-dimethyl-formamide; mineral oil at 0℃; for 0.5h; Inert atmosphere; Stage #2: 1-iodo-butane In N,N-dimethyl-formamide; mineral oil at 0℃;	100%
Stage #1: 2-bromo-N-(4-tert-butylphenyl)benzamide With sodium hydride In N,N-dimethyl-formamide Stage #2: 1-iodo-butane In N,N-dimethyl-formamide

: 542-69-8
1-iodo-butane

: 136926-09-5
2-bromo-N-(4-methylphenyl)benzamide

: 2-bromo-N-butyl-N-p-tolylbenzamide

Conditions

Conditions	Yield
Stage #1: 2-bromo-N-(4-methylphenyl)benzamide With sodium hydride In N,N-dimethyl-formamide; mineral oil at 0℃; for 0.5h; Inert atmosphere; Stage #2: 1-iodo-butane In N,N-dimethyl-formamide; mineral oil at 0℃;	100%
Stage #1: 2-bromo-N-(4-methylphenyl)benzamide With sodium hydride In N,N-dimethyl-formamide Stage #2: 1-iodo-butane In N,N-dimethyl-formamide

: 542-69-8
1-iodo-butane

: 1228692-98-5
tert-butyl (3-perfluorooctyl)propoxycarbamate

: 1228693-15-9
C20H24F17NO3

Conditions

Conditions	Yield
With caesium carbonate In acetonitrile at 45℃; for 2h;	100%

: 542-69-8
1-iodo-butane

: 10593-29-0
sodium 1-thio-β-D-glucopyranoside

: 85618-17-3
n-butyl 1-thio-β-D-glucopyranoside

Conditions

Conditions	Yield
In methanol at 20℃; for 1h;	100%

: 542-69-8
1-iodo-butane

: 956972-12-6
1,3-bis(2,6-diiopropylphenyl)imidazol-2-ylidene borane

: 1207374-64-8
1,3-bis-(2,6-diisopropylphenyl)imidazol-2-ylidene boryl iodide

Conditions

Conditions	Yield
In benzene byproducts: C12H26; 1 equiv of borane and 1 equiv of C4H9I were heated in C6H6 at 180°C for 72 h; filtered;	100%

: 542-69-8
1-iodo-butane

: (E)-N-(benzimidazol-1-yl)-1-(4-methoxyphenyl)methanimine

: (E)-N-(3-butylbenzimidazol-3-ium-1-yl)-1-(4-methoxyphenyl)methanimine iodide

Conditions

Conditions	Yield
at 100℃; for 5h;	100%
for 5h; Reflux; Inert atmosphere;	99%

: 542-69-8
1-iodo-butane

: (E)-N-(benzimidazol-1-yl)-1-(4-bromo-2-thienyl)methanimine

: (E)-1-(4-bromo-2-thienyl)-N-(3-butylbenzimidazol-3-ium-1-yl)methanimine iodide

Conditions

Conditions	Yield
at 100℃; for 5h;	100%

: 542-69-8
1-iodo-butane

: (E)-N-(benzimidazol-1-yl)-1-(p-tolyl)methanimine

: (E)-N-(3-butylbenzimidazol-3-ium-1-yl)-1-(p-tolyl)methanimine iodide

Conditions

Conditions	Yield
at 100℃; for 5h;	100%

: 542-69-8
1-iodo-butane

: 81949-16-8
N-(benzimidazol-1-yl)-1-(4-nitrophenyl)methanimine

: 1289374-93-1
N-(3-butylbenzimidazol-3-ium-1-yl)-1-(4-nitrophenyl)methanimine iodide

Conditions

Conditions	Yield
at 100℃; for 5h;	100%

1-Iodobutane Specification

1.Introduction of 1-Iodobutane

1-Iodobutane, with its CAS register No 542-69-8, is a kind of colorless or pale orange clear liquid. It has synonyms of Butyl iodide;1-Iodobutane Butyl iodide;1-Butyliodide;Butane,1-iodo- and 1-Jodbutan [Czech]. 1-Iodobutane should be stored in shady and cool warehouse and mainly used as solvent.

2.Properties of 1-Iodobutane

(1) Freely Rotating Bonds: 2 (2) Polar Surface Area: 0 Å2 (3) Index of Refraction: 1.503 (4) Molar Refractivity: 33.54 cm3
(5) Molar Volume: 113.3 cm3 (6) Polarizability: 13.3 ×10-24cm3 (7) Surface Tension: 29.9 dyne/cm (8) Density: 1.622 g/cm3
(9) Flash Point: 33.3 °C (10) Enthalpy of Vaporization: 34.66 kJ/mol (11) Boiling Point: 130.9 °C at 760 mmHg
(12) Vapour Pressure: 11.7 mmHg at 25°C

3.Structure descriptors of 1-Iodobutane

SMILES:ICCCC

Std. InChI:InChI=1S/C4H9I/c1-2-3-4-5/h2-4H2,1H3

Std. InChIKey:KMGBZBJJOKUPIA-UHFFFAOYSA-N

4.Safety information of 1-Iodobutane

Hazard Codes: Harmful Xn
Risk Statements: 10-20-36/37/38-20/22
R10: Flammable.
R20: Harmful by inhalation.
R36/37/38: Irritating to eyes, respiratory system and skin.
R20/22: Harmful by inhalation and if swallowed.
Safety Statements: 16-36-36/37/39-26
S16: Keep away from sources of ignition.
S36: Wear suitable protective clothing.
S36/37/39: Wear suitable protective clothing, gloves and eye/face protection.
S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
RIDADR: UN 1993 3/PG 3
WGK Germany: 3
RTECS: EK4400000
F: 8
HazardClass: 3
PackingGroup: III
HS Code: 29033080

5.Toxicity date of 1-Iodobutane

1.	mouseLD50:101 mg/kg	"Toxicometric Parameters of Industrial Toxic Chemicals Under Single Exposure," Izmerov, N.F., et al., Moscow, Centre of International Projects, GKNT, 1982Vol. -, Pg. 30, 1982.
2.	ratLD50:6100mg/m3/4H	"Toxicology of Drugs and Chemicals," Deichmann, W.B., New York, Academic Press, Inc., 1969Vol. -, Pg. 756, 1969.
3.	ratLD50:692mg/kg	"Toxicometric Parameters of Industrial Toxic Chemicals Under Single Exposure," Izmerov, N.F., et al., Moscow, Centre of International Projects, GKNT, 1982Vol. -, Pg. 30, 1982.

Product Name

1-Iodobutane

Synthetic route

1-Iodobutane Specification

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