2-Iodobutane

Base Information Edit

Chemical Name:2-Iodobutane
CAS No.:513-48-4
Deprecated CAS:52152-71-3
Molecular Formula:C₄H₉I
Molecular Weight:184.02
Hs Code.:29033080
European Community (EC) Number:208-163-1
NSC Number:8422
UN Number:2390
UNII:4302E40S4N
DSSTox Substance ID:DTXSID40858729
Nikkaji Number:J2.621B
Wikidata:Q27258588
Mol file:513-48-4.mol

Synonyms:2-IODOBUTANE;sec-Butyl iodide;513-48-4;2-Butyl iodide;Butane, 2-iodo-;sec-Iodobutane;2-Jodbutan;2-Jodbutan [Czech];NSC 8422;EINECS 208-163-1;UN2390;BRN 1718777;UNII-4302E40S4N;NSC-8422;4302E40S4N;2-01-00-00086 (Beilstein Handbook Reference);2-iodanylbutane;2-iodobutan;2-iodo-butane;sec.-butyl iodide;Butano, 2-yodo-;1219795-41-1;sec-C4H9I;2-IODOBUTANE-D9;SCHEMBL99121;WLN: IY2&1;(+/-)-2-IODOBUTANE;IQRUSQUYPCHEKN-UHFFFAOYSA-;DTXSID40858729;NSC8422;MFCD00001072;NA2390;Butane, 2-iodo-, (.+/-.)-;AKOS009157016;SEC-BUTYL IODIDE DL-FORM [MI];UN 2390;LS-45923;2-Iodobutane, contains copper as stabilizer;2-Iodobutane [UN2390] [Flammable liquid];B1093;FT-0612675;2-Iodobutane [UN2390] [Flammable liquid];EN300-1265839;A828546;J-802088;2-Iodobutane, >=98%, contains copper as stabilizer;Q27258588;F2190-0175

Suppliers and Price of 2-Iodobutane

Supply Marketing:Edit

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

TRC
2-Iodobutane
25g
$ 140.00

TCI Chemical
2-Iodobutane (stabilized with Copper chip) >98.0%(GC)
500g
$ 165.00

TCI Chemical
2-Iodobutane (stabilized with Copper chip) >98.0%(GC)
25g
$ 25.00

SynQuest Laboratories
2-Iodobutane 99%
100 g
$ 106.00

SynQuest Laboratories
2-Iodobutane 99%
500 g
$ 264.00

Sigma-Aldrich
2-Iodobutane ≥98%, contains copper as stabilizer
100g
$ 80.00

Sigma-Aldrich
2-Iodobutane ≥98%, contains copper as stabilizer
5g
$ 39.70

Oakwood
2-Iodobutane,containscopperasstabilizer 98%
25g
$ 25.00

Medical Isotopes, Inc.
2-Iodobutane
100 g
$ 675.00

Matrix Scientific
2-Iodobutane 95%+
5g
$ 1216.00

Total 20 raw suppliers

Chemical Property of 2-Iodobutane Edit

Chemical Property:

Appearance/Colour:liquid
Vapor Pressure:18.6mmHg at 25°C
Melting Point:-104 °C
Refractive Index:n20/D 1.499(lit.)
Boiling Point:119-120 °C(lit.)
Flash Point:21 ºC
PSA：0.00000
Density:1.598
LogP:2.21990
Storage Temp.:Flammables area
Sensitive.:Light Sensitive
Solubility.:alcohol: soluble(lit.)
Water Solubility.:Insoluble in water. Soluble in alcohol and diethyl ether.
XLogP3:2.8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:0
Rotatable Bond Count:1
Exact Mass:183.97490
Heavy Atom Count:5
Complexity:19.6
Transport DOT Label:Flammable Liquid

Purity/Quality:

98%min ^*data from raw suppliers

2-Iodobutane ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:Xi,F
Statements: 10-36/37/38
Safety Statements: 26-36

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

Chemical Classes:Other Classes -> Halogenated Aliphatics, Saturated
Canonical SMILES:CCC(C)I
Uses It is used as a solvent organic synthesis and as pharmaceutical intermediate.

Technology Process of 2-Iodobutane

There total 35 articles about 2-Iodobutane which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 98.0%

: 78-92-2,15892-23-6
iso-butanol

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

Guidance literature:: With potassium iodide; In acetonitrile; at 20 ℃; for 0.583333h;

Reference yield: 35.0%

: 106-97-8,9003-29-6,9021-92-5
n-butane

: 542-69-8
1-iodo-butane

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

Guidance literature:: With tert-butylhypochlorite; mercury(II) iodide; In 1,1,2-Trichloro-1,2,2-trifluoroethane; at 47 ℃; for 8h; Yield given; Irradiation;
DOI:10.1021/ja00330a038