MilliporeSigma
All Photos(2)

148938

Sigma-Aldrich

2-Iodopropane

contains copper as stabilizer, 99%

Sign Into View Organizational & Contract Pricing

Select a Size

Synonym(s):
Isopropyl iodide
Linear Formula:
(CH3)2CHI
CAS Number:
Molecular Weight:
169.99
Beilstein:
1098244
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

99%

form

liquid

contains

copper as stabilizer

refractive index

n20/D 1.498 (lit.)

bp

88-90 °C (lit.)

mp

−90 °C (lit.)

density

1.703 g/mL at 25 °C (lit.)

SMILES string

CC(C)I

InChI

1S/C3H7I/c1-3(2)4/h3H,1-2H3

InChI key

FMKOJHQHASLBPH-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

Compare Similar Items

View Full Comparison

Show Differences

1 of 4

This Item
238414614734342017
2-Iodopropane contains copper as stabilizer, 99%

Sigma-Aldrich

148938

2-Iodopropane

1,3-Diiodopropane 99%, contains copper as stabilizer

Sigma-Aldrich

238414

1,3-Diiodopropane

1-Iodopropane-d7 ≥98 atom % D, ≥99% (CP), contains copper as stabilizer

Sigma-Aldrich

614734

1-Iodopropane-d7

form

liquid

form

liquid

form

-

form

liquid

refractive index

n20/D 1.498 (lit.)

refractive index

n20/D 1.642 (lit.)

refractive index

-

refractive index

n20/D 1.329 (lit.)

bp

88-90 °C (lit.)

bp

111-113 °C/31 mmHg (lit.)

bp

101-102 °C (lit.)

bp

40 °C (lit.)

mp

−90 °C (lit.)

mp

-

mp

-101 °C (lit.)

mp

-

density

1.703 g/mL at 25 °C (lit.)

density

2.576 g/mL at 25 °C (lit.)

density

1.820 g/mL at 25 °C

density

2.08 g/mL at 25 °C (lit.)

General description

2-Iodopropane is an organ iodine compound. It is commonly used as a homolytic and heterolytic alkylating agent and in the preparation of the α-isopropoxymethylene blocking group. Additionally, it acts as an intermediator in the conversion of thiocarbonate to alkene.

Application

2-Iodopropane (Isopropyl iodide) was used to prepare butyric and isobutyric acid.

2-Iodopropane is used as an alkylating agent in the conversion of phenols, alcohols, oximes, carboxylic acids, and heteroatomic compounds (indoles, pyridines, purines, tetrazoles, pyrazoles, and amines) to give corresponding products.

Pictograms

FlameExclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

107.6 °F - closed cup

Flash Point(C)

42 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Documents related to the products that you have purchased in the past have been gathered in the Document Library for your convenience.

Visit the Document Library

Difficulty Finding Your Product Or Lot/Batch Number?

Product numbers are combined with Pack Sizes/Quantity when displayed on the website (example: T1503-25G). Please make sure you enter ONLY the product number in the Product Number field (example: T1503).

Example:

T1503
Product Number
-
25G
Pack Size/Quantity

Additional examples:

705578-5MG-PW

PL860-CGA/SHF-1EA

MMYOMAG-74K-13

1000309185

enter as 1.000309185)

Having trouble? Feel free to contact Technical Service for assistance.

Lot and Batch Numbers can be found on a product's label following the words 'Lot' or 'Batch'.

Aldrich Products

  • For a lot number such as TO09019TO, enter it as 09019TO (without the first two letters 'TO').

  • For a lot number with a filling-code such as 05427ES-021, enter it as 05427ES (without the filling-code '-021').

  • For a lot number with a filling-code such as STBB0728K9, enter it as STBB0728 without the filling-code 'K9'.

Not Finding What You Are Looking For?

In some cases, a COA may not be available online. If your search was unable to find the COA you can request one.

Request COA

Customers Also Viewed

Slide 1 of 7

1 of 7

Iodomethane contains copper as stabilizer, ReagentPlus®, 99.5%

Sigma-Aldrich

289566

Iodomethane

Iodomethane solution 2.0 M in tert-butyl methyl ether, contains copper as stabilizer

Sigma-Aldrich

456756

Iodomethane solution

o-Xylene puriss. p.a., ≥99.0% (GC)

Sigma-Aldrich

95662

o-Xylene

2-Iodopropane-1-13C ≥99 atom % 13C, ≥99% (CP), contains copper as stabilizer

Sigma-Aldrich

603724

2-Iodopropane-1-13C

Adipic acid 99%

Sigma-Aldrich

A26357

Adipic acid

Hydriodic acid 57 wt. % in H2O, distilled, stabilized, 99.95%

Sigma-Aldrich

210021

Hydriodic acid

2-Iodopropane
Wilson PD and Hilmey DG
Encyclopedia of Reagents for Organic Synthesis, Second Edition (2001)
Timur Coskun et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 19(21), 6840-6844 (2013-03-29)
Glycerol is converted to a mixture of butyric and isobutyric acid by rhodium- or iridium-catalysed carbonylation using HI as the co-catalyst. The initial reaction of glycerol with HI results in several intermediates that lead to isopropyl iodide, which upon carbonylation
Joe Rashan et al.
Journal of AOAC International, 86(4), 694-702 (2003-09-26)
An alternative liquid chromatographic (LC) method was developed and validated for the simultaneous determination of methoxyl and 2-hydroxypropoxyl substituents in hypromellose and hypromellose acetate succinate. The method uses the hydriodic acid cleavage reaction, catalyzed by adipic acid, of the substituted
John J Orlando et al.
The journal of physical chemistry. A, 109(30), 6659-6675 (2006-07-13)
The reaction of Cl atoms with iodoethane has been studied via a combination of laser flash photolysis/resonance fluorescence (LFP-RF), environmental chamber/Fourier transform (FT)IR, and quantum chemical techniques. Above 330 K, the flash photolysis data indicate that the reaction proceeds predominantly
Development and validation of analytical procedure--control of residual 2-iodopropane in latanoprost.
Aleksandra Groman et al.
Acta poloniae pharmaceutica, 67(6), 673-676 (2011-01-15)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service