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Iodobenzene

CAS No.
591-50-4
Chemical Name:
Iodobenzene
Synonyms
Phenyl iodide;iodo-benzen;1-Iodobenzene;4-Iodobenzene;Iodbenzol;iodinebenzol;Phenyliodide;benzeneiodide;Benzene,iodo-;Benzene iodide
CBNumber:
CB0700740
Molecular Formula:
C6H5I
Molecular Weight:
204.01
MDL Number:
MFCD00001029
MOL File:
591-50-4.mol
MSDS File:
SDS
Last updated:2026-08-25 20:17:46

Iodobenzene Properties

Melting point -29 °C (lit.)
Boiling point 188 °C (lit.)
Density 1.823 g/mL at 25 °C (lit.)
vapor pressure 1.41 hPa ( 25 °C)
refractive index n20/D 1.62(lit.)
Flash point 74 °C
storage temp. Store below +30°C.
solubility 0.34g/l (experimental)
form Liquid
color Clear yellow
Specific Gravity 1.823
Water Solubility insoluble
Thermal Conductivity 0.099 W/(m·K) at 25 ℃
Specific Heat Capacity Cp(liquid): 0.78 J/(g·K), at 25℃
Sensitive Light Sensitive
Merck 14,5029
BRN 1446140
Henry's Law Constant 7.7×10-3 mol/(m3Pa) at 25℃, Mackay and Shiu (1981)
Dielectric constant 4.6(20℃)
InChI 1S/C6H5I/c7-6-4-2-1-3-5-6/h1-5H
InChIKey SNHMUERNLJLMHN-UHFFFAOYSA-N
SMILES Ic1ccccc1
Surface tension 39.7mN/m at 20°C
CAS DataBase Reference 591-50-4(CAS DataBase Reference)
FDA UNII 9HK5L7YBBR
NIST Chemistry Reference Benzene, iodo-(591-50-4)
EPA Substance Registry System Benzene, iodo- (591-50-4)
UNSPSC Code 12352101
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H302
Precautionary statements  P264-P270-P301+P312-P501
PPE Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Hazard Codes  Xn,Xi
Risk Statements  22-36-20/22
Safety Statements  26-36-23
RIDADR  NA 1993 / PGIII
WGK Germany  3
RTECS  DA3390000
F  8
Hazard Note  Irritant
TSCA  TSCA listed
HS Code  29036990
Storage Class 10 - Combustible liquids
Hazard Classifications Acute Tox. 4 Oral
Hazardous Substances Data 591-50-4(Hazardous Substances Data)
REACH Registrations Active
NFPA 704
1
2 0

Iodobenzene price More Price(66)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich I7632 Iodobenzene 98% 591-50-4 5G $40.3 2026-04-30 Buy
Sigma-Aldrich I7632 Iodobenzene 98% 591-50-4 100g $87.6 2026-04-30 Buy
Sigma-Aldrich I7632 Iodobenzene 98% 591-50-4 500g $279 2026-04-30 Buy
TCI Chemical I0050 Iodobenzene 591-50-4 25G $30 2026-04-30 Buy
TCI Chemical I0050 Iodobenzene 591-50-4 100G $76 2026-04-30 Buy
Product number Packaging Price Buy
I7632 5G $40.3 Buy
I7632 100g $87.6 Buy
I7632 500g $279 Buy
I0050 25G $30 Buy
I0050 100G $76 Buy

Iodobenzene Chemical Properties, Uses, Production

Introduction

Iodobenzene is one Iodine substitution of benzene and its molecular formula is C6H5I. It Is a colorless liquid with special odor, insoluble in water, soluble in trichloromethane, ether and ethanol. It is Photosensitive and gradually turns yellow in case of light. Because the bond energy of C-I is lower than that of C-Cl and C-Br, its reactivity is much stronger. It can react with magnesium to generate grignard reagent Phenylmagnesium Iodide (PhMgI), which can be used as equivalent of phenyl anion in organic synthesis. Iodobenzene can be used as the raw material in Sonogashira coupling reaction, Heck reaction and Other metals catalyzed coupling reaction.

Chemical Properties

Colorless liquid, melting point-31.27℃, boiling point 188.3℃, 63-64℃(1.07kPa), Flash point 74 ℃,density 1.8308(20/4℃), refractive index1.6200(18.5℃)

Usage

A general reagent for organic synthesis and used as a standard liquid refractive index

Preparation

Iodobenzene is obtained through the diazotization and replacement reaction of Aniline.
Hydrochloric acid( 30%) and aniline were added to Water, stirred and cooled to 2 ℃. Then,  sodium nitrite solution was added dropwise to the above solution and the temperature was controlled to be no more than 12℃. When the last part of sodium nitrite solution was added, potassium iodide starch paper was used to determine the blue reaction endpoint.
Then, diazotization liquid was obtained.  Potassium iodide solution was added to the diazotization solution in several batches until no nitrogen was released. After cooling, the upper aqueous solution was separated from the above system. Sodium hydroxide solution (10%) was added until the pH value was 14. A distillation process was carried out and aqueous layer was separated from the distillate. The atmospheric fractionation process was arried out after drying and the fraction at184-188 ℃ was collected, which is iodobenzene with a yield of 77%.

Chemical Properties

CLEAR YELLOW LIQUID

Uses

suzuki reaction

Uses

Iodobenzene is used to prepare biphenyl and stilbene. It reacts with magnesium to form the Grignard reagent, a phenylmagnesium iodide used in organic synthesis. It finds application as a solid chlorine source by reacting with chlorine to form a complex, iodobenzene dichloride. It serves as a substrate in Sonogashira reaction which is used to form a carbon-carbon bond between a terminal alkyne and an aryl halide.

Synthesis Reference(s)

Tetrahedron Letters, 33, p. 3167, 1992 DOI: 10.1016/S0040-4039(00)79842-X
The Journal of Organic Chemistry, 53, p. 3548, 1988 DOI: 10.1021/jo00250a024

Purification Methods

Wash it with dilute aqueous Na2S2O3, then water. Dry it with CaCl2 or CaSO4, decolourise with charcoal and distil it under reduced pressure then store it with mercury or silver powder to stabilise it. [Beilstein 5 IV 688.]

108-95-2
591-50-4
Synthesis of Iodobenzene from Phenol
Global Suppliers ( 604)
Supplier Tel Email Country ProdList Advantage
Manac (SHANGHAI) TRADING CO., LTD 021-32503616 sales@manac-inc.com.cn China 161 60
Inner Mongolia Yida Chemical Technology Co., Ltd. 18967392038 67247734@qq.com China 75 58
Nantong Enwang New Materials Co.,Ltd 18912257866 739904460@qq.com China 59 58
Nantong Haigine Pharma Technology Co., Ltd 0513-86266699-8010 19040080082 sales@haigine.com China 71 58
Bisheng Chemical (Shanghai) Co., Ltd. 19852830193 19852830193 1715763880@qq.com China 4510 58
Nanbu County Chengxin Technology Co., Ltd. 0838-5675166 15883665058 nbcxkj@126.com China 956 55
J & K SCIENTIFIC LTD. 18210857532 18210857532 jkinfo@jkchemical.com China 96815 76
Sichuan Ruibo Technology Co., Ltd +86-817-5586080 China 41 69
Meryer (Shanghai) Chemical Technology Co., Ltd. 4006356688 18621169109 market03@meryer.com China 40202 62
future industrial shanghai co., ltd 400-0066400 13621662912 sales@jonln.com China 1989 65

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View Latest Price from Iodobenzene manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Iodobenzene pictures 2026-10-14 Iodobenzene
591-50-4
$12.00 1kg 99% 100mt Jinan Finer Chemical Co., Ltd
Iodobenzene pictures 2026-09-02 Iodobenzene
591-50-4
$1.00-100.00 1KG 99% Henan Fengda Chemical Co., Ltd
 Iodobenzene pictures 2026-05-28 Iodobenzene
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$5.60 1KG 99% 5000kg Hebei Chuanghai Biotechnology Co,.LTD
  • Iodobenzene pictures
  • Iodobenzene
    591-50-4
  • $12.00
  • 99%
  • Jinan Finer Chemical Co., Ltd
  • Iodobenzene pictures
  • Iodobenzene
    591-50-4
  • $1.00-100.00
  • 99%
  • Henan Fengda Chemical Co., Ltd
  •  Iodobenzene pictures
  • Iodobenzene
    591-50-4
  • $5.60
  • 99%
  • Hebei Chuanghai Biotechnology Co,.LTD
iodo-benzen Benzene,iodo- benzeneiodide iodinebenzol Iodobenzene, 97.5% IODOBENZENE AKOS BBS-00004395 3-Iodobenzene mono iodobenzene Iodobenzene, 98% 100ML IODOBENZENE, STAB. Iodobenzene98% lodobenzene Iodobenzene 97+% Vortioxetine Impurity 51 Iodobenzene> IODOBENZENE FOR SYNTHESIS 100 ML IODOBENZENE FOR SYNTHESIS 250 ML Iodobenzene ISO 9001:2015 REACH Iodobenzene iodo-benzen IODOBENZENE For Synthesis Iodobenzene 98% For Synthesis Vortioxetine Impurity 83 Iodobenzene, 99.5% 1-Iodobenzene 4-Iodobenzene Benzene iodide Iodbenzol Phenyl iodide Phenyliodide Iodobenzene,591-50-4,OLED Intermediates,organic synthetic intermediate 591-50-4 591-50-1 591504 IC6H5 C6H5l HALOGEN Building Blocks Aryl Halogenated Hydrocarbons Organic Building Blocks C6 alkyl Iodine Aryl Halogenated Hydrocarbons API intermediates Iodine Compounds Pharmaceutical Intermediate Pharmaceutical Intermediates Aromatic Halides (substituted) Organics bc0001 591-50-4 C6