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2-Iodophenol - 98%, high purity , CAS No.533-58-4

5 Citations

COA

Grade & Purity:

≥98%

Cas Number: 533-58-4
Molecular Weight: 220.01
EC Number: 208-569-9
MDL number: MFCD00013963
PubChem CID: 10784
PubChem SID: 504752001

In stock

Item Number

I107036

Grouped product items
SKU	Size	Availability	Price
I107036-5g	5g	3	$9.90
I107036-10g	10g	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$15.90
I107036-25g	25g	3	$25.90
I107036-100g	100g	1	$82.90
I107036-500g	500g	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$329.90

View related series

Non heterocyclic block (8163) phenol (506)

Basic Description

Synonyms	O-IODOPHENOL [MI] \| 2-iodanylphenol \| DTXSID5052175 \| Phenol, o-iodo- \| 2-IODOPHENOL \| 2-iodo-phenol \| 6X8 \| EN300-39648 \| 4-06-00-01070 (Beilstein Handbook Reference) \| WLN: QR BI \| 2-Iodophenol (2IP) \| J-200045 \| AKOS009156984 \| EINECS 208-569-9 \| STL28
Specifications & Purity	≥98%
Storage Temp	Store at 2-8°C,Protected from light,Argon charged
Shipped In	Wet ice This product requires cold chain shipping. Ground and other economy services are not available.
Product Description	Rapid palladium-catalyzed carbonylative cyclization reactions of 2-iodophenol with various alkyne under microwave irradiation using Mo(CO)6 as the CO source has been investigated. It was used in the synthesis of: aryl 2-benzofuranyl and aryl 2-indolyl carbinols of high enantiomeric purity; 3,3-disubstituted-2,3-dihydrobenzofuran.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Benzenoids
  - Class Phenols
    - Subclass Halophenols
      - Level5 Iodophenols
        Level6 O-iodophenols

Kingdom	Organic compounds
Superclass	Benzenoids
Class	Phenols
Subclass	Halophenols
Intermediate Tree Nodes	Iodophenols
Direct Parent	O-iodophenols
Alternative Parents	Iodobenzenes 1-hydroxy-4-unsubstituted benzenoids 1-hydroxy-2-unsubstituted benzenoids Aryl iodides Organooxygen compounds Organoiodides Hydrocarbon derivatives
Molecular Framework	Aromatic homomonocyclic compounds
Substituents	2-iodophenol - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Iodobenzene - Halobenzene - Monocyclic benzene moiety - Aryl iodide - Aryl halide - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Organoiodide - Organohalogen compound - Aromatic homomonocyclic compound
Description	This compound belongs to the class of organic compounds known as o-iodophenols. These are iodophenols carrying a iodine at the C2 position of the benzene ring.
External Descriptors	an iodoaromatic compound
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Mechanisms of Action

Mechanism of Action	Action Type	target ID	Target Name	Target Type	Target Organism	Binding Site Name	References

Names and Identifiers

Pubchem Sid	504752001
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/504752001
IUPAC Name	2-iodophenol
INCHI	InChI=1S/C6H5IO/c7-5-3-1-2-4-6(5)8/h1-4,8H
InChIKey	KQDJTBPASNJQFQ-UHFFFAOYSA-N
Smiles	C1=CC=C(C(=C1)O)I
Isomeric SMILES	C1=CC=C(C(=C1)O)I
WGK Germany	3
RTECS	SL5500000
UN Number	2811
Molecular Weight	220.01
Reaxy-Rn	1855300
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1855300&ln=

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

18 results found

Lot Number	Certificate Type	Date	Item
C2527559	Certificate of Analysis	Mar 14, 2025	I107036
C2527557	Certificate of Analysis	Mar 14, 2025	I107036
C2527558	Certificate of Analysis	Mar 14, 2025	I107036
C2527554	Certificate of Analysis	Mar 14, 2025	I107036
C2527555	Certificate of Analysis	Mar 14, 2025	I107036
C2527556	Certificate of Analysis	Mar 14, 2025	I107036
L2205579	Certificate of Analysis	Sep 13, 2024	I107036
L2205029	Certificate of Analysis	Sep 13, 2024	I107036
L2205046	Certificate of Analysis	Sep 13, 2024	I107036
I2425431	Certificate of Analysis	Jul 01, 2024	I107036
I2425428	Certificate of Analysis	Jul 01, 2024	I107036
I2425429	Certificate of Analysis	Jul 01, 2024	I107036
D2117171	Certificate of Analysis	Jan 15, 2023	I107036
D2117173	Certificate of Analysis	Jan 15, 2023	I107036
D2117172	Certificate of Analysis	Jan 15, 2023	I107036
L2205021	Certificate of Analysis	Sep 16, 2022	I107036
H1823118	Certificate of Analysis	Apr 26, 2022	I107036
C2016170	Certificate of Analysis	Jan 19, 2022	I107036

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Chemical and Physical Properties

Solubility	Solubility in water: slightly soluble Solubility in other solvents: soluble in ethanol and ether
Sensitivity	Light & air Sensitive
Flash Point(°F)	235.4 °F
Flash Point(°C)	113 °C
Boil Point(°C)	186-187°C
Melt Point(°C)	37-43°C
Molecular Weight	220.010 g/mol
XLogP3	2.600
Hydrogen Bond Donor Count	1
Hydrogen Bond Acceptor Count	1
Rotatable Bond Count	0
Exact Mass	219.939 Da
Monoisotopic Mass	219.939 Da
Topological Polar Surface Area	20.200 Å²
Heavy Atom Count	8
Formal Charge	0
Complexity	74.900
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

Citations of This Product

How to Cite Aladdin Scientific Products?

1. Chao Fang,Stuart W Krasner,Wenhai Chu,Shunke Ding,Tiantao Zhao,Naiyun Gao. (2018-08-20) Formation and speciation of chlorinated, brominated, and iodinated haloacetamides in chloraminated iodide-containing waters.. Water research, 145 (103-112).
2. Pengjia Sun, Jian Xiong, Ping Sun, Yingsen Fang, Hongxia Liu, Hui Liu, Bitao Xiong, Hui Wang, Xing'ao Li. (2024) Additional O doping significantly improved the catalytic performance of Mn/O co-doped g-C3N4 for activating periodate and degrading organic pollutants. SEPARATION AND PURIFICATION TECHNOLOGY, 331 (125593).
3. Pengjia Sun, Ping Sun, Yingsen Fang, Hui Liu, Bitao Xiong, Hui Wang, Xingao Li. (2023) Enhanced degradation of bisphenol S in water using a combination process of electrochemical oxidation with periodate activation. Journal of Water Process Engineering, 55 (104203).
4. Li Zhijun, Zhang Mingyang, Zhang Lili, Dong Xiuli, Leng Leipeng, Horton J. Hugh, Wang Jun. (2022) Engineering the atomic interface of porous ceria nanorod with single palladium atoms for hydrodehalogenation reaction. Nano Research, 15 (2): (1338-1346).
5. Jing Liu, Jing Wang, Jie Zhang, Yang Mu. (2019) Iodo-trihalomethanes formation during chlorination and chloramination of iodide-containing waters in the presence of Cu2+. SCIENCE OF THE TOTAL ENVIRONMENT, 671 (101).

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