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2-Iodoxybenzoic acid

2-Iodoxybenzoic acid Structure
2-Iodoxybenzoic acid structure
CAS No.
61717-82-6
Chemical Name:
2-Iodoxybenzoic acid
Synonyms
IBX;1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione;1-HYDROXY-1,2-BENZIODOXOL-3(1H)-ONE 1-OXIDE;BX;1-hydroxy-1-oxo-3H-1$l^{5},2-benziodaoxol-3-one;39.0%(T);TRILON®TRILON®BX;Iodoxybenzoic aci;2-IodoxybenzoicAci
CBNumber:
CB3194863
Molecular Formula:
C7H5IO4
Molecular Weight:
280.02
MDL Number:
MFCD02912492
MOL File:
61717-82-6.mol
Last updated:2026-01-13 11:16:47
Product description Number Pack Size Price
2-Iodoxybenzoic acid contains stabilizer, 45wt. % (IBX) 661384 1g $55.76
2-Iodoxybenzoic acid contains stabilizer, 45wt. % (IBX) 661384 10g $193
2-Iodoxybenzoic Acid (stabilized with Benzoic Acid + Isophthalic Acid) >39.0%(T) I0791 5g $73
2-Iodoxybenzoic Acid (stabilized with Benzoic Acid + Isophthalic Acid) >39.0%(T) I0791 25g $227
2-Iodoxybenzoic acid contains stabilizer, 45wt. % (IBX) 661384 50g $758
More product size
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2-Iodoxybenzoic acid Properties

Melting point 280 °C
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
solubility DMSO (Very Slightly, Heated)
form powder to crystal
color White to Almost white
Merck 14,5048
InChI InChI=1S/C7H5IO4/c9-7(10)5-3-1-2-4-6(5)8(11)12/h1-4H,(H,9,10)
InChIKey CQMJEZQEVXQEJB-UHFFFAOYSA-N
SMILES C1(C(=O)O)C=CC=CC=1I(=O)=O
CAS DataBase Reference 61717-82-6(CAS DataBase Reference)
FDA UNII 3K0C43POH0
UNSPSC Code 12352005
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictogramsGHS hazard pictograms
GHS05,GHS07,GHS08
Signal word  Danger
Hazard statements  H314-H335-H372
Precautionary statements  P260-P270-P280-P303+P361+P353-P305+P351+P338-P314
target organs Lungs, Respiratory system
PPE Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
Hazard Codes  C,Xi,Xn
Risk Statements  22-34-44-42/43-36/37/38-20/21/22-37-35-1
Safety Statements  26-36/37/39-45-22-35
RIDADR  UN 1759 8/PG 2
WGK Germany  3
HazardClass  8
PackingGroup  Ⅱ
HS Code  29163990
Storage Class 6.1C - Combustible acute toxic Cat.3
toxic compounds or compounds which causing chronic effects
Hazard Classifications Eye Dam. 1
Skin Corr. 1
STOT RE 1 Inhalation
STOT SE 3
Limited Quantities 1.0 L (0.3 gallons) (liquid) or 1 Kg (2.2 lbs) (solid)
Excepted Quantities Max Inner Pack (30g or 30ml) and Max Outer Pack (500g or 500ml)
NFPA 704
1
2 2

2-Iodoxybenzoic acid price More Price(24)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 661384 2-Iodoxybenzoic acid contains stabilizer, 45wt. % (IBX) 61717-82-6 1g $55.76 2025-07-31 Buy
Sigma-Aldrich 661384 2-Iodoxybenzoic acid contains stabilizer, 45wt. % (IBX) 61717-82-6 10g $193 2025-07-31 Buy
TCI Chemical I0791 2-Iodoxybenzoic Acid (stabilized with Benzoic Acid + Isophthalic Acid) >39.0%(T) 61717-82-6 5g $73 2025-07-31 Buy
TCI Chemical I0791 2-Iodoxybenzoic Acid (stabilized with Benzoic Acid + Isophthalic Acid) >39.0%(T) 61717-82-6 25g $227 2025-07-31 Buy
Sigma-Aldrich 661384 2-Iodoxybenzoic acid contains stabilizer, 45wt. % (IBX) 61717-82-6 50g $758 2025-07-31 Buy
Product number Packaging Price Buy
661384 1g $55.76 Buy
661384 10g $193 Buy
I0791 5g $73 Buy
I0791 25g $227 Buy
661384 50g $758 Buy

2-Iodoxybenzoic acid Chemical Properties,Uses,Production

Chemical Properties

White to off-white powder, prills or agglomerates

Uses

2-Iodoxybenzoic Acid is used in the oxidation of alcohols in organic synthesis. It is also frequently used in the preparation of Dess-Martin periodinane.

Uses

Stabilized 2-Iodoxybenzoic Acid (SIBX)

Definition

ChEBI: A benziodoxole compound having hydroxy and oxo substituents at the 1-position and an oxo substituent at the 3-position.

Synthesis Reference(s)

The Journal of Organic Chemistry, 48, p. 4155, 1983 DOI: 10.1021/jo00170a070

reaction suitability

reagent type: oxidant

Synthesis

2-Iodobenzoic acid

88-67-5

2-Iodoxybenzoic acid

61717-82-6

General procedure for the synthesis of 2-iodobenzoic acid from 2-iodobenzoic acid: note: IBX may explode when subjected to shock or heated to over 200 °C. IBX was prepared with reference to the method described by Sputore and coworkers.In a 500 mL round bottom flask equipped with a mechanical stirrer, 2-iodobenzoic acid (12.5 g, 50.4 mmol) was added to a solution of Oxone (40.281 g, 65.5 mmol) in deionized water (163 mL). The reaction mixture was heated to 73 °C and stirred vigorously at this temperature for 3 hours. Subsequently, the reaction mixture was cooled to 0 °C and continued to stir slowly for 1.5 hours. The mixture was filtered through a porous glass funnel and the resulting white solid was washed sequentially with deionized water (730 mL) and acetone (235 mL). Finally, the product was dried under high vacuum for 2 days to afford 2-iodoylbenzoic acid as a white solid in 84% yield (11.848 g, 42.3 mmol).

References

[1] European Journal of Organic Chemistry, 2012, # 7, p. 1439 - 1447
[2] Journal of Organic Chemistry, 1983, vol. 48, # 22, p. 4155 - 4156
[3] Journal of the American Chemical Society, 1991, vol. 113, # 19, p. 7277 - 7287
[4] Journal of Organic Chemistry, 2005, vol. 70, # 17, p. 6991 - 6994
[5] Tetrahedron, 2002, vol. 58, # 23, p. 4573 - 4587

2-Iodoxybenzoic acid Preparation Products And Raw materials

Raw materials

2-Iodobenzoic acid Isophthalic acid Potassium bromate Benzoic acid Sulfuric acid
o-Iodobenzoic acid sodium salt 1-Hydroxy-2-oxa-1-ioda(III)indan-3-one 2-Iodosobenzoic acid POTASSIUM PEROXYMONOSULFATE

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Preparation Products

Dess-Martin periodinane (5-BROMOTHIOPHEN-3-YL)METHANESULFONYL CHLORIDE 2,4-Dimethyl-3-pentanol Pinacol 2-Methyl-2-butanol

2-Iodoxybenzoic acid Suppliers

Global( 366)Suppliers
Supplier Tel Email Country ProdList Advantage
Shaanxi Haibo Biotechnology Co., Ltd 		+undefined18602966907 qinhe02@xaltbio.com China 997 58
Capot Chemical Co.,Ltd. 		+86-（0）57185586718; +8613336195806 sales@capot.com China 29735 60
Shanghai Daken Advanced Materials Co.,Ltd 		+86-2158073036 info@dakenam.com China 13799 58
Henan Tianfu Chemical Co.,Ltd. 		+86-0371-55170693 +86-19937530512 info@tianfuchem.com China 21597 55
Nanjing ChemLin Chemical Industry Co., Ltd. 		025-83697070 product@chemlin.com.cn CHINA 3009 60
Fluoropharm Co., Ltd. 		+86-0571-85586753 +86-13336034509 sales@fluoropharm.com China 1445 60
career henan chemical co 		+86-0371-86658258 +8613203830695 sales@coreychem.com China 29831 58
QINGDAO HONG JIN CHEMCIAL CO.,LTD. 		+86-86-532-83657313 +86-18663969289 hjt@hong-jin.com China 226 58
Hubei xin bonus chemical co. LTD 		86-13657291602 linda@hubeijusheng.com CHINA 22963 58
CONIER CHEM AND PHARMA LIMITED 		+8618523575427 sales@conier.com China 49977 58
Supplier Advantage
Shaanxi Haibo Biotechnology Co., Ltd 		58
Capot Chemical Co.,Ltd. 		60
Shanghai Daken Advanced Materials Co.,Ltd 		58
Henan Tianfu Chemical Co.,Ltd. 		55
Nanjing ChemLin Chemical Industry Co., Ltd. 		60
Fluoropharm Co., Ltd. 		60
career henan chemical co 		58
QINGDAO HONG JIN CHEMCIAL CO.,LTD. 		58
Hubei xin bonus chemical co. LTD 		58
CONIER CHEM AND PHARMA LIMITED 		58

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View Lastest Price from 2-Iodoxybenzoic acid manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
2-Iodoxybenzoic acid pictures 2026-02-13 2-Iodoxybenzoic acid
61717-82-6
 US $0.00-0.00 / kg 1kg 98% 20MT Watson Biotechnology Co.,Ltd
2-Iodoxybenzoic acid pictures 2024-04-12 2-Iodoxybenzoic acid
61717-82-6
 US $0.00 / kg 1kg 99% 2000ton Shaanxi Haibo Biotechnology Co., Ltd
2-Iodoxybenzoic Acid pictures 2021-07-13 2-Iodoxybenzoic Acid
61717-82-6
 US $15.00-10.00 / KG 1KG 99%+ HPLC Monthly supply of 1 ton Zhuozhou Wenxi import and Export Co., Ltd
  • 2-Iodoxybenzoic Acid pictures
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    61717-82-6
  • US $15.00-10.00 / KG
  • 99%+ HPLC
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2-Iodoxybenzoic acid Spectrum

2-Iodoxybenzoic acid(61717-82-6)FT-IR

61717-82-6(2-Iodoxybenzoic acid)Related Search:

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O-IODOXYBENZOIC ACID, 97% 2-Iodotoluene Iodosobenzene 1-HYDROXY-1,3-DIOXO-1,3-DIHYDRO-1L5-BENZO[D][1,2]IODOXOLE-4-CARBOXYLIC ACID Iodoxybenzene
2-Iodoxybenzoic acid 2-IODOXYBENZOIC ACID STABILIZED MIXTURE (DESS MART STABILIZED 2-IODOXYBENZOIC ACID (SIBIX) MIXTURE

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1-hydroxy-1-oxo-3H-1$l^{5},2-benziodaoxol-3-one 2-Iodoxybenzoic Acid Stabilized (SIBX) 2-Iodoxybenzoic Acid (stabilized with Benzoic Acid + Isophthalic Acid) 1-Hydroxy-1,2-benziodoxol-3(1H)-one 1-oxide 97%, 45 wt. % IBX SIBX, 1,3-Dihydro-1,3-dioxo-1-hydroxy-1,2-benziodoxole stabilised Iodoxybenzoic aci 2-Iodoxybenzoic acid contains stabilizer, 45 wt. % (IBX) TRILON® TRILON®BX 2-IODOXYBENZOIC ACID (IBX) 1M SOLUTION IN DMSO 1-Hydroxy-1,2-benziodoxol-3(1H)-one 1-oxide (mixture of isomers) 1,2-BENZIODOXOL-3(1H)-ONE, 1-HYDROXY, 1-OXIDE 1-HYDROXY-1,2-BENZIODOXOL-3(1H)-ONE 1-OXIDE 1-HYDROXY-1,2-BENZIODOXOL-3(H)-ONE 1-OXIDE 2-IODOXYBENZOIC ACID, STABILIZED (45 WT& IbxO-IodoxybenzoicAcid 2-Iodoxybenzoic acid, stabilized 2-Iodoxybenzoic acid IBX(1-HYDROXY-1,2-BENZIODOXOL-3(1H)-ONE-1-OXIDE) SIBX, Stabilized IBX 2-Iodoxybenzoic acid ,39-50% [Stabilizer：Benzoic acid 23%，Isophtalic acid 30%] 1-Hydroxy-1,3-dioxo-3H-benz[d][1,2]iodoxol 1-Hydroxy-3H-benz[d][1,2]iodoxol-1,3-dione 2-Iodoxybenzoic acidDess Martin analogueSIBX 1-Hydroxy-1,2-benziodoxy-3-(1h)-one-1-xoide 2-Iodoxybenzoic Acid Stabilized (SIBX), 46 wt% IBX 1-Hydroxy-1,2-benziodoxol-3(1H)-one 1-oxide 97% BX IBX, 1,3-Dihydro-1,3-dioxo-1-hydroxy-1,2-benziodoxole 1-hydroxy-1,3-dioxobenziodoxole IBX 1-hydroxy-1-oxo-1$l^{5},2-benziodoxol-3-one 2-Iodoxybenzoic acid (mixture of isomers) 2-Iodoxybenzoic acid, stabilized (45 wt.% IBX) 2-Iodoxybenzoic acid(IBX) 2-IodoxybenzoicAcid(stabilizedwithBenzoicAcid+IsophthalicAcid)> 39.0%(T) 2-Iodoxybenzoic Acid,>95% 2-Iodoxybenzoic acid (Stabilised) 2-IodoxybenzoicAci 2-Iodoxybenzoic acid, contains stabilizer, 0.45wt (IBX) 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione 2-Iodoxybenzoic acid contains stabilizer 1-hydroxy-1-oxo-3H-1λ?,2-benziodaoxol-3-one Stabilised IBX [Stabilised iodoxy benzoic acid} 1-hydroxy-1-oxo-3H-1lambda5,2-benziodaoxol-3-one IBX,contains stabilizer, 45-47wt% 2-Iodoacylbenzoic acid 1-Hydroxy-1,2-benziodoxol-3(1H)-one 1-oxide, 45 wt. % IBX 1-HYDROXY-1,2-BENZIODOXOL-3(H)-ONE 1-OXIDE (45% W/W WITH STABLIZER) 61717-82-6 C7H5IO4 Hypervalent Iodine Oxidation Synthetic Reagents Fused Ring Systems pharmacetical API intermediates