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138584

Sigma-Aldrich

3-Iodobenzoic acid

98%

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About This Item

Linear Formula:
IC6H4CO2H
CAS Number:
618-51-9
Molecular Weight:
248.02
Beilstein:
971088
EC Number:
210-555-2
MDL number:
MFCD00002496
UNSPSC Code:
12352100
PubChem Substance ID:
24848360
NACRES:
NA.22

Assay

98%

mp

185-187 °C (lit.)

functional group

carboxylic acid

SMILES string

OC(=O)c1cccc(I)c1

InChI

1S/C7H5IO2/c8-6-3-1-2-5(4-6)7(9)10/h1-4H,(H,9,10)

InChI key

KVBWBCRPWVKFQT-UHFFFAOYSA-N

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General description

3-Iodobenzoic acid is added as UV absorbing background electrolyte in separation of uncharged cyclodextrins and their derivatives by capillary electrophoresis.

Application

3-Iodobenzoic acid was used in solid phase synthesis of γ-turn mimetic library.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

ISHL Indicated Name

Substances Subject to be Indicated Names

ISHL Notified Names

Substances Subject to be Notified Names

JAN Code

138584-VAR:
138584-BULK:
138584-10G:4548173992631
138584-50G:4548173992648

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Certificates of Analysis (COA)

Lot/Batch Number
BCCD8176
BCCB1292
BCBW8707
BCBV8166
00323AJV

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A γ-Turn Mimetic Library: Development and Production.
Kocis P, et al.
High-Throughput Synthesis: Principles and Practices, 65-65 (2010)
M Pumera et al.
Fresenius' journal of analytical chemistry, 369(7-8), 666-669 (2001-05-24)
A fast and simple capillary electrophoretic method suitable for the determination of native alpha-, beta-, gamma-cyclodextrins, their randomly substituted tert-butyl derivatives (average degree of substitution 3.8-4.4), heptakis (2,6-di-O-methyl)- and heptakis (2,3,6-tri-O-methyl)-beta-cyclodextrin was developed. Naphthyl-2-sulfonic acid (2-NSA), 3-iodobenzoic acid (3-IBA) and
H Brasch
Archives internationales de pharmacodynamie et de therapie, 262(2), 242-249 (1983-04-01)
In guinea-pig Langendorff hearts, Na-salicylate (1.9, 3.8 and 7.6 mmol/l) concentration-dependently reduced the contractile force (--9.1, --51.0 and --75.1%, respectively) and the coronary resistance. The influence of the uncoupling agent 2.4-dinitrophenol (0.02 mmol/l) was comparable to that of the largest
Pablo Wessig et al.
Molecules (Basel, Switzerland), 18(1), 1314-1324 (2013-01-23)
Various 1,6- and 1,8-naphthalenophanes were synthesized by using the Photo-Dehydro-Diels-Alder (PDDA) reaction of bis-ynones. These compounds are easily accessible from ω-(3-iodophenyl)carboxylic acids in three steps. The obtained naphthalenophanes are axially chiral and the activation barrier for the atropisomerization could be
G Vaidyanathan et al.
Bioconjugate chemistry, 1(6), 387-393 (1990-11-01)
We have previously shown that use of N-succinimidyl 3-iodobenzoate (SIB) for radioiodination of monoclonal antibodies (MAbs) decreases the loss of radioiodine in vivo compared to MAbs labeled by using conventional methods. Herein, the synthesis of N-succinimidyl 2,4-dimethoxy-3-(trialkylstannyl)benzoates (alkyl = Me

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