Iodoacetamide - Moligand™, Ultra pure, ≥99%(NMR) , CAS No.144-48-9

Name: Iodoacetamide - Moligand™, Ultra pure, ≥99%(NMR) , CAS No.144-48-9
Brand: Aladdin Scientific
SKU: I131590
Availability: InStock

CAS: 144-48-9 Cat. No.: I131590 Formula: C₂H₄INO Molecular Weight: 184.96 Beilstein Registry Number: 1739080 EC Number: 205-630-1

112 Citations COA

Skip to the end of the images gallery

Iodoacetamide - Moligand™, Ultra pure, ≥99%(NMR) CAS No(144-48-9) by Aladdin Scientific

Skip to the beginning of the images gallery

AVAILABLE TO ORDER

GRADE & PURITY Moligand™ ? Ultra pure ? ≥99%(NMR)

Synonyms

Storage

Store at 2-8°C

Shipped In

Wet ice

Overview Specifications Names and Identifiers Documentation Advanced Data Taxonomic Classification 3D Structure Associated Targets(Human) Associated Targets(non-human) Mechanisms of Action Certificates (CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Documents & Articles Citations of This Product Solution Calculators Reviews

🧪

Why this grade

Moligand™, Ultra pure, ≥99%(NMR) Moligand™,Ultra pure for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at 2-8°C Ships Wet ice Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 112 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

Alkylating reagent for cysteine residues in peptide sequencing.

Specifications

Synonyms

Specifications & Purity

Moligand™, Ultra pure, ≥99%(NMR)

Biochemical and Physiological Mechanisms

Iodoacetamide acts as an alkylating reagent for cysteine residues in peptide sequencing. It is an irreversible inhibitor of enzymes with cysteine at the active site. It reacts much more slowly with histidine residues, but that activity is responsible for

Storage

Store at 2-8°C

Shipped In

Wet ice

This product requires cold chain shipping. Ground and other economy services are not available.

Grade

Moligand™, Ultra pure

Note

Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.

Purity

≥99%(NMR)

Names and Identifiers

Pubchem Sid

504750705

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/504750705

Canonical Smiles

C(C(=O)N)I

IUPAC Name

2-iodoacetamide

InChIKey

PGLTVOMIXTUURA-UHFFFAOYSA-N

INCHI

1S/C2H4INO/c3-1-2(4)5/h1H2,(H2,4,5)

Isomeric SMILES

C(C(=O)N)I

WGK Germany

RTECS

AC4200000

UN Number

2811

Packing Group

III

Molecular Weight

184.96

Beilstein

1739080

Reaxy-Rn

1739080

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1739080&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

<<<<<<< HEAD Download SDS → ======= Download SDS → >>>>>>> release248-p3

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organic acids and derivatives
  - Class Carboxylic acids and derivatives
    - Subclass Carboxylic acid derivatives
      - Level5 Carboxylic acid amides
        Level6 Primary carboxylic acid amides

Kingdom	Organic compounds
Superclass	Organic acids and derivatives
Class	Carboxylic acids and derivatives
Subclass	Carboxylic acid derivatives
Intermediate Tree Nodes	Carboxylic acid amides
Direct Parent	Primary carboxylic acid amides
Alternative Parents	Organopnictogen compounds Organonitrogen compounds Organoiodides Organic oxides Hydrocarbon derivatives Carbonyl compounds Alkyl iodides
Molecular Framework	Aliphatic acyclic compounds
Substituents	Primary carboxylic acid amide - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Organoiodide - Organohalogen compound - Carbonyl group - Alkyl iodide - Alkyl halide - Aliphatic acyclic compound
Description	This compound belongs to the class of organic compounds known as primary carboxylic acid amides. These are compounds comprising primary carboxylic acid amide functional group, with the general structure RC(=O)NH2.
External Descriptors	an iodide
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

3D Structure

Associated Targets(Human)

CYP3A4 Tclin Cytochrome P450 3A4 (1 Activities)

Discover Target: CYP3A4

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

TRPA1 Tclin Transient receptor potential cation channel subfamily A member 1 (1 Activities)

Discover Target: TRPA1

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

TYMS Tclin Thymidylate synthase (1651 Activities)

Discover Target: TYMS

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CHRM1 Tclin Muscarinic acetylcholine receptor M1 (12690 Activities)

Discover Target: CHRM1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

VDR Tclin Vitamin D receptor (26531 Activities)

Discover Target: VDR

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

AK2 Tbio Adenylate kinase 2 (264 Activities)

Discover Target: AK2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

POLB Tchem DNA polymerase beta (23632 Activities)

Discover Target: POLB

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

GLA Tclin Alpha-galactosidase A (5444 Activities)

Discover Target: GLA

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ARSA Tbio Cerebroside-sulfatase (655 Activities)

Discover Target: ARSA

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ALOX15B Tchem Arachidonate 15-lipoxygenase, type II (7244 Activities)

Discover Target: ALOX15B

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)

Discover Target: ALDH1A1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CYP2D6 Tclin Cytochrome P450 2D6 (33882 Activities)

Discover Target: CYP2D6

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ALOX15 Tchem Arachidonate 15-lipoxygenase (7108 Activities)

Discover Target: ALOX15

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CYP1A2 Tchem Cytochrome P450 1A2 (26471 Activities)

Discover Target: CYP1A2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CYP2C9 Tchem Cytochrome P450 2C9 (32119 Activities)

Discover Target: CYP2C9

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CYP2C19 Tchem Cytochrome P450 2C19 (29246 Activities)

Discover Target: CYP2C19

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)

Discover Target: CYP3A4

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

TP53 Tchem Cellular tumor antigen p53 (48468 Activities)

Discover Target: TP53

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

F13A1 Tchem Coagulation factor XIII (223 Activities)

Discover Target: F13A1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

HSD17B10 Tchem Endoplasmic reticulum-associated amyloid beta-peptide-binding protein (20669 Activities)

Discover Target: HSD17B10

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

EHMT2 Tchem Histone-lysine N-methyltransferase, H3 lysine-9 specific 3 (93046 Activities)

Discover Target: EHMT2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)

Discover Target: TDP1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

KDM4E Tchem Lysine-specific demethylase 4D-like (40243 Activities)

Discover Target: KDM4E

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

USP2 Tbio Ubiquitin carboxyl-terminal hydrolase 2 (8818 Activities)

Discover Target: USP2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

LMNA Tbio Prelamin-A/C (36751 Activities)

Discover Target: LMNA

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

RECQL Tbio ATP-dependent DNA helicase Q1 (5575 Activities)

Discover Target: RECQL

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

BLM Tchem Bloom syndrome protein (4248 Activities)

Discover Target: BLM

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

HPGD Tchem 15-hydroxyprostaglandin dehydrogenase [NAD+] (24926 Activities)

Discover Target: HPGD

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

THPO Tbio Thrombopoietin (834 Activities)

Discover Target: THPO

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

GMNN Tbio Geminin (128009 Activities)

Discover Target: GMNN

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

PMP22 Tbio Peripheral myelin protein 22 (699 Activities)

Discover Target: PMP22

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CBX1 Tbio Chromobox protein homolog 1 (92434 Activities)

Discover Target: CBX1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

MPHOSPH8 Tbio M-phase phosphoprotein 8 (656 Activities)

Discover Target: MPHOSPH8

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ATG4B Tchem Cysteine protease ATG4B (985 Activities)

Discover Target: ATG4B

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

RGS4 Tchem Regulator of G-protein signaling 4 (13867 Activities)

Discover Target: RGS4

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ADH1A Tclin Alcohol dehydrogenase (35 Activities)

Discover Target: ADH1A

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Associated Targets(non-human)

Saccharomyces cerevisiae (19171 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Rattus norvegicus (775804 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

GCN5 Histone acetyltransferase GCN5 (89 Activities)

Discover Target: GCN5

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Trpa1 Transient receptor potential cation channel subfamily A member 1 (1003 Activities)

Discover Target: Trpa1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

pfk 6-phospho-1-fructokinase (7870 Activities)

Discover Target: pfk

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Txnrd1 Thioredoxin reductase 1, cytoplasmic (45279 Activities)

Discover Target: Txnrd1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

fba Putative fructose-1,6-bisphosphate aldolase (15559 Activities)

Discover Target: fba

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

FTL Ferritin light chain (43324 Activities)

Discover Target: FTL

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

crtY Lycopene cyclase (9 Activities)

Discover Target: crtY

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mechanisms of Action

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.

37 results found

Lot Number	Certificate Type	Date	Item
A2626687	Certificate of Analysis	Jan 28, 2026	I131590
A2626689	Certificate of Analysis	Jan 28, 2026	I131590
A2626690	Certificate of Analysis	Jan 28, 2026	I131590
L2519419	Certificate of Analysis	Dec 29, 2025	I131590
J2531445	Certificate of Analysis	Nov 06, 2025	I131590
J2531446	Certificate of Analysis	Nov 06, 2025	I131590
H2501062	Certificate of Analysis	Aug 12, 2025	I131590
K2027099	Certificate of Analysis	Jun 14, 2024	I131590
H2407605	Certificate of Analysis	May 21, 2024	I131590
H2407604	Certificate of Analysis	May 21, 2024	I131590
H2407608	Certificate of Analysis	May 21, 2024	I131590
E2523021	Certificate of Analysis	May 21, 2024	I131590
E2512028	Certificate of Analysis	May 21, 2024	I131590
E2406136	Certificate of Analysis	Apr 23, 2024	I131590
E2406119	Certificate of Analysis	Apr 23, 2024	I131590
E2406092	Certificate of Analysis	Apr 23, 2024	I131590
J2309571	Certificate of Analysis	Sep 07, 2023	I131590
J2309544	Certificate of Analysis	Sep 07, 2023	I131590
J2309543	Certificate of Analysis	Sep 07, 2023	I131590
L2203418	Certificate of Analysis	Nov 25, 2022	I131590
L2205007	Certificate of Analysis	Nov 25, 2022	I131590
H2311034	Certificate of Analysis	Nov 25, 2022	I131590
H2325040	Certificate of Analysis	Nov 25, 2022	I131590
B2307276	Certificate of Analysis	Nov 25, 2022	I131590
L2002051	Certificate of Analysis	Sep 19, 2022	I131590
J2022289	Certificate of Analysis	Aug 09, 2022	I131590
G2209310	Certificate of Analysis	Jun 23, 2022	I131590
G2209309	Certificate of Analysis	Jun 23, 2022	I131590
F2213199	Certificate of Analysis	Jun 15, 2022	I131590
F2222392	Certificate of Analysis	May 31, 2022	I131590
F2222383	Certificate of Analysis	May 31, 2022	I131590
G2006045	Certificate of Analysis	Apr 27, 2022	I131590
C2017167	Certificate of Analysis	Jan 19, 2022	I131590
A2221086	Certificate of Analysis	Jan 13, 2022	I131590
J2231082	Certificate of Analysis	Jan 13, 2022	I131590
J2231085	Certificate of Analysis	Jan 13, 2022	I131590
A2221087	Certificate of Analysis	Jan 13, 2022	I131590

Chemical and Physical Properties

Sensitivity	Light & Moisture Sensitive
Melt Point(°C)	95°C
Molecular Weight	184.960 g/mol
XLogP3	-0.200
Hydrogen Bond Donor Count	1
Hydrogen Bond Acceptor Count	1
Rotatable Bond Count	1
Exact Mass	184.934 Da
Monoisotopic Mass	184.934 Da
Topological Polar Surface Area	43.100 Å²
Heavy Atom Count	5
Formal Charge	0
Complexity	44.900
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

Documents & Articles

Common Reagents for Reducing Protein Disulfide Bonds

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Reducible protein Protein disulfide bond

A Practical Guide to Small-Molecule Chemical Probes: Concept Clarification, Causal Validation, and Experimental Selection (with Product Navigation and Tables A–D)

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Chemical probe Small-Molecule Chemical Probes

Endoproteinase Lys-C: Mechanism, Applications, and Method-Control Considerations for Lysine-Specific Digestion

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Peptide Mapping Serine protease Lys-C Endoproteinase Lys-C Lysine-specific cleavage Denaturing digestion LC–MS Sequence coverage Missed cleavage rate Critical peptide monitoring Method validation

Plant Omics Panorama: Workflow Frameworks and Multi-Omics Integration from Genomics to Transcriptomics, Proteomics, and Metabolomics

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Proteomics Plant omics Genomics Transcriptomics Metabolomics Multi-omics integration Phenomics Epigenomics

Bromelain: Enzymological Properties and Key Points for Food, Pharmaceutical, and Industrial Applications

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Cysteine protease bromelain proteolysis BAEE fibrin meat tenderization

Methionine: Biological Roles and Key Points for Research Application

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

glutathione one-carbon metabolism SAM Redox homeostasis methionine SAH methylation homocysteine transsulfuration pathway

Review of Chymotrypsin: Enzymological Properties, Catalytic Mechanism, and Research Applications

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Peptide Mapping Serine protease substrate specificity limited proteolysis catalytic triad Chymotrypsin Alpha-Chymotrypsin Oxyanion Hole Acyl-Enzyme Intermediate Methodological Quality Control

Clostridial Proteases: Classification, Molecular Mechanisms, and Research Applications

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

clostridial proteases

Glycoprotein Hormone Family: Molecular Features, Signaling Bias, and In Vivo Pharmacokinetics

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Glycosylation Pharmacokinetics FSH LH hCG TSH Glycoprotein hormones Common α-subunit Specific β-subunit Signaling bias

Methodological Studies on Glycoprotein Structural Characterization and Quality Attribute Analysis

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Glycosylation Glycoprotein Quality Attributes Critical Quality Attributes Released Glycan Analysis Glycopeptide Analysis Intact Mass Spectrometry Higher-Order Structure Multi-Attribute Method Comparability Study

Research Framework for Multi-Enzyme Digestion Strategies and Optimization of Proteomic Coverage

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Proteomics Mass spectrometry Multi-Enzyme Digestion Coverage Optimization Proteolytic Strategy Peptide Detectability Sample Complexity Research Framework

Thiol and Disulfide Status in Biological Samples: Detection Methods and Applications

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

glutathione disulfide bonds DTNB Thiol redox state Ellman assay protein thiol GSH/GSSG

Neuropathological Mechanisms of Cerebral Infarction

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Oxidative Stress neuroinflammation blood-brain barrier cerebral infarction ischemic stroke neuropathological mechanism ischemic penumbra excitotoxicity

Summary of Research Advances in Oxidative Stress

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

ROS Oxidative Stress Nrf2 ferroptosis non-coding RNA mitochondrial oxidative stress redox proteomic precision antioxidant therapy

Regulatory Mechanisms, Research Methods, and Modification-Omics Analysis of Protein Post-Translational Modifications

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Glycosylation methylation SUMOylation Protein Post-Translational Modifications Ubiquitination Phosphorylation Acetylation Lactylation Modification Proteomics

Why Proximity to Cysteine Does Not Necessarily Lead to Covalent Bond Formation: Warhead Reactivity, Reaction Geometry, and Target-Site Microenvironment

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Cysteine Covalent Inhibition

Citations of This Product

How to Cite Aladdin Scientific Products? Citations Search

Solution Calculators

Molarity Calculator

Determine the necessary mass, volume, or concentration for preparing a solution.

Dilution Calculator

Determine the dilution needed to prepare a stock solution.

Reconstitution Calculator

Reviews

📚 Citations by Application

Other applications52

Controlled-release & nanoparticle carrier3

Drug / compound screening21

Cell viability8

Organic synthesis — reaction medium31

Nanoparticle / material biocompatibility1

Chromatography (HPLC / GC / TLC)22

Spectroscopy sample preparation14

Topical & ophthalmic formulation2

Extraction & workup solvent39

Industrial & non-pharma application2

Cytotoxicity screening8

Cell proliferation4

Polymer synthesis & polymerization1

Cancer cell line characterization1

View all 112 citations →

Need help choosing the grade?

Our grade selection guide covers purity, stabilizer status, and application suitability for all variants in our catalog.

View Moligand™ grade guide → View Ultra pure grade guide →

Bulk & Custom Packaging Need larger quantities or custom specifications? Contact our team for a tailored quote.

Related Products

Iodoacetamide - Moligand™, ≥98% , Activator of TRPA1, CAS No.144-48-9

Iodoacetamide - Moligand™, 10mM in DMSO , Activator of TRPA1, CAS No.144-48-9

Iodoacetamide - Moligand™, Ultra pure, ≥99%(NMR) , CAS No.144-48-9

Storage & shipping

Quality documents

Literature proof

Overview

Specifications

Documentation

📋 Safety Data Sheet (SDS)

✅ Certificate of Analysis (COA)

📊 Datasheet

🔬 Specification Sheet

Advanced Data

Molarity Calculator

Dilution Calculator

Reconstitution Calculator

Customer Reviews

📚 Citations by Application

Need help choosing the grade?

View related series

Related Products