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

71 Citations COA COA
In stock
Item Number
I131590
Grouped product items
SKU Size
Availability
 Price Qty
I131590-5g
5g
2
$38.90
I131590-25g
25g
2
$175.90
I131590-100g
100g
1
$632.90
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Bulk Order  SDS  DATASHEET  Specification Sheet

Alkylating agent.

View related series
Cell Cycle/DNA Damage (2602) DNA Alkylator/Crosslinker (72) DNA Damage (697)

Basic Description

Synonyms A808220 | Iodoacetamide, >=98.0% (AT), purum | Iodoacetamide, Single use vial of 56 mg | SCHEMBL20371 | 1219802-64-8 | PGLTVOMIXTUURA-UHFFFAOYSA- | WLN: ZV1I | BDBM50376514 | GTPL6271 | IODOACETAMIDE-D4 | NCGC00015548-06 | NCGC00093954-01 | alpha-Iodoacet
Specifications & Purity Moligand™, Ultra pure, ≥99%(NMR)
Biochemical and Physiological Mechanisms Alkylating agent used in peptide mapping because it covalently binds with thiols in cysteine residues, thereby preventing disulfide bond formation.
Storage Temp 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.
Product Description

Alkylating reagent for cysteine residues in peptide sequencing.

Taxonomic Classification

Taxonomy Tree

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

Associated Targets(Human)

CYP3A4 Tclin Cytochrome P450 3A4 (1 Activities)
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)
Activity Type Activity Value -log(M) Mechanism of Action Activity Reference Publications (PubMed IDs)
TYMS Tclin Thymidylate synthase (1651 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CHRM1 Tclin Muscarinic acetylcholine receptor M1 (12690 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
VDR Tclin Vitamin D receptor (26531 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
AK2 Tbio Adenylate kinase 2 (264 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
POLB Tchem DNA polymerase beta (23632 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
GLA Tclin Alpha-galactosidase A (5444 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ARSA Tbio Cerebroside-sulfatase (655 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ALOX15B Tchem Arachidonate 15-lipoxygenase, type II (7244 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CYP2D6 Tclin Cytochrome P450 2D6 (33882 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ALOX15 Tchem Arachidonate 15-lipoxygenase (7108 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CYP1A2 Tchem Cytochrome P450 1A2 (26471 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CYP2C9 Tchem Cytochrome P450 2C9 (32119 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CYP2C19 Tchem Cytochrome P450 2C19 (29246 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
TP53 Tchem Cellular tumor antigen p53 (48468 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
F13A1 Tchem Coagulation factor XIII (223 Activities)
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)
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)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
KDM4E Tchem Lysine-specific demethylase 4D-like (40243 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
USP2 Tbio Ubiquitin carboxyl-terminal hydrolase 2 (8818 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
LMNA Tbio Prelamin-A/C (36751 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
RECQL Tbio ATP-dependent DNA helicase Q1 (5575 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
BLM Tchem Bloom syndrome protein (4248 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HPGD Tchem 15-hydroxyprostaglandin dehydrogenase [NAD+] (24926 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
THPO Tbio Thrombopoietin (834 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
GMNN Tbio Geminin (128009 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
PMP22 Tbio Peripheral myelin protein 22 (699 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CBX1 Tbio Chromobox protein homolog 1 (92434 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
MPHOSPH8 Tbio M-phase phosphoprotein 8 (656 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ATG4B Tchem Cysteine protease ATG4B (985 Activities)
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)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ADH1A Tclin Alcohol dehydrogenase (35 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Associated Targets(non-human)

Saccharomyces cerevisiae (19171 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Rattus norvegicus (775804 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
GCN5 Histone acetyltransferase GCN5 (89 Activities)
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)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
pfk 6-phospho-1-fructokinase (7870 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Txnrd1 Thioredoxin reductase 1, cytoplasmic (45279 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
fba Putative fructose-1,6-bisphosphate aldolase (15559 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
FTL Ferritin light chain (43324 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
crtY Lycopene cyclase (9 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

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 504750705
Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504750705
IUPAC Name 2-iodoacetamide
INCHI InChI=1S/C2H4INO/c3-1-2(4)5/h1H2,(H2,4,5)
InChIKey PGLTVOMIXTUURA-UHFFFAOYSA-N
Smiles C(C(=O)N)I
Isomeric SMILES C(C(=O)N)I
WGK Germany 3
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=

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.

30 results found

Lot Number Certificate Type Date Item
H2325040 Certificate of Analysis May 13, 2025 I131590
H2311034 Certificate of Analysis May 13, 2025 I131590
L2205007 Certificate of Analysis Sep 06, 2024 I131590
E2523021 Certificate of Analysis May 21, 2024 I131590
H2407604 Certificate of Analysis May 21, 2024 I131590
H2407605 Certificate of Analysis May 21, 2024 I131590
H2407608 Certificate of Analysis May 21, 2024 I131590
E2512028 Certificate of Analysis May 21, 2024 I131590
E2406092 Certificate of Analysis Apr 23, 2024 I131590
E2406119 Certificate of Analysis Apr 23, 2024 I131590
E2406136 Certificate of Analysis Apr 23, 2024 I131590
J2309543 Certificate of Analysis Sep 07, 2023 I131590
J2309544 Certificate of Analysis Sep 07, 2023 I131590
J2309571 Certificate of Analysis Sep 07, 2023 I131590
L2203418 Certificate of Analysis Nov 25, 2022 I131590
B2307276 Certificate of Analysis Nov 25, 2022 I131590
L2002051 Certificate of Analysis Sep 19, 2022 I131590
K2027099 Certificate of Analysis Sep 16, 2022 I131590
J2022289 Certificate of Analysis Aug 09, 2022 I131590
G2209309 Certificate of Analysis Jun 23, 2022 I131590
G2209310 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
J2231085 Certificate of Analysis Jan 13, 2022 I131590
A2221087 Certificate of Analysis Jan 13, 2022 I131590
J2231082 Certificate of Analysis Jan 13, 2022 I131590
A2221086 Certificate of Analysis Jan 13, 2022 I131590

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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 Ų
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

Citations of This Product

How to Cite Aladdin Scientific Products?
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14. Erdong Yuan, Miao Zhou, Zhengyang Liang, William Kwame Amakye, Chuanli Hou, Jiaoyan Ren.  (2023)  Effect of sturgeon protein in promoting the adhesion of Lactobacillus plantarum and Lactobacillus rhamnosus.  Food Bioscience,  54  (102863). 
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29. Muhammad Mujahid Ali, Zhiyuan Zhu, Dilshad Hussain, Zhengchao Shen, Yutian He, Zhenxia Du.  (2021)  Flexible and hierarchical metal-organic framework composite as solid-phase media for facile affinity-tip fabrication to selectively enrich glycopeptides and phosphopeptides.  TALANTA,  233  (122576). 
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31. He Qi, Zheng Li, Haijiao Zheng, Qiong Jia.  (2021)  Carnosine functionalized magnetic metal–organic framework nanocomposites for synergistic enrichment of phosphopeptides.  ANALYTICA CHIMICA ACTA,  1157  (338383). 
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38. Weigui Luo, Yuan Xiao, Qiwen Liang, Yi Su, Langtao Xiao.  (2019)  Identification of Potential Auxin-Responsive Small Signaling Peptides through a Peptidomics Approach in Arabidopsis thaliana.  MOLECULES,  24  (17): (3146). 
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