2-Bromoacetamide - ≥98.0%(GC), high purity , CAS No.683-57-8

3 Citations
  • ≥98%(GC)
Item Number
B139173
Grouped product items
SKUSizeAvailabilityPrice Qty
B139173-5g
5g
In stock
$9.90
B139173-10g
10g
In stock
$59.90
B139173-25g
25g
In stock
$39.90
B139173-100g
100g
In stock
$125.90
View related series
amide Non heterocyclic block

Basic Description

Synonyms2-Bromoacetamide | 683-57-8 | Bromoacetamide | Acetamide, 2-bromo- | 2-Bromo-acetamide | alpha-Bromoacetamide | CHEMBL60628 | 3G598E5OYA | NSC-77371 | C2H4BrNO | NSC 77371 | BRN 1739073 | bromacetamid | bromacetamide | bromoacetoamide | bromo acetamide | 2-bromoacetoamide | 2-bromo acetam
Specifications & Purity≥98%(GC)
Shipped InNormal
Product Description

Precursor to dehydropeptidase I inactivator.

Associated Targets(Human)

ADH1A Tclin Alcohol dehydrogenase 1A (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
ADH1A Tclin Alcohol dehydrogenase (35 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Mus musculus (284745 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Rattus norvegicus (775804 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Names and Identifiers

Pubchem Sid488184372
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488184372
IUPAC Name 2-bromoacetamide
INCHI InChI=1S/C2H4BrNO/c3-1-2(4)5/h1H2,(H2,4,5)
InChi Key JUIKUQOUMZUFQT-UHFFFAOYSA-N
Canonical SMILES C(C(=O)N)Br
Isomeric SMILES C(C(=O)N)Br
WGK Germany 3
RTECS AB4587000
PubChem CID 69632
Molecular Weight 137.96
Beilstein 1739073
Reaxy-Rn 1739073

Certificates

Certificate of Analysis(COA)

Enter Lot Number to search for COA:

To view the certificate results,please click on a Lot number.For Lot numbers from past orders,please use our order status section

12 results found

Lot NumberCertificate TypeDateItem
G2213480Certificate of AnalysisApr 15, 2024 B139173
G2213523Certificate of AnalysisApr 15, 2024 B139173
G2213473Certificate of AnalysisApr 12, 2024 B139173
J2311216Certificate of AnalysisSep 26, 2023 B139173
J2311217Certificate of AnalysisSep 26, 2023 B139173
J2311222Certificate of AnalysisSep 26, 2023 B139173
J2311223Certificate of AnalysisSep 26, 2023 B139173
J1528109Certificate of AnalysisMay 10, 2023 B139173
A2125465Certificate of AnalysisDec 06, 2022 B139173
A2125464Certificate of AnalysisDec 06, 2022 B139173
E2327517Certificate of AnalysisJun 07, 2022 B139173
E2327522Certificate of AnalysisJun 07, 2022 B139173

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Chemical and Physical Properties

SolubilitySoluble in ethanol
Melt Point(°C)98℃

Safety and Hazards(GHS)

Pictogram(s) GHS06,   GHS05
Signal Danger
Hazard Statements

H301:Toxic if swallowed

H314:Causes severe skin burns and eye damage

Precautionary Statements

P280:Wear protective gloves/protective clothing/eye protection/face protection.

P321:Specific treatment (see ... on this label).

P405:Store locked up.

P501:Dispose of contents/container to ...

P264:Wash hands [and …] thoroughly after handling.

P260:Do not breathe dust/fume/gas/mist/vapors/spray.

P270:Do not eat, drink or smoke when using this product.

P301+P330+P331:IF SWALLOWED: Rinse mouth. Do NOT induce vomiting.

P304+P340:IF INHALED: Remove person to fresh air and keep comfortable for breathing.

P363:Wash contaminated clothing before reuse.

P330:Rinse mouth.

P301+P316:IF SWALLOWED: Get emergency medical help immediately.

P305+P354+P338:IF IN EYES: Immediately rinse with water for several minutes. Remove contact lenses if present and easy to do. Continue rinsing.

P302+P361+P354:IF ON SKIN: Take off Immediately all contaminated clothing. Immediately rinse with water for several minutes.

P316:Get emergency medical help immediately.

WGK Germany 3
RTECS AB4587000
Reaxy-Rn 1739073

Related Documents

Citations of This Product

1. Ni Cheng,Qi Kang,Jianhong Xiao,Na Du,Li Yu.  (2017-10-14)  Supramolecular gels: using an amide-functionalized imidazolium-based surfactant..  Journal of colloid and interface science,  511  (215-221).  [PMID:29028572]
2. Shunke Ding,Feifei Wang,Wenhai Chu,Zhongqi Cao,Yang Pan,Naiyun Gao.  (2018-07-10)  Rapid degradation of brominated and iodinated haloacetamides with sulfite in drinking water: Degradation kinetics and mechanisms..  Water research,  143  (325-333).  [PMID:29986242]
3. Dong Li, Wen Cheng, Jiehui Ren, Lu Qin, Xing Zheng, Tian Wan, Min Wang.  (2023)  In vitro toxicity assessment of haloacetamides via a toxicogenomics assay.  ENVIRONMENTAL TOXICOLOGY AND PHARMACOLOGY,  97  (104026).  [PMID:36455839]

References

1. Susanna Tchilibon,Bhalchandra V Joshi,Soo-Kyung Kim,Heng T Duong,Zhan-Guo Gao,Kenneth A Jacobson.  (2005-03-18)  (N)-methanocarba 2,N6-disubstituted adenine nucleosides as highly potent and selective A3 adenosine receptor agonists..  Journal of medicinal chemistry,  48  ((6)): (1745-1758).  [PMID:15771421]
2. George R Kracke, Monika R VanGordon, Yulia V Sevryugina, Peter J Kueffer, Kuanysh Kabytaev, Satish S Jalisatgi, M Frederick Hawthorne,.  (2014-11-26)  Carborane-derived local anesthetics are isomer dependent..  ChemMedChem,  10  ((1)): ( 62-67 ).  [PMID:25420874]
3. Lizhen Qiao,Wangjie Lv,Mengmeng Chang,Xianzhe Shi,Guowang Xu.  (2017-07-25)  Surface-bonded amide-functionalized imidazolium ionic liquid as stationary phase for hydrophilic interaction liquid chromatography..  Journal of chromatography. A,  1559  (141-148).  [PMID:28734605]
4. Ni Cheng,Qi Kang,Jianhong Xiao,Na Du,Li Yu.  (2017-10-14)  Supramolecular gels: using an amide-functionalized imidazolium-based surfactant..  Journal of colloid and interface science,  511  (215-221).  [PMID:29028572]
5. Breanne E Holmes,Lisa Smeester,Rebecca C Fry,Howard S Weinberg.  (2019-01-31)  Disinfection Byproducts Bind Human Estrogen Receptor-α..  Environmental toxicology and chemistry,  38  ((5)): (956-964).  [PMID:30698843]
6. Yunkun Qian,Yue Hu,Yanan Chen,Dong An,Paul Westerhoff,David Hanigan,Wenhai Chu.  (2020-09-01)  Haloacetonitriles and haloacetamides precursors in filter backwash and sedimentation sludge water during drinking water treatment..  Water research,  186  (116346-116346).  [PMID:32866929]
7. Y Q Wu,S Mobashery.  (1991-06-01)  Targeting renal dipeptidase (dehydropeptidase I) for inactivation by mechanism-based inactivators..  Journal of medicinal chemistry,  34  ((6)): (1914-1916).  [PMID:2061929]
8. M J Taylor,P B Dervan.  (1997-05-01)  Kinetic analysis of sequence-specific alkylation of DNA by pyrimidine oligodeoxyribonucleotide-directed triple-helix formation..  Bioconjugate chemistry,  ((3)): (354-364).  [PMID:9177841]
9. Shunke Ding,Feifei Wang,Wenhai Chu,Zhongqi Cao,Yang Pan,Naiyun Gao.  (2018-07-10)  Rapid degradation of brominated and iodinated haloacetamides with sulfite in drinking water: Degradation kinetics and mechanisms..  Water research,  143  (325-333).  [PMID:29986242]
10. Dong Li, Wen Cheng, Jiehui Ren, Lu Qin, Xing Zheng, Tian Wan, Min Wang.  (2023)  In vitro toxicity assessment of haloacetamides via a toxicogenomics assay.  ENVIRONMENTAL TOXICOLOGY AND PHARMACOLOGY,  97  (104026).  [PMID:36455839]

Solution Calculators