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· · COA & SDS für jedes Produkt verfügbar · Versand am selben Tag für Lagerartikel 2-Bromoacetophenone - for GC derivatization, ≥99% , CAS No.70-11-1
GRADE & PURITY for GC derivatization ? GC-derivatization grade — reagents to make analytes GC-amenable (volatile/stable). Use before GC to derivatize polar or thermally labile compounds. ≥99% Synonyms
2-Bromoacetophenone|70-11-1|Phenacyl bromide|2-Bromo-1-phenylethanone|Bromoacetophenone|Ethanone, 2-bromo-1-phenyl-|Bromomethyl phenyl ketone|2-Bromo-1-Phenylethan-1-One|ALPHA-BROMOACETOPHENONE|omega-Bromoacetophenone|Acetophenone, 2-bromo-|Stauffer 4644|
Storage
Store at 2-8°C,Argon charged
Shipped In
Wet ice,FedEx DG Service
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Why this grade for GC derivatization, ≥99% for GC derivatization for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at 2-8°C,Argon charged Ships Wet ice,FedEx DG Service Check lot-specific COA for exact specifications.
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Quality documents SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
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Literature proof Cited in 26 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Übersicht 2-Bromoacetophenone has been used in the analysis of organic acids involving the formation of phenacyl derivatives.
Specifications Synonyme
2-Bromoacetophenone | 70-11-1 | Phenacyl bromide | 2-Bromo-1-phenylethanone | Bromoacetophenone | Ethanone, 2-bromo-1-phenyl- | Bromomethyl phenyl ketone | 2-Bromo-1-Phenylethan-1-One | ALPHA-BROMOACETOPHENONE | omega-Bromoacetophenone | Acetophenone, 2-bromo- | Stauffer 4644 |
Spezifikationen & Reinheit
for GC derivatization, ≥99%
Storage
Store at 2-8°C,Argon charged
Verschickt in
Wet ice,FedEx DG Service
Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.
Note
for GC derivatization
Namen und Kennungen Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/504751042
Kanonisches Lächeln
C1=CC=C(C=C1)C(=O)CBr
IUPAC Name
2-bromo-1-phenylethanone
InChIKey
LIGACIXOYTUXAW-UHFFFAOYSA-N
INCHI
1S/C8H7BrO/c9-6-8(10)7-4-2-1-3-5-7/h1-5H,6H2
Isomere SMILES
C1=CC=C(C=C1)C(=O)CBr
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=606474&ln=
Documentation 📋 Safety Data Sheet (SDS) Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS → ✅ 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 Kingdom Organic compounds Superclass Organic oxygen compounds Klasse Organooxygen compounds Subclass Carbonyl compounds Intermediate Tree Nodes Ketones - Aryl ketones - Phenylketones Direct Parent Alkyl-phenylketones Alternative Parents Benzoyl derivatives Aryl alkyl ketones Alpha-haloketones Organobromides Organic oxides Hydrocarbon derivatives Alkyl bromides Molecular Framework Aromatic homomonocyclic compounds Substituents Alkyl-phenylketone - Aryl alkyl ketone - Benzoyl - Benzenoid - Monocyclic benzene moiety - Alpha-haloketone - Organic oxide - Hydrocarbon derivative - Organobromide - Organohalogen compound - Alkyl halide - Alkyl bromide - Aromatic homomonocyclic compound Beschreibung This compound belongs to the class of organic compounds known as alkyl-phenylketones. These are aromatic compounds containing a ketone substituted by one alkyl group, and a phenyl group. External Descriptors alpha-bromoketone - aromatic ketone - acetophenones Data sources 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.
3D-Struktur Zugehörige Ziele (menschlich) Zugehörige Ziele (nicht menschlich) Wirkungsmechanismen Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm) Chemische und physikalische Eigenschaften Empfindlichkeit Light & Heat & Air sensitive. Brechungsindex 1.709 Flammpunkt (°F) 235.4 °F Flammpunkt (°C) 113 °C Siedepunkt (°C) 135 °C/18 mmHg Schmelzpunkt (°C) 51°C Molekulargewicht 199.040 g/mol XLogP3 2.500 Hydrogen Bond Donor Count 0 Hydrogen Bond Acceptor Count 1 Rotatable Bond Count 2 Exact Mass 197.968 Da Monoisotopic Mass 197.968 Da Topological Polar Surface Area 17.100 Ų Heavy Atom Count 10 Formal Charge 0 Complexity 116.000 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
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