399361
6-Oxoheptanoic acid
technical grade, 90%
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About This Item
Formula condensata:
CH3CO(CH2)4CO2H
Numero CAS:
Peso molecolare:
144.17
Numero CE:
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
NACRES:
NA.22
Prodotti consigliati
Grado
technical grade
Livello qualitativo
Saggio
90%
Forma fisica
solid
P. eboll.
158-162 °C/9 mmHg (lit.)
Punto di fusione
35-37 °C (lit.)
Densità
1.059 g/mL at 25 °C (lit.)
Gruppo funzionale
carboxylic acid
ketone
Stringa SMILE
CC(=O)CCCCC(O)=O
InChI
1S/C7H12O3/c1-6(8)4-2-3-5-7(9)10/h2-5H2,1H3,(H,9,10)
IZOQMUVIDMLRDC-UHFFFAOYSA-N
Categorie correlate
Descrizione generale
6-Oxoheptanoic acid is a monocarboxylic acid with acyl functional group. Mass spectrometric characterization of 6-oxoheptanoic acid by electrospray ionization coupled to a triple quadrupole and TOF analyzer hybrid system has been reported.
Applicazioni
6-Oxoheptanoic acid may be used in the following studies:
- As ketone linker used for the conjugation of hydrazide derivatives to proteins.
- Synthesis of N-(2-propynyl)-6-oxoheptanamide.
- Synthesis of adenosine triphosphate derivative.
Avvertenze
Danger
Indicazioni di pericolo
Classi di pericolo
Eye Dam. 1 - Skin Corr. 1B
Codice della classe di stoccaggio
8A - Combustible corrosive hazardous materials
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
235.4 °F - closed cup
Punto d’infiammabilità (°C)
113 °C - closed cup
Dispositivi di protezione individuale
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
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Mass spectrometric characterization of small oxocarboxylic acids and gas phase ion fragmentation mechanisms studied by electrospray triple quadrupole-MS/MS-TOF system and DFT theory.
Kanawati B, et al.
International Journal of Mass Spectrometry, 266(1), 97-113 (2007)
A Safavy et al.
Bioconjugate chemistry, 10(1), 18-23 (1999-01-20)
A procedure utilizing an activated ester approach for conjugation of unprotected hydroxamic acids to antibodies and peptides was recently reported. Here, an alternative method with advantages over the activated ester strategy is described. This protocol utilizes the hydrazone formation between
Synthesis of methylketone containing nucleoside triphosphates for RNA labelling
Trevisiol E, et al.
Tetrahedron, 56(35), 6501-6510 (2000)
Erik Selander et al.
Proceedings of the National Academy of Sciences of the United States of America, 112(20), 6395-6400 (2015-04-29)
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