144932
3,4-Dichlorobenzoic acid
99%
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About This Item
Formula condensata:
Cl2C6H3CO2H
Numero CAS:
Peso molecolare:
191.01
Beilstein:
2044777
Numero CE:
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
NACRES:
NA.22
Prodotti consigliati
Livello qualitativo
Saggio
99%
Forma fisica
solid
Punto di fusione
204-206 °C (lit.)
Gruppo funzionale
carboxylic acid
chloro
Stringa SMILE
OC(=O)c1ccc(Cl)c(Cl)c1
InChI
1S/C7H4Cl2O2/c8-5-2-1-4(7(10)11)3-6(5)9/h1-3H,(H,10,11)
VPHHJAOJUJHJKD-UHFFFAOYSA-N
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Applicazioni
3,4-Dichlorobenzoic acid was employed as internal standard during the multiresidue analysis of pharmaceuticals and personal care products by ultra performance liquid chromatography-positive/negative electrospray tandem mass spectrometry. It was used to study the metabolic fate of 4-chloro-3,5-dinitrobenzoic acid.
Avvertenze
Warning
Indicazioni di pericolo
Consigli di prudenza
Classi di pericolo
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Organi bersaglio
Respiratory system
Codice della classe di stoccaggio
11 - Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
Not applicable
Punto d’infiammabilità (°C)
Not applicable
Dispositivi di protezione individuale
dust mask type N95 (US), Eyeshields, Gloves
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I clienti hanno visto anche
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Biodegradation, 9(5), 359-368 (1998)
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Analytical and bioanalytical chemistry, 391(4), 1293-1308 (2008-02-07)
The main aim of the presented research is to introduce a new technique, ultra performance liquid chromatography-positive/negative electrospray tandem mass spectrometry (UPLC-ESI/MS/MS), for the development of new simultaneous multiresidue methods (over 50 compounds). These methods were used for the determination
K Umehara et al.
Drug metabolism and disposition: the biological fate of chemicals, 28(8), 887-894 (2000-07-20)
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P Adriaens et al.
Applied and environmental microbiology, 57(1), 173-179 (1991-01-01)
When Acinetobacter sp. strain 4-CB1 was grown on 4-chlorobenzoate (4-CB), it cometabolized 3,4-dichlorobenzoate (3,4-DCB) to 3-chloro-4-hydroxybenzoate (3-C-4-OHB), which could be used as a growth substrate. No cometabolism of 3,4-DCB was observed when Acinetobacter sp. strain 4-CB1 was grown on benzoate.
Yoshiteru Noutoshi et al.
Scientific reports, 2, 705-705 (2012-10-11)
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