153168
p-Chlorophenoxyacetic acid
98%
Sinônimo(s):
4-CPA, 4-Chlorophenoxyacetic acid, CPA
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About This Item
Fórmula linear:
ClC6H4OCH2CO2H
Número CAS:
Peso molecular:
186.59
Beilstein:
1211804
Número CE:
Número MDL:
Código UNSPSC:
12352100
Produtos recomendados
Ensaio
98%
pf
157-159 °C (lit.)
cadeia de caracteres SMILES
OC(=O)COc1ccc(Cl)cc1
substituído por
Nº do produto
Descrição
Preços
Palavra indicadora
Warning
Frases de perigo
Declarações de precaução
Classificações de perigo
Acute Tox. 4 Oral
Código de classe de armazenamento
11 - Combustible Solids
Classe de risco de água (WGK)
WGK 1
Ponto de fulgor (°F)
Not applicable
Ponto de fulgor (°C)
Not applicable
Equipamento de proteção individual
dust mask type N95 (US), Eyeshields, Gloves
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Ediz Yeşilkaya et al.
Hormone research, 72(4), 225-235 (2009-09-30)
Plant growth regulators are considered to leave minimal amounts of remnants and therefore cause no significant side effects in humans. In this study, we aimed to investigate the hormonal and histopathological effects of 4-chlorophenoxy acetic acid (4-CPA), a commonly used
Oscar Moran et al.
Biochemistry, 42(18), 5176-5185 (2003-05-07)
Molecular simulation techniques were applied to predict the interaction of the CLC-0 Cl(-) channel and the channel-blocking molecule p-chlorophenoxyacetic acid (CPA). A three-dimensional model of the CLC-0 channel was constructed on the basis of the homology with the bacterial Cl(-)
Ting-Fu Jiang et al.
Analytical sciences : the international journal of the Japan Society for Analytical Chemistry, 22(6), 811-814 (2006-06-15)
A new, simple and rapid capillary electrophoresis (CE) method, using hexadimethrine bromide (HDB) as electroosmotic flow (EOF) modifier, was developed for the identification and quantitative determination of four plant hormones, including gibberellin A3 (GA3), indole-3-acetic acid (IAA), alpha-naphthaleneacetic acid (NAA)
B Lundgren et al.
Biochemical pharmacology, 36(6), 815-821 (1987-03-15)
The effects of dietary exposure to 0.125% (w/w) p-chlorophenoxyacetic acid, 2,4-dichlorophenoxyacetic acid or 2,4,5-trichlorophenoxyacetic acid on the content of peroxisomes and levels of certain xenobiotic-metabolizing enzymes in mouse liver have been investigated. In agreement with the literature on rat liver
Alessio Accardi et al.
The Journal of general physiology, 122(3), 277-293 (2003-08-13)
The Torpedo Cl- channel, CLC-0, is inhibited by clofibric acid derivatives from the intracellular side. We used the slow gate-deficient mutant CLC-0C212S to investigate the mechanism of block by the clofibric acid-derivative p-chlorophenoxy-acetic acid (CPA). CPA blocks open channels with
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