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100870

Sigma-Aldrich

Bis(4-chlorophenyl)acetic acid

98%

Synonym(s):

4,4′-DDA

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About This Item

Linear Formula:
(ClC6H4)2CHCO2H
CAS Number:
Molecular Weight:
281.13
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:

Assay

98%

mp

167-169 °C (lit.)

SMILES string

OC(=O)C(c1ccc(Cl)cc1)c2ccc(Cl)cc2

InChI

1S/C14H10Cl2O2/c15-11-5-1-9(2-6-11)13(14(17)18)10-3-7-12(16)8-4-10/h1-8,13H,(H,17,18)

InChI key

YIOCIFXUGBYCJR-UHFFFAOYSA-N

Pictograms

Health hazardExclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Carc. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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M Kujawa et al.
Die Nahrung, 31(3), 253-257 (1987-01-01)
DDE is hydrogenated in the rat organism. The distribution of the compound is described. DDMU is degradated to DBP as well as transformed to DDA and DDOH. Excretion and distribution are studied.
M A Dawson et al.
The Journal of pharmacology and experimental therapeutics, 266(2), 673-677 (1993-08-01)
We assessed the interaction of several pesticides with renal organic anion transport based on inhibition of the active transepithelial transport of p-aminohippuric acid ([3H]PAH) by primary cultures of winter flounder proximal tubules. Four structurally similar chlorophenoxy acid herbicides were tested.
L A Hilgers et al.
International archives of allergy and applied immunology, 80(3), 320-325 (1986-01-01)
Modulation of delayed-type hypersensitivity reaction (DTH) in mice by synthetic adjuvants and the mode of their action were investigated. Intracutaneous injection of azobenzenearsonate coupled to phosphatidylethanolamine (A-PE) without adjuvant did not induce DTH. Administration of A-PE with the quaternary amines
Karsten Hemmrich et al.
Cytotherapy, 12(4), 547-553 (2010-04-08)
Obesity is correlated with chronic low-grade inflammation. Thus the induction of inflammation could be used to stimulate adipose tissue formation in tissue-engineering approaches. As nitric oxide (NO) is a key regulator of inflammation, we investigated the effect of NO and
W K Nichols et al.
Drug metabolism and disposition: the biological fate of chemicals, 23(5), 595-599 (1995-05-01)
Isolated rabbit Clara cells and a transformed human bronchial epithelial cell line, BEAS-2B, were used to investigate the mechanism of cytotoxicity of 1,1-dichloro-2,2-bis(p-chlorophenyl)ethane (DDD), a persistent insecticide and stable metabolite of 1,1,1-trichloro-2,2- bis(p-chlorophenyl)ethane. Both BEAS-2B cells and rabbit Clara cells

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