DDOH
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MedKoo CAT#: 581351

CAS#: 2642-82-2

Description: DDOH is a metabolite of DDT and forms conjugates with palmitic acid in DDT-treated female rats.


Chemical Structure

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DDOH
CAS# 2642-82-2

Theoretical Analysis

MedKoo Cat#: 581351
Name: DDOH
CAS#: 2642-82-2
Chemical Formula: C14H12Cl2O
Exact Mass: 266.03
Molecular Weight: 267.149
Elemental Analysis: C, 62.94; H, 4.53; Cl, 26.54; O, 5.99

Price and Availability

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1g USD 450 2 Weeks
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Synonym: DDOH; DDOM; p,p'-Ddoh;

IUPAC/Chemical Name: 2,2-Bis(4-chlorophenyl)-1-hydroxyethane

InChi Key: ZVIDYKRNLNAXFT-UHFFFAOYSA-N

InChi Code: InChI=1S/C14H12Cl2O/c15-12-5-1-10(2-6-12)14(9-17)11-3-7-13(16)8-4-11/h1-8,14,17H,9H2

SMILES Code: OCC(C1=CC=C(Cl)C=C1)C2=CC=C(Cl)C=C2

Appearance: Solid powder

Purity: >98% (or refer to the Certificate of Analysis)

Shipping Condition: Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.

Storage Condition: Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).

Solubility: Soluble in DMSO

Shelf Life: >3 years if stored properly

Drug Formulation: This drug may be formulated in DMSO

Stock Solution Storage: 0 - 4 C for short term (days to weeks), or -20 C for long term (months).

HS Tariff Code: 2934.99.03.00

More Info:

Biological target:
In vitro activity:
In vivo activity:

Preparing Stock Solutions

The following data is based on the product molecular weight 267.15 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
Formulation protocol:
In vitro protocol:
In vivo protocol:

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8: Klotz DM, Ladlie BL, Vonier PM, McLachlan JA, Arnold SF. o,p'-DDT and its metabolites inhibit progesterone-dependent responses in yeast and human cells. Mol Cell Endocrinol. 1997 Apr 25;129(1):63-71. PubMed PMID: 9175630.

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11: Eriksson P, Nilsson-Håkansson L, Nordberg A, Aspberg A, Fredriksson A. Neonatal exposure to DDT and its fatty acid conjugate: effects on cholinergic and behavioural variables in the adult mouse. Neurotoxicology. 1990 Summer;11(2):345-54. PubMed PMID: 2234550.

12: Fawcett SC, King LJ, Bunyan PJ, Stanley PI. The metabolism of 14C-DDT, 14C-DDD, 14C-DDE and 14C-DDMU in rats and Japanese quail. Xenobiotica. 1987 May;17(5):525-38. PubMed PMID: 3604258.

13: Kujawa M, Macholz R, Knoll R, Plass R. [The enzymatic degradation of DDT. 6. The fate of the DDT metabolites dichlorodiphenyldichloroethylene and dichlorodiphenylmonochloroethylene in the rat]. Nahrung. 1987;31(3):253-7. German. PubMed PMID: 3614335.

14: Eriksson P, Nordberg A. The effects of DDT, DDOH-palmitic acid, and a chlorinated paraffin on muscarinic receptors and the sodium-dependent choline uptake in the central nervous system of immature mice. Toxicol Appl Pharmacol. 1986 Sep 15;85(2):121-7. PubMed PMID: 3764899.

15: Treinen KA, Kulkarni AP. Human placental Ca2+-ATPase: in vitro inhibition by DDT homologs. Toxicol Lett. 1986 Mar;30(3):223-9. PubMed PMID: 2939596.

16: Gold B, Brunk G. A mechanistic study of the metabolism of 1,1-dichloro-2,2-bis(p-chlorophenyl)ethane (DDD) to 2,2-bis(p-chlorophenyl)acetic acid (DDA). Biochem Pharmacol. 1984 Apr 1;33(7):979-82. PubMed PMID: 6712728.

17: Gold B, Brunk G. Metabolism of 1,1,1-trichloro-2,2-bis(p-chlorophenyl)-ethane and 1,1-dichloro-2,2-bis(p-chlorophenyl)ethane in the mouse. Chem Biol Interact. 1982 Sep;41(3):327-39. PubMed PMID: 7105253.

18: Leighty EG, Fentiman AF Jr, Thompson RM. Conjugation of fatty acids to DDT in the rat: possible mechanism for retention. Toxicology. 1980;15(2):77-82. PubMed PMID: 7376193.

19: Planche G, Croisy A, Malaveille C, Tomatis L, Bartsch H. Metabolic and mutagenicity studies on DDT and 15 derivatives. Detection of 1,1-bis(p-chlorophenyl)-2,2-dichloroethane and 1,1-bis(p-chlorophenyl)-2,2,2-trichloroethyl acetate (kelthane acetate) as mutagens in Salmonella typhimurium and of 1,1-bis(p-chlorophenyl) ethylene oxide, a likely metabolite, as an alkylating agent. Chem Biol Interact. 1979 May;25(2-3):157-75. PubMed PMID: 380827.