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1,2,3,4-Tetrachlorobuta-1,3-diene (also known as (E,E)-1,2,3,4-tetrachlorobutadiene) is a reductive dechlorination product of hexachloro-1,3-butadiene, primarily formed under methanogenic conditions in anaerobic environments such as Rhine River sediment. It is the major transformation product (>90%) of hexachloro-1,3-butadiene degradation, with minor traces of trichloro-1,3-butadiene isomers also detected. The formation of 1,2,3,4-tetrachlorobuta-1,3-diene is attributed to microbial activity in sediment systems, whereas abiotic model systems with hydroxocobalamin and titanium(III) citrate yield different degradation products.

18149-76-3

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18149-76-3 Usage

Physical state

Colorless to yellow liquid

Solubility

Insoluble in water

Odor

Sweet

Uses

Intermediate in the production of other chemicals

Byproduct

Chlorination of hydrocarbons

Environmental hazard

Potential environmental hazard

Human health concern

Toxic properties and ability to persist in the environment

Classification

Substance that may cause cancer

Regulation

Regulated by various environmental and health agencies

Check Digit Verification of cas no

The CAS Registry Mumber 18149-76-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,1,4 and 9 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 18149-76:
(7*1)+(6*8)+(5*1)+(4*4)+(3*9)+(2*7)+(1*6)=123
123 % 10 = 3
So 18149-76-3 is a valid CAS Registry Number.

18149-76-3Relevant academic research and scientific papers

Comparison of Reductive Dechlorination of Hexachloro-1,3-butadiene in Rhine Sediment and Model Systems with Hydroxocobalamin

Bosma, Tom N. P.,Cottaar, Francis H. M.,Posthumus, Maarten A.,Teunis, Cees J.,Veldhuizen, Albertus van,et al.

, p. 1124 - 1128 (1994)

Transformations of hexachloro-1,3-butadiene were studied in columns packed with Rhine River sediment and in batch incubations containing titanium(III) citrate and hydroxocobalamin. Columns were operated under various redox conditions. Transformation was observed in a methanogenic column at influent concentrations of 4 and 400 nmol/L but not in columns where oxygen or nitrate were fed as terminal electron acceptors. Hexachloro-1,3-butadiene was reductively dechlorinated to (E,E)-1,2,3,4-tetrachlorobutadiene (> 90 percent) and traces of a trichloro-1,3-butadiene isomer ( 5 percent). (E)-1,1,2,3,4-Pentachloro-1,3-butadiene was detected as intermediary product. Reductive dechlorination in the column was ascribed to the activity of anaerobic microorganisms. In the batch experiments with titanium(III) citrate and hydroxocobalamin, hexachloro-1,3-butadiene (5 and 500 μmol/L) was transformed to an isomer of pentachloro-1,3-butadiene and two compounds with molar masses of 154 and 52, tentatively identified as trichloro-1-buten-3-yn, and 1-buten-3-yn respectively.

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