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36038-29-6

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36038-29-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 36038-29-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,0,3 and 8 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 36038-29:
(7*3)+(6*6)+(5*0)+(4*3)+(3*8)+(2*2)+(1*9)=106
106 % 10 = 6
So 36038-29-6 is a valid CAS Registry Number.

36038-29-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name Trichloro-1-buten-3-yn

1.2 Other means of identification

Product number -
Other names 1.1.2-Trichlor-buten-(1)-in-(3)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:36038-29-6 SDS

36038-29-6Downstream Products

36038-29-6Relevant articles and documents

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 (2007/10/03)

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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