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1441-56-1

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1441-56-1 Usage

General Description

1,3-BUTADIENE-D6, also known as deuterated 1,3-butadiene, is a chemical compound with the molecular formula C4H6. It is an isotopologue of 1,3-butadiene, in which all six hydrogen atoms are replaced with deuterium atoms. 1,3-BUTADIENE-D6 is a highly flammable and colorless gas with a slightly sweet odor. It is commonly used as a monomer in the production of synthetic rubbers and thermoplastic elastomers, as well as in the manufacturing of plastics, resins, and other industrial chemicals. Due to its flammability and potential health hazards, proper handling and storage of 1,3-BUTADIENE-D6 is essential to ensure safety in its industrial and laboratory applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1441-56-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,4 and 1 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1441-56:
(6*1)+(5*4)+(4*4)+(3*1)+(2*5)+(1*6)=61
61 % 10 = 1
So 1441-56-1 is a valid CAS Registry Number.
InChI:InChI=1/C4H6/c1-3-4-2/h3-4H,1-2H2/i1H2,2H2,3H,4H

1441-56-1 Well-known Company Product Price

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  • Aldrich

  • (487228)  1,3-Butadiene-d6  ≥98 atom % D, ≥98% (CP), contains hydroquinone as stabilizer

  • 1441-56-1

  • 487228-1L-EU

  • 5,499.00CNY

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1441-56-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-BUTADIENE-D6

1.2 Other means of identification

Product number -
Other names perdeutero-1,3-butadiene

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:1441-56-1 SDS

1441-56-1Relevant articles and documents

Electrophilic bromination of specifically deuterated cyclohexenes: A combined experimental and theoretical investigation

Slebocka-Tilk,Neverov,Motallebi,Brown,Donini,Gainsforth,Klobukowski

, p. 2578 - 2585 (1998)

The electrophilic addition of Br2 to specifically deuterated cyclohexenes (1-5) was studied methanol (MeOH) by stopped-flow kinetics in order to determine a deuterium kinetic isotope effect (DKIE) for the various isotopomers. The DKIE for bromi

Hydrogenation of Conjugated Dienes and Isomerization of Butenes on CdO, Co3O4 and Cr2O3

Suzuki, Takashi,Tanaka, Katsumi,Toyoshima, Isamu,Okuhara, Toshio,Tanaka, Ken-ichi

, p. 1213 - 1226 (2007/10/02)

Deuteration of buta-1,3-diene, 2-methylbuta-1,3-diene and penta-1,3-diene selectively yielded but-2-ene, 2-methylbut-2-ene and 1,4-2H2>pent-2-ene on CdO and Co3O4, and but-1-ene, 2-methylbut-1-ene and 4,5-2H2>pent-2-ene on Cr2O3, respectively.These results imply that the selectivity for 1,2- and 1,4-hydrogen addition is maintained in hydrogenation of conjugated dienes, i.e. 1,4-addition on CdO and Co3O4, and 1,2-addition on Cr2O3.The hydrogenation of buta-1,3-diene using a 1:1 mixture of H2 and D2 gave 2H2>but-1-ene in larger amounts than the 2H0>isomer on Cr2O3.An isotope effect smaller than unity was interpreted by prefential adsorption of D2 on the Cr2O3 surface.Formation of 2H1>butene was dominant in deuteration of buta-1,3-diene, indicating that residual hydrogen participates in the reaction; the amount corresponded to 7 times as much as that of chemisorbed hydrogen at room temperature.Co-isomerization of 2H0> and 2H8>but-1-ene yielded, selectively, 2H0>but-2-ene on CdO.Hydrogenation of buta-1,3-diene with a 1:1:1 mixture of H2, HD and D2 also gave 2H0>butene isomers selectively on CdO.These results infer that one intermediate species for hydrogenation of buta-1,3-diene is closely related to that for isomerization of butenes, and these reactions occur through a ?-allylic anion intermediate on CdO.

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