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1,2-Butadiene, 3-(ethenyloxy)-, also known as 3-(Vinyloxy)-1,2-butadiene, is an organic compound with the chemical formula C6H8O. It is a colorless liquid with a pungent odor and is soluble in organic solvents. 1,2-Butadiene, 3-(ethenyloxy)- is primarily used as a monomer in the production of various polymers, such as polybutadiene and styrene-butadiene rubber. It is also employed as a comonomer in the synthesis of copolymers with other vinyl monomers, enhancing the properties of the resulting polymers. Due to its reactivity, 1,2-butadiene, 3-(ethenyloxy)- is considered hazardous and requires proper handling and storage to prevent health and environmental risks.

4410-01-9

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4410-01-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4410-01-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,1 and 0 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4410-01:
(6*4)+(5*4)+(4*1)+(3*0)+(2*0)+(1*1)=49
49 % 10 = 9
So 4410-01-9 is a valid CAS Registry Number.

4410-01-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-ethenoxybuta-1,2-diene

1.2 Other means of identification

Product number -
Other names 1,2-Butadiene,3-(ethenyloxy)

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:4410-01-9 SDS

4410-01-9Upstream product

4410-01-9Downstream Products

4410-01-9Relevant academic research and scientific papers

HYDRATION TRIMERIZATION OF ACETYLENE IN SUPERBASIC MEDIA. II. CONDITIONS FOR THE SYNTHESIS OF 2-VINYLOXY-1,3-BUTADIENE IN THE ALKALI-DIMETHYL SULFOXIDE SYSTEM

Tarasova, O. A.,Amosova, S. V.,Istomina, S. N.,Trofimov, B. A.

, p. 1231 - 1235 (2007/10/02)

The effects of the nature and concentration of the catalyst (MOH, M = Na, K, Rb, Cs), additions (CuCl, CoCl2, NiCl2, phosphata salts), the ratio of the reagents, temperature, and the contact time on the yield and purity of 2-vinyloxy-1,3-butadiene, obtained in a single stage from acetylene and water in DMSO, were studied.It was established that the potassium hydroxide-potassium phosphate-DMSO system is the optimum system for the synthesis.By the experimental design method it was shown that increase in the C2H2:H2O ratio, increase in the concentrations of potassium hydroxide and potassium phosphate, and decrease in the reaction temperature and time have a favorable effect on the yield and purity of the product.

HYDRATION TRIMERIZATION OF ACETYLENE IN SUPERBASIC MEDIA. I. SYNTHESIS OF 2-VINYLOXY-1,3-BUTADIENE AND IDENTIFICATION OF THE SIDE PRODUCTS

Tarasova, O. A.,Amosova, S. V.,Trofimov, B. A.

, p. 1795 - 1801 (2007/10/02)

In the superbasic potassium hydroxide-dimethyl sulfoxide (DMSO) or potassium hydroxide-triethylphosphine oxide medium at 105 - 145 deg C acetylene undergoes trimerization with the capture of a water molecule to form 2-vinyloxy-1,3-butadiene with yields up to 43percent (the KOH-K3PO4-DMSO system).The following side products are formed (in DMSO): cis-vinyl 1-propenyl ether; 3-vinyloxy-1,2-butadiene; 1,2-di(vinyloxy)propane; 3-ethyl- and 4-ethyl-vinyloxybenzenes; benzene; toluene; vinyl methyl sulfide; divinyl sulfide.

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