Polychloroprene

HCID 178599209CAS 9010-98-4

Basic information

Standard SMILES
C=CC(=C)Cl
InChIKey
YACLQRRMGMJLJV-UHFFFAOYSA-N
Molecular formula
C4H5Cl
Average molar mass
88.5355 g/mol

Names & identifiers

Preferred name
Polychloroprene
English name
Polychloroprene
Molecular formula
C4H5Cl
Molecular weight
88.5355

Names & synonyms

neopreneCR244CHLOROPRENE RESINpoly(2-chlorobutadiene)POLY(2-CHLORO-1,3-BUTADIENE)gr-mfs651TS808TS919TS809

Database identifiers

CAS
9010-98-4

Properties

Physicochemical properties

Melting point
260 °C · >260 °C
Density
1.23 g/mL · 1.23 g/mL at 25 °C(lit.)
storage temp.
-196 °C · -196°C
form
chunks
color
White to beige
Viscosity
40 Mooney · 40Mooney(lit.)

Safety & regulation

Safety data

PPE
Eyeshields, Gloves, type N95 (US)
wgk
3
tsca
TSCA listed
rtecs
EI9640000
safety_code
24/25
Storage Class
11 - Combustible Solids

Chemistry & industry

Applications · 3 items

DescriptionNeoprene, also known as polychloroprene and chloroprene rubber, is an elastomer produced by polymerization of chloroprene.

HistoryPolychloroprene was discovered in 1930 at E. I. DuPont de Nemours & Co. inWilmington Delaware. The discovery grew out of a need to develop a synthetic substitute for natural rubber. DuPont first marketed this first commercially successful synthetic elastomer as DuPrene in 1933. In response to new technology development that significantly improved the product and manufacturing process, the name was changed to Neoprene in 1936. The current commercially acceptable generic name for this class of chlorinated elastomers is CR or chloroprene rubber. polychloroprene structure

UsesPolychloroprene is a (Solid) Mechanical rubber products, lining oil-loading hose and reaction equipment, adhesive cement, binder for rocket fuels, coatings for electric wiring, gaskets and seals. (Liquid) Specialty items made by dipping or electrophoresis from the latex. (Foam) Adhesive tape to replace metal fasteners for automotive accessories, seat cushions, carpet backing, sealant

Preparation methods · 1 item

PreparationPolychloroprene is made from one of two starting materials, acetylene or butadiene. Acetylene can be dimerized and then chloronated to form chloroprene. Alternatively, when adequate butadiene is available, this can be directly halogenated (eqs. 7 and 8). In either case, the chloroprene product can then be polymerized to polychloroprene. Essentially a butadiene elastomer with chlorine present in the backbone,the polymer exhibits excellent tensile strength and low hysteresis, much like natural rubber. Tensile strength properties up to 28 MPa are possible with the proper reinforcing system (see FILLERS). The polarity imparted by the chlorine atom improves the oil and solvent resistance approaching those of nitrile polymers. The polymer can be protected with para-phenylenediamine antiozonants to give ozone resistance, and heat aging is also good. As a result, chloroprene elastomers are used in a wide variety of applications needing a balance of such properties.

Suppliers50 total

湖北永阔科技有限公司027-59223108 15972152991 · [email protected]
湖北万得化工有限公司15377098680 15377098680 · [email protected]
上海钰博生物科技有限公司021-60514606 18321282235 · [email protected]
郑州裕和食品添加剂有限公司0371-56060979 13838386843
江苏艾康生物医药研发有限公司025-66061636 19370895928 · [email protected]

Additional notes

DefinitionChEBI: A macromolecule composed of repeating (2Z)-2-chlorobut-2-ene-1,4-diyl units.

Related reactions

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Linked notes

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