Butyl methacrylate

Butyl methacrylate is the organic compound with the formula C4H9O2CC(CH3)=CH2. A colorless liquid, it is a common monomer for the preparation of acrylate polymers.[1] It is typically polymerized under free-radical conditions.[2]

Butyl methacrylate
Names
Other names
Butyl 2-methylpropenoate, Acryester B, Acryester BMA, n-butyl methacrylate
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
ECHA InfoCard 100.002.378
EC Number
  • 202-615-1
RTECS number
  • OZ3675000
UNII
UN number 2227
Properties
C8H14O2
Molar mass 142.198 g·mol−1
Appearance colorless liquid
Density 0.8936 g/cm3
Melting point −25 °C (−13 °F; 248 K)
Boiling point 160 °C (320 °F; 433 K)
Hazards
GHS pictograms
GHS Signal word Danger
GHS hazard statements
H226, H315, H317, H319, H335
P210, P233, P240, P241, P242, P243, P261, P264, P271, P272, P280, P302+352, P303+361+353, P304+340, P305+351+338, P312, P321, P332+313, P333+313, P337+313, P362, P363, P370+378, P403+233, P403+235
NFPA 704 (fire diamond)
Flammability code 2: Must be moderately heated or exposed to relatively high ambient temperature before ignition can occur. Flash point between 38 and 93 °C (100 and 200 °F). E.g. diesel fuelHealth code 1: Exposure would cause irritation but only minor residual injury. E.g. turpentineReactivity code 2: Undergoes violent chemical change at elevated temperatures and pressures, reacts violently with water, or may form explosive mixtures with water. E.g. white phosphorusSpecial hazards (white): no code
2
1
2
Flash point 50 °C (122 °F; 323 K)
290 °C (554 °F; 563 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Health hazards

In terms of the acute toxicity of butyl methacrylate, the LD50 is 20 g/kg (oral, rat). It is an irritant to the eyes and can cause blindness.[1]

gollark: Skynet basically just lets you send messages via mine in a similar way to how modems work.
gollark: Without *someone*'s webserver, you *cannot* do cross-server communication in CC.
gollark: But it would probably be easier authentication-wise to have a dedicated HTTP/websocket server of some sort.
gollark: Skynet is the public version.
gollark: I think so.

See also

References

  1. Bauer, Jr., William (2002). "Methacrylic Acid and Derivatives". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a16_441..
  2. Granel, C.; Dubois, Ph.; Jérôme, R.; Teyssié, Ph. (1996). "Controlled Radical Polymerization of Methacrylic Monomers in the Presence of a Bis(ortho-chelated) Arylnickel(II) Complex and Different Activated Alkyl Halides". Macromolecules. 29 (27): 8576–8582. Bibcode:1996MaMol..29.8576G. doi:10.1021/ma9608380.
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.