234958
1,4-Butanediol dimethacrylate
95%, contains 200-300 ppm MEHQ as inhibitor
Synonym(s):
BDDMA, Butanediol dimethacrylate, Tetramethylene methacrylate
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About This Item
Linear Formula:
[H2C=C(CH3)CO2CH2CH2-]2
CAS Number:
Molecular Weight:
226.27
EC Number:
MDL number:
UNSPSC Code:
12162002
PubChem Substance ID:
NACRES:
NA.23
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Assay
95%
form
liquid
contains
200-300 ppm MEHQ as inhibitor
refractive index
n20/D 1.456 (lit.)
bp
132-134 °C/4 mmHg (lit.)
density
1.023 g/mL at 25 °C (lit.)
storage temp.
2-8°C
SMILES string
CC(=C)C(=O)OCCCCOC(=O)C(C)=C
InChI
1S/C12H18O4/c1-9(2)11(13)15-7-5-6-8-16-12(14)10(3)4/h1,3,5-8H2,2,4H3
InChI key
XOJWAAUYNWGQAU-UHFFFAOYSA-N
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Related Categories
Application
- Formulation and polymerization of foamed 1,4-BDDMA-in-water emulsions.: This study focuses on the formulation and polymerization processes of 1,4-Butanediol dimethacrylate (1,4-BDDMA) in water emulsions, showcasing its potential in creating high-performance polymer foams suitable for various industrial applications (Dabrowski et al., 2020).
- Methacrylate-based polymer foams with controllable connectivity, pore shape, pore size and polydispersity.: The research delves into creating methacrylate-based polymer foams using 1,4-BDDMA, emphasizing its versatility in producing materials with tailored physical properties, which are crucial for biomedical and industrial uses (Dabrowski et al., 2019).
- Double Replication of Silica Colloidal Crystal Films.: This paper discusses the replication of silica colloidal crystal films using 1,4-BDDMA, highlighting its efficacy in creating structured materials for advanced technological applications (Russell and Mallouk, 2017).
- In-situ photocrosslinkable nanohybrid elastomer based on polybutadiene/polyhedral oligomeric silsesquioxane.: This study investigates the development of a nanohybrid elastomer using 1,4-BDDMA, focusing on its applications in medical device adhesives and high-performance polymer synthesis (Mirmohammadi et al., 2016).
- Effects of dental methacrylates on oxygen consumption and redox status of human pulp cells.: Research highlighting the biocompatibility and potential dental applications of 1,4-BDDMA, demonstrating its impact on human pulp cells, which is critical for dental composite materials (Nocca et al., 2014).
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
10 - Combustible liquids
WGK
WGK 1
Flash Point(F)
235.4 °F - closed cup
Flash Point(C)
113 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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Eeva K Viljanen et al.
Dental materials : official publication of the Academy of Dental Materials, 22(9), 845-851 (2005-12-29)
The aim of this study was to analyze the residual monomer content of photopolymerized dendritic methacrylate copolymers and particulate filler composites. Headspace-gas chromatography/mass spectrometry (HS-GC/MS) was compared with high performance liquid chromatography (HPLC). The resin mixtures consisted of a dendritic
M Roice et al.
Journal of protein chemistry, 20(1), 25-32 (2001-05-02)
Peptide segments corresponding to antibacterial esculentin-1 (1-15), (3344), (9-27), and their modified forms were synthesized on 1,4-butanediol dimethacrylate cross-linked polystyrene (PS-BDODMA) support. Hydroxymethyl and aminomethyl 2% PS-BDODMA supports were used for the synthesis. The HMPB linker was appended to the
Giuseppina Nocca et al.
European journal of oral sciences, 117(2), 175-181 (2009-03-27)
The polymerization of methacrylic monomers present in dental composite resins never reaches completion and therefore the leakage of residual monomers into the oral cavity and into biological fluids can cause local and systemic adverse effects. This work was carried out
Emma-Christin Lönnroth et al.
European journal of oral sciences, 111(5), 440-446 (2003-09-17)
Dental personnel and orthopedic surgeons are at risk when manually handling products containing methyl methacrylate (MMA). Dental products may also contain cross-linking agents such as ethylene glycol dimethacrylate (EGDMA) or 1,4-butanediol dimethacrylate (1,4-BDMA). Skin contact with monomers can cause hand
Aude Heloise Bonardi et al.
Macromolecular rapid communications, 40(23), e1900495-e1900495 (2019-10-31)
Photo-induced thermal polymerization upon near-infrared (NIR) light irradiation has been reported in the literature. In this approach, a component able to convert the NIR light into heat must be used in combination with a thermal initiator to initiate the free-radical
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