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Bisphenol A glycerolate dimethacrylate - reagent grade, high purity , CAS No.1565-94-2

In stock
Item Number
B106764
Grouped product items
SKU Size
Availability
Price Qty
B106764-5ml
5ml
5
$24.90
B106764-25ml
25ml
10
$87.90
B106764-100ml
100ml
4
$281.90
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Basic Description

Synonyms 2,2-bis(4-(2-hydroxy-3-methacryloxypropoxy)phenyl)propane | BISPHENOL A-GLYCIDYL METHACRYLATE | Bis-gma | Bisphenol A glycerolate dimethacrylate | Bisphenol A Glycidyl Methacrylate | Bisphenol A glycidylmethacrylate | Silux | [2-hydroxy-3-[4-[2-[4-[2-hydr
Specifications & Purity Reagent grade
Storage Temp Store at 2-8°C,Protected from light
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Grade Reagent Grade
Product Description

Bisphenol A glycerolate dimethacrylate(BisGMA) is an advanced derivative of Bisphenol A(BPA). It is a conventional epoxy methacrylate that is widely used as a monomer in many applications due to the following properties:
Phenyl ring provides chemical resistance
Ether linkage allows flexibility
Hydroxyl group gives good adhesion
Methacrylate is the reactive site for crosslinking


Application:

The Progress in Development of Dental Restorative Materials
Bisphenol A glycerolate dimethacrylate can be used:
As a crosslinking monomer in the preparation of zwitter ionic monolithic columns for liquid chromatography.
In the preparation of an antibacterial dental adhesive.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Benzenoids
Class Benzene and substituted derivatives
Subclass Diphenylmethanes
Intermediate Tree Nodes Not available
Direct Parent Diphenylmethanes
Alternative Parents Phenylpropanes  Phenoxy compounds  Phenol ethers  Alkyl aryl ethers  Dicarboxylic acids and derivatives  Enoate esters  Secondary alcohols  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular Framework Aromatic homomonocyclic compounds
Substituents Diphenylmethane - Phenylpropane - Phenoxy compound - Phenol ether - Alkyl aryl ether - Dicarboxylic acid or derivatives - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Carboxylic acid ester - Secondary alcohol - Carboxylic acid derivative - Ether - Hydrocarbon derivative - Organic oxide - Alcohol - Carbonyl group - Organooxygen compound - Organic oxygen compound - Aromatic homomonocyclic compound
Description This compound belongs to the class of organic compounds known as diphenylmethanes. These are compounds containing a diphenylmethane moiety, which consists of a methane wherein two hydrogen atoms are replaced by two phenyl groups.
External Descriptors diarylmethane

Associated Targets(Human)

TSHR Tclin Thyroid stimulating hormone receptor (29986 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
PTH1R Tclin Parathyroid hormone receptor (47172 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
GLP1R Tclin Glucagon-like peptide 1 receptor (111429 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
POLH Tchem DNA polymerase eta (21678 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
SNCA Tchem Alpha-synuclein (10960 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
GMNN Tbio Geminin (128009 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ATAD5 Tbio ATPase family AAA domain-containing protein 5 (122566 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ATXN2 Tbio Ataxin-2 (54410 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Associated Targets(non-human)

ampC Beta-lactamase AmpC (62480 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Plasmodium falciparum (966862 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
INS1 (2867 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

Pubchem Sid 488182090
Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488182090
IUPAC Name [2-hydroxy-3-[4-[2-[4-[2-hydroxy-3-(2-methylprop-2-enoyloxy)propoxy]phenyl]propan-2-yl]phenoxy]propyl] 2-methylprop-2-enoate
INCHI InChI=1S/C29H36O8/c1-19(2)27(32)36-17-23(30)15-34-25-11-7-21(8-12-25)29(5,6)22-9-13-26(14-10-22)35-16-24(31)18-37-28(33)20(3)4/h7-14,23-24,30-31H,1,3,15-18H2,2,4-6H3
InChIKey AMFGWXWBFGVCKG-UHFFFAOYSA-N
Smiles CC(=C)C(=O)OCC(COC1=CC=C(C=C1)C(C)(C)C2=CC=C(C=C2)OCC(COC(=O)C(=C)C)O)O
Isomeric SMILES CC(=C)C(=O)OCC(COC1=CC=C(C=C1)C(C)(C)C2=CC=C(C=C2)OCC(COC(=O)C(=C)C)O)O
WGK Germany 1
RTECS UD3438000
Molecular Weight 512.59
Reaxy-Rn 2316426
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2316426&ln=

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

38 results found

Lot Number Certificate Type Date Item
F2505229 Certificate of Analysis May 29, 2025 B106764
F2505263 Certificate of Analysis May 29, 2025 B106764
F2505264 Certificate of Analysis May 29, 2025 B106764
D2503532 Certificate of Analysis Mar 31, 2025 B106764
D2511681 Certificate of Analysis Mar 31, 2025 B106764
D2514532 Certificate of Analysis Mar 21, 2025 B106764
A2306258 Certificate of Analysis Feb 17, 2025 B106764
K2406295 Certificate of Analysis Oct 23, 2024 B106764
K2406632 Certificate of Analysis Oct 23, 2024 B106764
K2406633 Certificate of Analysis Oct 23, 2024 B106764
K2406335 Certificate of Analysis Oct 23, 2024 B106764
A2306283 Certificate of Analysis Oct 15, 2024 B106764
A2306503 Certificate of Analysis Oct 15, 2024 B106764
J2228198 Certificate of Analysis Aug 09, 2024 B106764
G2424302 Certificate of Analysis Jun 29, 2024 B106764
G2424408 Certificate of Analysis Jun 29, 2024 B106764
B2505030 Certificate of Analysis Jun 29, 2024 B106764
F2406133 Certificate of Analysis Jun 01, 2024 B106764
F2406245 Certificate of Analysis Jun 01, 2024 B106764
F2406134 Certificate of Analysis Jun 01, 2024 B106764
D2222130 Certificate of Analysis Jan 22, 2024 B106764
I2305056 Certificate of Analysis Aug 22, 2023 B106764
I2305057 Certificate of Analysis Aug 22, 2023 B106764
I2306167 Certificate of Analysis Aug 22, 2023 B106764
I2306164 Certificate of Analysis Aug 22, 2023 B106764
C2307942 Certificate of Analysis Jan 31, 2023 B106764
C2307938 Certificate of Analysis Jan 31, 2023 B106764
A2306253 Certificate of Analysis Dec 14, 2022 B106764
A2306312 Certificate of Analysis Dec 14, 2022 B106764
K2226251 Certificate of Analysis Nov 19, 2022 B106764
K2226257 Certificate of Analysis Nov 19, 2022 B106764
J2228232 Certificate of Analysis Oct 19, 2022 B106764
J2228191 Certificate of Analysis Oct 19, 2022 B106764
H2231139 Certificate of Analysis Aug 17, 2022 B106764
H2231160 Certificate of Analysis Aug 17, 2022 B106764
H2231099 Certificate of Analysis Aug 17, 2022 B106764
D2222131 Certificate of Analysis Mar 26, 2022 B106764
D2222132 Certificate of Analysis Mar 26, 2022 B106764

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Chemical and Physical Properties

Sensitivity Light sensitive;air sensitive;heat sensitive
Refractive Index 1.552
Flash Point(°C) 110°C
Molecular Weight 512.600 g/mol
XLogP3 5.100
Hydrogen Bond Donor Count 2
Hydrogen Bond Acceptor Count 8
Rotatable Bond Count 16
Exact Mass 512.241 Da
Monoisotopic Mass 512.241 Da
Topological Polar Surface Area 112.000 Ų
Heavy Atom Count 37
Formal Charge 0
Complexity 698.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 2
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 1

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1. Z. Xu, Q. Zhang, Q. Ji, X. Gao, G. Chen, S. Xie, G. Cai, Y. Shen, L. Chen, J. Sun, Z. Yang, L. Chen, Y.-J. Cheng, P. Müller-Buschbaum, Y. Xia.  (2023)  Facile scalable multilevel structure engineering makes Ti0.667Nb1.333O4 a new promising lithium-ion battery anode.  Materials Today Sustainability,  24  (100521). 
2. Lu Shuxin, Zhang Hongyu, Chai Maozhou, Yao Xiaohong, Zhang Xiangyu, Yang Yongqiang.  (2023)  Mechanical and antibacterial properties of resin co-filled with mesoporous silica and graphene quantum dots.  Carbon Letters,  33  (2): (373-385). 
3. Wang Yuhe, Luo Shao-hua, Dou Yuxin, Zhang Xian, Wang Zihan, Yan Shengxue, Wang Luoxuan, Wang Xuan, Wu Haiyan, Chen Yingying.  (2022)  Preparation and mechanical properties of polymer infiltrated feldspar ceramic for dental restoration materials.  JOURNAL OF POLYMER RESEARCH,  29  (11): (1-8). 
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5. Zonghua Wang, Xiaoran Zhang, Shuo Yao, Jiaxin Zhao, Chuanjian Zhou, Junling Wu.  (2022)  Development of low-shrinkage dental adhesives via blending with spiroorthocarbonate expanding monomer and unsaturated epoxy resin monomer.  Journal of the Mechanical Behavior of Biomedical Materials,  133  (105308). 
6. Jing Cao, Dan-Lei Yang, Dan Wang, Jie-Xin Wang.  (2022)  Spray-drying-assisted fabrication of CaF2/SiO2 nanoclusters for dental restorative composites.  DENTAL MATERIALS,  38  (835). 
7. Niu Hao, Yang Dan-Lei, Pu Yuan, Wang Dan, Wang Jie-Xin.  (2022)  Computational and experimental study of dental resin composites with high filler content.  JOURNAL OF MATERIALS SCIENCE,  57  (10): (5788-5804). 
8. Xiaoyan Wang, Ya-Jun Cheng, Suzhe Liang, Qing Ji, Jin Zhu, Yonggao Xia.  (2022)  Ultrafine SnO2/Sn Nanoparticles Embedded into an In Situ Generated Meso-/Macroporous Carbon Matrix with a Tunable Pore Size.  LANGMUIR,  38  (5): (1689–1697). 
9. Qiting Huang, Zelin Liang, Junda Li, Ying Bai, Jingwei He, Zhengmei Lin.  (2021)  Size Dependence of Particulate Calcium Phosphate Fillers in Dental Resin Composites.  ACS Omega,  (50): (35057–35066). 
10. Xiaofeng Wang, Yongfeng Chen, Runze Yu, Ruiqiang Wang, Zhixiang Xu.  (2021)  A sensitive biomimetic enzyme-linked immunoassay method based on Au@Pt@Au composite nanozyme label and molecularly imprinted biomimetic antibody for histamine detection.  FOOD AND AGRICULTURAL IMMUNOLOGY,  32  (1): (592-605). 
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13. Suzhe Liang, Ya-Jun Cheng, Xiaoyan Wang, Zhuijun Xu, Liujia Ma, Hewei Xu, Qing Ji, Xiuxia Zuo, Peter Müller-Buschbaum, Yonggao Xia.  (2021)  Impact of CO2 activation on the structure, composition, and performance of Sb/C nanohybrid lithium/sodium-ion battery anodes.  Nanoscale Advances,  (7): (1942-1953). 
14. Dan-Lei Yang, Ya-Nan Cui, Qian Sun, Mei Liu, Hao Niu, Jie-Xin Wang.  (2021)  Antibacterial activity and reinforcing effect of SiO2–ZnO complex cluster fillers for dental resin composites.  Biomaterials Science,  (5): (1795-1804). 
15. Hao Niu, Dan-Lei Yang, Qian Sun, Yuan Pu, Tianyu Gao, Jie-Xin Wang.  (2020)  A new method for predicting the maximum filler loading of dental resin composites based on DEM simulations and experiments.  DENTAL MATERIALS,  36  (e375). 
16. Han-Ping Yu, Ying-Jie Zhu, Zhi-Chao Xiong, Bing-Qiang Lu.  (2020)  Bioinspired fiberboard-and-mortar structural nanocomposite based on ultralong hydroxyapatite nanowires with high mechanical performance.  CHEMICAL ENGINEERING JOURNAL,  399  (125666). 
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18. Dan-Lei Yang, Qian Sun, Yong-Hong Duan, Hao Niu, Rui-Li Wang, Dan Wang, Mei-Fang Zhu, Jie-Xin Wang.  (2019)  Efficient Construction of SiO2 Colloidal Nanoparticle Clusters as Novel Fillers by a Spray-Drying Process for Dental Composites.  INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH,  58  (39): (18178–18186). 
19. Cui Ben-Cang, Li Jing, Lin Yuan-Hua, Shen Yang, Li Ming, Deng Xu-Liang, Nan Ce-Wen.  (2019)  Polymer-infiltrated layered silicates for dental restorative materials.  RARE METALS,  38  (11): (1003-1014). 
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22. Han-Ping Yu, Ying-Jie Zhu, Bing-Qiang Lu.  (2019)  Dental enamel-mimetic large-sized multi-scale ordered architecture built by a well controlled bottom-up strategy.  CHEMICAL ENGINEERING JOURNAL,  360  (1633). 
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25. Wang Huining, Cui Bencang, Li Jing, Li Shu, Lin Yuanhua, Liu Deping, Li Ming.  (2017)  Mechanical properties and biocompatibility of polymer infiltrated sodium aluminum silicate restorative composites.  Journal of Advanced Ceramics,  (1): (73-79). 
26. Ze Zhang, Ye-Zi You, De-Cheng Wu, Chun-Yan Hong.  (2015)  A novel multicomponent reaction and its application in sequence-ordered functional polymer synthesis.  POLYMER,  64  (221). 
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