1,12-dodecanediol dimethacrylate profile

## 1,12-Dodecanediol Dimethacrylate: A Building Block for Research

1,12-Dodecanediol dimethacrylate (DDDM) is a **bifunctional monomer** with a long, flexible alkyl chain, and two methacrylate groups at each end. This structure makes it valuable for various research applications, particularly in the fields of **polymer chemistry, materials science, and biomedicine**.

**Here's why it's important:**

* **Crosslinking Agent:** DDDM readily undergoes **polymerization** with other monomers via a free-radical mechanism. This process allows for the formation of **crosslinked networks**, leading to the production of materials with unique properties.
* **Tailored Properties:** The length and flexibility of the alkyl chain in DDDM allow for control over the mechanical properties of the resulting polymers. For example, it can be used to synthesize **flexible and elastic materials**, suitable for applications like **soft robotics and biocompatible implants**.
* **Biocompatibility:** The long alkyl chain and the absence of potentially toxic functional groups make DDDM suitable for use in biomaterials. It can be used to create **hydrogel networks**, which are biocompatible and offer controlled release of drugs and other therapeutic agents.
* **Photopolymerization:** DDDM is compatible with **photopolymerization techniques**, allowing for the fabrication of complex structures with high spatial resolution. This enables researchers to create **microfluidic devices, 3D printed scaffolds, and other intricate structures** with potential applications in microelectronics, tissue engineering, and drug delivery.
* **Versatile Applications:** DDDM finds applications in various research areas, including:
* **Dental materials:** Used for dental fillings and restorative materials.
* **Coatings:** Offers excellent adhesion and wear resistance.
* **Adhesives:** Provides strong bonding strength and flexibility.
* **Sensors:** Used in the development of chemical and biological sensors.

**Overall, 1,12-Dodecanediol dimethacrylate's unique structural features and versatility make it a valuable tool for researchers exploring new materials and applications in various scientific disciplines.** It's a key component in the development of novel materials with enhanced properties and promising applications in numerous industries.

1,12-dodecanediol dimethacrylate: structure in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

ID Source	ID
PubMed CID	175191
SCHEMBL ID	72634
MeSH ID	M0259377

Synonym
121150-60-5
1,12-dodecanediol dimethacrylate
12-(2-methylprop-2-enoyloxy)dodecyl 2-methylprop-2-enoate
1,12-dodecanediyl bismethacrylate
2-propenoic acid, 2-methyl-, 1,12-dodecanediyl ester
einecs 276-900-4
2-propenoic acid, 2-methyl-, 1,1'-(1,12-dodecanediyl) ester
72829-09-5
dodecamethylene-dimethylacrylate
SCHEMBL72634
mfcd00080499
dodecanediol dimethacrylate
AKOS027378508
1,12-dodecanediol dimethacrylate, >/=95%,stabilized with mehq
FT-0765467
dodecane-1,12-diyl bis(2-methylacrylate)
1,12-bis(methacryloyloxy)dodecane
D5172
1,12-dodecanediol dimethacrylate (stabilized with mehq)
DTXSID501015491
D90374
BS-51193
1,12-dodecanediyl dimethacrylate
CS-0167808
1,12-dodecanedioldimethacrylate(stabilizedwithmehq)
dodecane-1,12-diylbis(2-methylacrylate)

Timeframe	Studies, This Drug (%)	All Drugs %
pre-1990	0 (0.00)	18.7374
1990's	1 (14.29)	18.2507
2000's	1 (14.29)	29.6817
2010's	5 (71.43)	24.3611
2020's	0 (0.00)	2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Publication Type	This drug (%)	All Drugs (%)
Trials	0 (0.00%)	5.53%
Reviews	0 (0.00%)	6.00%
Case Studies	0 (0.00%)	4.05%
Observational	0 (0.00%)	0.25%
Other	7 (100.00%)	84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Substance	Relationship Strength	Studies	Classes	Roles
urea pseudourea: clinical use; structure. isourea : A carboximidic acid that is the imidic acid tautomer of urea, H2NC(=NH)OH, and its hydrocarbyl derivatives.	2.06	1	isourea; monocarboxylic acid amide; one-carbon compound	Daphnia magna metabolite; Escherichia coli metabolite; fertilizer; flour treatment agent; human metabolite; mouse metabolite; Saccharomyces cerevisiae metabolite
camphor, (+-)-isomer [no description available]	2.17	1	bornane monoterpenoid; cyclic monoterpene ketone	plant metabolite
haloperidol Haloperidol: A phenyl-piperidinyl-butyrophenone that is used primarily to treat SCHIZOPHRENIA and other PSYCHOSES. It is also used in schizoaffective disorder, DELUSIONAL DISORDERS, ballism, and TOURETTE SYNDROME (a drug of choice) and occasionally as adjunctive therapy in INTELLECTUAL DISABILITY and the chorea of HUNTINGTON DISEASE. It is a potent antiemetic and is used in the treatment of intractable HICCUPS. (From AMA Drug Evaluations Annual, 1994, p279). haloperidol : A compound composed of a central piperidine structure with hydroxy and p-chlorophenyl substituents at position 4 and an N-linked p-fluorobutyrophenone moiety.	2.1	1	aromatic ketone; hydroxypiperidine; monochlorobenzenes; organofluorine compound; tertiary alcohol	antidyskinesia agent; antiemetic; dopaminergic antagonist; first generation antipsychotic; serotonergic antagonist
methacrylic acid methacrylic acid: RN given refers to parent cpd. methacrylic acid : An alpha,beta-unsaturated monocarboxylic acid that is acrylic acid in which the hydrogen at position 2 is substituted by a methyl group.	2.06	1	alpha,beta-unsaturated monocarboxylic acid
bisphenol a 4,4'-isopropylidene diphenol: stimulates proliferative responses and cytokine productions of murine spleen cells and thymus cells in vitro. bisphenol : By usage, the methylenediphenols, HOC6H4CH2C6H4OH, commonly p,p-methylenediphenol, and their substitution products (generally derived from condensation of two equivalent amounts of a phenol with an aldehyde or ketone). The term also includes analogues in the the methylene (or substituted methylene) group has been replaced by a heteroatom.. bisphenol A : A bisphenol that is 4,4'-methanediyldiphenol in which the methylene hydrogens are replaced by two methyl groups.	2.06	1	bisphenol	endocrine disruptor; environmental contaminant; xenobiotic; xenoestrogen
methylmethacrylate Methylmethacrylate: The methyl ester of methacrylic acid. It polymerizes easily to form POLYMETHYL METHACRYLATE. It is used as a bone cement.. methyl methacrylate : An enoate ester having methacrylic acid as the carboxylic acid component and methanol as the alcohol component.	2.01	1	enoate ester; methyl ester	allergen; polymerisation monomer
triethylene glycol dimethacrylate [no description available]	2.94	4
tetraethyleneglycol dimethacrylate tetraethyleneglycol dimethacrylate: structure in first source	1.98	1
mequinol mequinol: depigmenting agent; RN given refers to parent cpd	2.06	1	methoxybenzenes; phenols	metabolite
2-methyl-1,2-epoxypropane 2-methyl-1,2-epoxypropane: structure given in first source	2.1	1	epoxide
bisphenol a-glycidyl methacrylate Bisphenol A-Glycidyl Methacrylate: The reaction product of bisphenol A and glycidyl methacrylate that undergoes polymerization when exposed to ultraviolet light or mixed with a catalyst. It is used as a bond implant material and as the resin component of dental sealants and composite restorative materials.	2.42	2	diarylmethane
trimethylolpropane trimethacrylate trimethylolpropane trimethacrylate: acrylate derivative found in ultraviolet curing inks; structure in 1st source	2.1	1	carbonyl compound
camphoroquinone camphoroquinone: a natural monoterpene, non-aromatic quinone; structure given in first source. bornane-2,3-dione : A bornane monoterpenoid that is bicyclo[2.2.1]heptane substituted by methyl groups at positions 1, 7 and 7 and oxo groups at positions 2 and 3.	2.17	1	bornane monoterpenoid; carbobicyclic compound
carbamide peroxide Carbamide Peroxide: A urea peroxide compound that is commonly used in tooth whitening agents; topical anti-infective agents, and earwax remover.. urea hydrogen peroxide : A mixture obtained by combining equimolar amounts of hydrogen peroxide and urea.	2.06	1	mixture	disinfectant; oxidising agent; reagent
1,10-decanediol [no description available]	2.1	1
4-methacryloxyethyltrimellitic acid anhydride 4-methacryloxyethyltrimellitic acid anhydride: monomer used in 4-META resin; which is used as dental resin; structure given in first source; Cover-Up II is a 4-META bases bonding agent	2.01	1
pentaerythritol tetraacrylate [no description available]	2.1	1
2,2-bis-(4-(2-methacryloxyethoxy)phenyl)propane 2,2-bis-(4-(2-methacryloxyethoxy)phenyl)propane: structure given in first source	2.06	1
methacryloyloxydecyl dihydrogen phosphate methacryloyloxydecyl dihydrogen phosphate: structure given in first source	2.1	1
edba [no description available]	2.17	1	alpha-amino acid
5-(2'-naphthyl)-7-4-chlorophenyl-(2,3,6,8-tetrahydro)pyrrolo-(3,4-e)(1,4)-diazepine-6-thioxo-8-(1h,7h)one 5-(2'-naphthyl)-7-4-chlorophenyl-(2,3,6,8-tetrahydro)pyrrolo-(3,4-e)(1,4)-diazepine-6-thioxo-8-(1H,7H)one: structure given in first source	2.01	1
trimethoxysilane [no description available]	2.01	1

1,12-dodecanediol dimethacrylate

Description

Cross-References

Synonyms (26)

Research

Studies (7)

Market Indicators

Research Demand Index: 22.08

Study Types