246832
Tri(propylene glycol) diacrylate, mixture of isomers
contains MEHQ and HQ as inhibitors, technical grade
Sinónimos:
TRPGDA
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Fórmula lineal:
H2C=CHCO(OC3H6)3O2CCH=CH2
Número CAS:
Peso molecular:
300.35
MDL number:
UNSPSC Code:
12162002
PubChem Substance ID:
EC Number:
256-032-2
NACRES:
NA.23
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Permítanos ayudarleInChI
1S/C15H24O6/c1-6-14(16)20-12(4)9-18-8-11(3)19-10-13(5)21-15(17)7-2/h6-7,11-13H,1-2,8-10H2,3-5H3
InChI key
ZDQNWDNMNKSMHI-UHFFFAOYSA-N
SMILES string
CC(COC(C)COC(=O)C=C)OCC(C)OC(=O)C=C
grade
technical grade
vapor density
>1 (vs air)
vapor pressure
<0.01 mmHg ( 20 °C)
form
liquid
contains
150-220 ppm monomethyl ether hydroquinone and hydroquinone (total inhibitor)
refractive index
n20/D 1.45 (lit.)
density
1.03 g/mL at 25 °C (lit.)
Quality Level
Categorías relacionadas
General description
Tri(propylene glycol) diacrylate (TPGDA) is a multifunctional acrylate monomer characterized by its high reactivity and ability to polymerize rapidly under UV or thermal initiation. Its structure includes multiple acrylate groups, which contribute to its crosslinking capability, enhancing the mechanical properties of the resulting polymers. The low viscosity of TPGDA facilitates easy handling and incorporation into formulations.
Application
Tri(propylene glycol) diacrylate, mixture of isomers can be used:
- As a cross linker to synthesize resins for flexible micromaterials via projection microstereolithography (PμSL) screening formulations to fabricate microfluidic devices for cellular biosensors.
- As a dopant to prepare pure organic molecules with persistent luminescence at room temperature via intramolecular electronic coupling for forensic fingerprint detection.
- As a precursor to prepare high mechanical resilience double network hydrogel adhesives for wound healing patches.
signalword
Warning
hcodes
Hazard Classifications
Aquatic Chronic 2 - Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3
target_organs
Respiratory system
Clase de almacenamiento
10 - Combustible liquids
wgk
WGK 2
flash_point_f
307.4 °F - closed cup
flash_point_c
153 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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L A Nylander-French
The Annals of occupational hygiene, 44(8), 645-651 (2000-12-08)
Current methods for measuring dermal exposure to skin irritants and allergens, such as acrylates, have significant drawbacks for exposure assessment. A noninvasive sampling method has been developed and tested for measuring dermal exposure to a multifunctional acrylate employing a tape
J Surakka et al.
The Annals of occupational hygiene, 44(8), 635-644 (2000-12-08)
The use of ultraviolet radiation-curable coatings (UV-coatings) has increased rapidly in the parquet and furniture industry. Work with UV-coatings involves risk from skin exposure to chemically reactive, concentrated acrylates that are known skin contact irritants and sensitizers. Yet, the methods
Bor-Shiunn Lee et al.
Journal of endodontics, 34(5), 594-598 (2008-04-26)
We have developed a visible-light curable urethane-acrylate/tripropylene glycol diacrylate (UA/TPGDA) oligomer to serve as a root canal sealer and a zinc oxide/thermoplastic polyurethane (ZnO/TPU) composite to serve as a root canal obturation material. The purpose of this study was to
L A Nylander-French et al.
Toxicologic pathology, 26(4), 476-483 (1998-08-26)
The toxicity of the esters of acrylic acid are poorly understood even though significant human exposure occurs. To conduct rapid comparative short-term bioassays, we used the Tg.AC (v-Ha-ras) transgenic mouse model to determine the toxicity and potential carcinogenicity of tripropylene
R R Tice et al.
Environmental and molecular mutagenesis, 29(3), 240-249 (1997-01-01)
Acrylates may be polymerized to stable surface coatings (paints, lacquers, inks, etc.) by alkylation via the Michaelis-type addition reaction. Thus, acrylates have an inherent potential as electrophiles to be genotoxic, limited in their biological activity by their physicochemical properties. To
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