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473340

Sigma-Aldrich

1,3,5-Triacryloylhexahydro-1,3,5-triazin

98%

Synonym(e):

1,3,5-Triacryloyl-s -triazine, 1,3,5-Triacryloylhexahydro-s -triazine, 1,3,5-Triacryloylhexahydrotriazine, Tri(N -acryloyl)hexahydrotriazine, Triacrylformal

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About This Item

Empirische Formel (Hill-System):
C12H15N3O3
CAS-Nummer:
959-52-4
Molekulargewicht:
249.27
EG-Nummer:
213-501-6
MDL-Nummer:
MFCD00035738
UNSPSC-Code:
12162002
PubChem Substanz-ID:
24870897
NACRES:
NA.23

Qualitätsniveau

100

Assay

98%

mp (Schmelzpunkt)

156 °C (dec.) (lit.)

SMILES String

C=CC(=O)N1CN(CN(C1)C(=O)C=C)C(=O)C=C

InChI

1S/C12H15N3O3/c1-4-10(16)13-7-14(11(17)5-2)9-15(8-13)12(18)6-3/h4-6H,1-3,7-9H2

InChIKey

FYBFGAFWCBMEDG-UHFFFAOYSA-N

Verwandte Kategorien

Signalwort

Danger

Gefahreneinstufungen

Acute Tox. 2 Dermal - Acute Tox. 3 Inhalation - Eye Dam. 1 - Resp. Sens. 1 - Skin Corr. 1B - Skin Sens. 1

Lagerklassenschlüssel

6.1A - Combustible, acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges, type P3 (EN 143) respirator cartridges

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I Sereĭkaĭte et al.
Bioorganicheskaia khimiia, 29(3), 254-257 (2003-07-09)
The kinetics of the nucleophilic addition reactions of divinyl sulfone to amino groups of glycine and model proteins was studied in aqueous solution at 30 degrees C. The rate constants for glycine, bovine serum albumin, and alpha 1-casein were (4.84
G Patras et al.
Electrophoresis, 21(17), 3843-3850 (2001-03-29)
The properties of polyacrylamide hydrogels synthesized with a novel hexafunctional (three double bonds) cross-linker, hexahydro-1,3,5-triacryloyl-s-triazine (1a), was evaluated and compared to the currently used tetrafunctional (two double bonds) cross-linker N,N-methylenebisacrylamide (Bis). A variety of characterization techniques that require very little
R S Slesinski et al.
Toxicology, 40(2), 145-163 (1986-08-01)
TAHT (1,3,5-triacryloylhexahydro-s-triazine), a reactive chemical coupling agent, was highly toxic following a single peroral dose of an aqueous suspension (10% w/v) to Wistar rats, or following application of TAHT in dichloromethane (DCM) solution (10% w/v) to covered skin of New
G Dienys et al.
Bioconjugate chemistry, 9(6), 744-748 (1998-11-17)
Six difunctional and trifunctional derivatives of acrylamide were synthesized and investigated as potential protein lysine residue cross-linking agents. 1,3,5-Triacryloyl-hexahydro-s-triazine (TAT) was considered the best. The rate constants for the reactions of TAT with model nucleophiles in water solution at 25
Jolanta Sereikaite et al.
Acta biochimica Polonica, 53(1), 87-92 (2006-03-28)
The ability of Congo red to form complexes with alpha-proteins, human growth hormone and human interferon-alpha2b, was found by absorption difference spectroscopy. A human growth hormone-Congo red complex was isolated by gel-permeation chromatography, and its visible absorption spectrum was registered
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