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473340

Sigma-Aldrich

1,3,5-Triacryloylhexahydro-1,3,5-triazine

98%

Sinónimos:

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

Fórmula empírica (notación de Hill):
C12H15N3O3
Número de CAS:
959-52-4
Peso molecular:
249.27
EC Number:
213-501-6
MDL number:
MFCD00035738
UNSPSC Code:
12162002
PubChem Substance ID:
24870897
NACRES:
NA.23

Quality Level

100

assay

98%

mp

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

InChI key

FYBFGAFWCBMEDG-UHFFFAOYSA-N

signalword

Danger

Hazard Classifications

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

Storage Class

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

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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

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Certificados de análisis (COA)

Lot/Batch Number
MKCW0708
MKCV1290
MKCV2385
MKCS5051
MKCP6497

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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, 11(5), 646-651 (2000-09-20)
Zn(2+) and Co(2+) ions are known to promote human growth hormone reversible dimerization. In these studies, dimerization was also shown to be initiated by nine other metal ions: Cd(2+), Hg(2+), Cu(2+), Ag+, Au(3+), Au+, Pd(2+), Ni(2+), and Pt(4+). In some
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
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
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
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