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Merck
CN

473340

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

98%

Synonym(s):

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

Empirical Formula (Hill Notation):
C12H15N3O3
CAS Number:
959-52-4
Molecular Weight:
249.27
NACRES:
NA.23
PubChem Substance ID:
24870897
UNSPSC Code:
12162002
EC Number:
213-501-6
MDL number:
MFCD00035738

Key Documents

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InChI key

FYBFGAFWCBMEDG-UHFFFAOYSA-N

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

SMILES string

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

assay

98%

mp

156 °C (dec.) (lit.)

Quality Level

100

Related Categories

signalword

Danger

Storage Class

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

wgk

WGK 3

ppe

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

pictograms

Skull and crossbones
GHS06

Hazard Classifications

Acute Tox. 2 Dermal - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Sens. 1B

flash_point_f

No data available

flash_point_c

No data available

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Certificates of Analysis (COA)

Lot/Batch Number
MKCZ9507
MKCW0708
MKCV1290
MKCV2385
MKCS5051

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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
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
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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