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473340

Sigma-Aldrich

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

98%

Sinônimo(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

Fórmula empírica (Notação de Hill):
C12H15N3O3
Número CAS:
959-52-4
Peso molecular:
249.27
Número CE:
213-501-6
Número MDL:
MFCD00035738
Código UNSPSC:
12162002
ID de substância PubChem:
24870897
NACRES:
NA.23

Nível de qualidade

100

Ensaio

98%

pf

156 °C (dec.) (lit.)

cadeia de caracteres SMILES

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

chave InChI

FYBFGAFWCBMEDG-UHFFFAOYSA-N

Palavra indicadora

Danger

Frases de perigo

H310,H314,H317,H331,H334

Classificações de perigo

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

Código de classe de armazenamento

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

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

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

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Certificados de análise (COA)

Lot/Batch Number
MKCP6497
MKCP3078
MKCH5685
MKCD7180
MKCC1226

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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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