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Merck
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資料

473340

Sigma-Aldrich

1,3,5-トリアクリロイルヘキサヒドロ-1,3,5-トリアジン

98%

別名:

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

実験式（ヒル表記法）:
C12H15N3O3
CAS番号:
959-52-4
分子量:
249.27
EC Number:
213-501-6
MDL番号:
MFCD00035738
UNSPSCコード:
12162002
PubChem Substance ID:
24870897
NACRES:
NA.23

品質水準

100

アッセイ

98%

mp

156 °C (dec.) (lit.)

SMILES記法

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

関連するカテゴリー

ピクトグラム

CorrosionSkull and crossbonesHealth hazard
GHS05,GHS06,GHS08

シグナルワード

Danger

危険有害性の分類

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

保管分類コード

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

WGK

WGK 3

引火点(°F)

Not applicable

引火点(℃)

Not applicable

個人用保護具 (PPE)

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

試験成績書（COA）

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以前この製品を購入いただいたことがある場合

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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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