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Merck
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Key Documents

156868

Sigma-Aldrich

(+)-N,N′-Diallyltartramide

≥99%

Sinônimo(s):

N,N′-Diallyl L-tartardiamide, N,N′-Diallyltartramide, DATD

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About This Item

Fórmula linear:
[CH(OH)CONHCH2CH=CH2]2
Número CAS:
Peso molecular:
228.25
Beilstein:
1712934
Número CE:
Número MDL:
Código UNSPSC:
12352002
ID de substância PubChem:
NACRES:
NA.22

Nível de qualidade

Ensaio

≥99%

atividade óptica

[α]20/D +108°, c = 2.4 in H2O

pf

186-188 °C (lit.)

cadeia de caracteres SMILES

O[C@H]([C@@H](O)C(=O)NCC=C)C(=O)NCC=C

InChI

1S/C10H16N2O4/c1-3-5-11-9(15)7(13)8(14)10(16)12-6-4-2/h3-4,7-8,13-14H,1-2,5-6H2,(H,11,15)(H,12,16)/t7-,8-/m1/s1

chave InChI

ZRKLEAHGBNDKHM-HTQZYQBOSA-N

Descrição geral

(+)-N,N′-Diallyltartramide can be used as a cross-linking agent during the preparation of hydrogels.

Aplicação

(+)-N,N′-Diallyltartramide can be used as a crosslinking agent:
  • In the polymerization of soluble polyacrylamide gels for electrophoresis applications.
  • In the preparation of hydrogel containing cellulose, which is used as a component of an actuator capable of controlled soil irrigation.
  • In the synthesis of dendronized polymers, which are used to prepare hydrogels containing ciprofloxacin for controlled drug release.

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

dust mask type N95 (US), Eyeshields, Gloves


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A simplified approach to synthesize nonparticulate (continuous or monolithic) beds with embedded vancomycin chiral selectors for capillary electrochromatography is proposed. In the present approach, N,N'-diallyltartardiamide monomer with diol functionality is used, which can be readily converted to aldehyde groups via

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