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156868

Sigma-Aldrich

(+)-N,N′-Diallyltartramide

≥99%

Sinonimo/i:

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

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About This Item

Formula condensata:
[CH(OH)CONHCH2CH=CH2]2
Numero CAS:
58477-85-3
Peso molecolare:
228.25
Beilstein:
1712934
Numero CE:
261-277-3
Numero MDL:
MFCD00008640
Codice UNSPSC:
12352002
ID PubChem:
24849641
NACRES:
NA.22

Saggio

≥99%

Attività ottica

[α]20/D +108°, c = 2.4 in H2O

Punto di fusione

186-188 °C (lit.)

Stringa SMILE

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
ZRKLEAHGBNDKHM-HTQZYQBOSA-N

Categorie correlate

Descrizione generale

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

Applicazioni

(+)-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.

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves

Certificati d'analisi (COA)

Cerca il Certificati d'analisi (COA) digitando il numero di lotto/batch corrispondente. I numeri di lotto o di batch sono stampati sull'etichetta dei prodotti dopo la parola ‘Lotto’ o ‘Batch’.

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Journal of Chromatography A, 638, 165-165 (1993)
Ashish Khaparde et al.
Journal of pharmaceutical and biomedical analysis, 181, 113099-113099 (2020-01-25)
A generic multi-component approach was designed to perform simultaneous in situ polymerization and ligand immobilization to develop affinity porous polymer based chromatography resin in a facile mode. This strategy exploits the regioselective ring opening reaction between epoxy group of monomer
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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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