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02191

Sigma-Aldrich

Di-hidrazida de ácido adípico

purum, ≥97.0% (NT)

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About This Item

Fórmula linear:
NH2NHCO(CH2)4CONHNH2
Número CAS:
1071-93-8
Peso molecular:
174.20
Beilstein:
973863
Número CE:
213-999-5
Número MDL:
MFCD00007614
Código UNSPSC:
12352200
ID de substância PubChem:
329747401

grau

purum

Ensaio

≥97.0% (NT)

pf

180-182 °C (lit.)
180-182 °C

cadeia de caracteres SMILES

NNC(=O)CCCCC(=O)NN

InChI

1S/C6H14N4O2/c7-9-5(11)3-1-2-4-6(12)10-8/h1-4,7-8H2,(H,9,11)(H,10,12)

chave InChI

IBVAQQYNSHJXBV-UHFFFAOYSA-N

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Aplicação

Adipic acid dihydrazide can be used to study chemical synthesis, organic building blocks, carbonyl compounds and hydrazides. Adipic acid dihydrazide has been used in a study to show that diphtheria toxoid can be successfully employed as a carrier protein for conjugation with Salmonella O-specific polysaccharides and play an important role in facilitating adequate immune response in typhoid fever vaccines. Adipic acid dihydrazide has also been used in a study to assess the activity of the derivatives of glycoside steviolbioside from the plant Stevia rebaudiana.

Outras notas

Bifunctional linker employed for the immobilization of carbohydrates, e.g. to MMAC resins (methyl vinyl ether, maleic anhydride co-polymer)[1][2]

substituído por

Nº do produto
Descrição
Preços

Pictogramas

Environment
GHS09

Frases de perigo

H411

Declarações de precaução

P273 - P391 - P501

Classificações de perigo

Aquatic Chronic 2

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

302.0 °F - closed cup

Ponto de fulgor (°C)

150 °C - closed cup

Equipamento de proteção individual

Eyeshields, Gloves, type N95 (US)

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Certificados de análise (COA)

Lot/Batch Number

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A Satoh et al.
Analytical biochemistry, 260(1), 96-102 (1998-07-02)
We have previously reported a method to immobilize protein ligands on microtiter plates coated with methyl vinyl ether-maleic anhydride copolymer (MMAC) [Isosaki, K., et al. (1992) J. Chromatogr. 597, 123-128]. In this study, we improved the MMAC method to efficiently
A Satoh et al.
Analytical biochemistry, 275(2), 231-235 (1999-12-20)
The immobilization of carbohydrates for solid-phase assays, including enzyme-linked immunosorbent assay (ELISA), is difficult because they are hydrophilic. We developed four new methods for the immobilization of oligosaccharides. ELISA plates were first coated with methyl vinyl ether-maleic anhydride copolymer (MMAC)
Wen-Yu Su et al.
Journal of biomaterials science. Polymer edition, 22(13), 1777-1797 (2010-09-17)
Vitrectomy is a common procedure for treating ocular-related diseases. The surgery involves removing the vitreous humor from the center of the eye, and vitreous substitutes are needed to replace the vitreous humor after vitrectomy. In the present study, we developed
O Joshi et al.
Colloids and surfaces. B, Biointerfaces, 50(1), 26-35 (2006-05-09)
Heparin was modified with adipic dihydrazide and covalently linked to surface-activated silica wafers. X-ray photoelectron spectroscopy was used at each stage of derivatization and showed that successful immobilization had taken place. Surfaces were imaged with atomic force microscopy to determine
Tulsidas G Shrivastav
Journal of immunoassay & immunochemistry, 24(3), 301-309 (2003-09-05)
Preparation of horseradish peroxidase (HRP) hydrazide that is HRP linked to adipic acid dihydrazide (HRP-ADH) and its use in enzyme immunoassay (EIA) is described. In this new strategy, horseradish peroxidase was conjugated to adipic acid dihydrazide using a carbodiimide coupling
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