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340855

Sigma-Aldrich

Glutaraldéhyde solution

50 wt. % in H2O

Synonyme(s) :

Dialdéhyde glutarique solution, Pentane-1,5-dial

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About This Item

Formule linéaire :
OHC(CH2)3CHO
Numéro CAS:
Poids moléculaire :
100.12
Numéro Beilstein :
605390
Numéro MDL:
Code UNSPSC :
12352114
ID de substance PubChem :
Nomenclature NACRES :
NA.21

Densité de vapeur

1.05 (vs air)

Niveau de qualité

Pression de vapeur

15 mmHg ( 20 °C)

Forme

liquid

Concentration

50 wt. % in H2O

Technique(s)

electron microscopy: suitable
immunoblotting: suitable
immunohistochemistry: suitable

Couleur

colorless

Indice de réfraction

n20/D 1.42

Pf

-21  °C ((-6 °F))

Solubilité

water: soluble

Densité

1.106 g/mL at 25 °C

Adéquation

suitable for microfluidics/nanofluidics

Application(s)

cell analysis
genomic analysis
life science and biopharma
sample preparation

Chaîne SMILES 

[H]C(CCCC([H])=O)=O

InChI

1S/C5H8O2/c6-4-2-1-3-5-7/h4-5H,1-3H2

Clé InChI

SXRSQZLOMIGNAQ-UHFFFAOYSA-N

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Description générale

Glutaraldehyde (Glutaric dialdehyde, Pentane-1,5-dial) is an aliphatic dialdehyde that can be employed as an effective biochemical reagent for various purposes such as a protein crosslinker, enzyme immobilization in microscopy, histochemistry, and cytochemistry. It serves as an amine-reactive homobifunctional crosslinker and a cell fixative before SDS-PAGE, staining, or electron microscopy, making it suitable for a wide range of morphological studies.

Glutaraldehyde is capable of efficiently crosslinking amine and hydrazine derivatives to proteins and other amine-containing polymers. Notably, in certain reactions, biotin hydrazides have been directly coupled to nucleic acids using glutaraldehyde, presenting a potential utility in conjugating fluorescent hydrazides and hydroxylamines to DNA. In histology studies, Glutaraldehyde is also employed to preserve tissue sections and prepare them for closer examination.

Application

Cross-linking agent for gelatin, poly(vinyl alcohol), and polyheptapeptides.
Glutaraldehyde may be used in the following studies:
  • To compose the fixative solution (Glutaraldehyde + Paraformaldehyde + NaPO4) for use in high-resolution light microscopy and electron microscopy studies.
  • To study the conjugation of goat anti-horseradish peroxidase with alkaline phosphatase by a reported method.
  • To compose the primary fixative, which is employed to protect the deterioration of cytoplasmic features of yeast cells during permanganate fixation.

Caractéristiques et avantages

  • Versatile and adaptable for wide variety of research applications
  • Ready-made solution reduces the need for preparation time

Autres remarques

For additional information on our range of Biochemicals, please complete this form.
To gain a comprehensive understanding of our extensive range of Monosaccharides for your research, we encourage you to visit our Carbohydrates Category page.

Mention d'avertissement

Danger

Classification des risques

Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 2 - Eye Dam. 1 - Resp. Sens. 1 - Skin Corr. 1B - Skin Sens. 1 - STOT SE 3

Organes cibles

Respiratory system

Risques supp

Code de la classe de stockage

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

Classe de danger pour l'eau (WGK)

WGK 3


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Les clients ont également consulté

Minutes Int. Symp. Microencapsulation, 9th, 191-191 (1993)
Polymer Journal (1993)
Biomimetics, 1, 219-219 (1992)
Chem. Abstr., 121, 52250t-52250t (1994)
Preservation of fine structures in yeast by fixation in a dimethyl sulfoxide-acrolein-glutaraldehyde solution.
D W Schwab et al.
Stain technology, 45(4), 143-147 (1970-07-01)

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