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Merck

340855

Glutaraldehyde solution

50 wt. % in H2O

Sinónimos:

Glutaric dialdehyde solution, Pentane-1,5-dial

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About This Item

Fórmula lineal:
OHC(CH2)3CHO
Número CAS:
Peso molecular:
100.12
UNSPSC Code:
12352114
NACRES:
NA.21
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
605390

Nombre del producto

Glutaraldehyde solution, 50 wt. % in H2O

InChI

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

SMILES string

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

InChI key

SXRSQZLOMIGNAQ-UHFFFAOYSA-N

vapor density

1.05 (vs air)

vapor pressure

15 mmHg ( 20 °C)

form

liquid

concentration

50 wt. % in H2O

technique(s)

electron microscopy: suitable
immunoblotting: suitable
immunohistochemistry: suitable

color

colorless

refractive index

n20/D 1.42

mp

-21  °C ((-6 °F))

solubility

water: soluble

density

1.106 g/mL at 25 °C

suitability

suitable for microfluidics/nanofluidics

application(s)

cell analysis
genomic analysis
life science and biopharma
sample preparation

Quality Level

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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.

Features and Benefits

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

General description

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.

Other Notes

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.

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Danger

Hazard Classifications

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

target_organs

Respiratory system

supp_hazards

Clase de almacenamiento

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

wgk

WGK 3


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Visite la Librería de documentos

Minutes Int. Symp. Microencapsulation, 9th, 191-191 (1993)
Biomimetics, 1, 219-219 (1992)
Chem. Abstr., 121, 52250t-52250t (1994)
Polymer Journal (1993)
Plastic Embedding and Sectioning of Plant Tissues.
Liu T.
Bio-protocol, 2(23) (2012)

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