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HomeProduct name listSulforhodamine B

Sulforhodamine B

Synonym(s):Acid Red 52;Kiton Red 620;Sulforhodamine B monosodium salt

  • CAS NO.:3520-42-1
  • Empirical Formula: C27H31N2NaO7S2
  • Molecular Weight: 582.66
  • MDL number: MFCD00010180
  • EINECS: 222-529-8
  • SAFETY DATA SHEET (SDS)
  • Update Date: 2024-10-31 20:01:59
Sulforhodamine B Structural

What is Sulforhodamine B?

Chemical properties

This substance is a deep red powder. It is easily soluble in water, forming a bluish-red solution with yellow fluorescence. When sodium hydroxide solution is added, it also appears bluish-red. Additionally, it is soluble in ethanol. In concentrated sulfuric acid, it turns orange-yellow and red after dilution.

The Uses of Sulforhodamine B

Sulforhodamine B Sodium Salt is a rhodamine dye widely used in nonpermanent tattoos. Studies show that Sulforhodamine B can be used as a potential new therapeutic agent for the treatment of the acute respiratory distress syndrome. Dyes and metabolites, Environmental Testing

The Uses of Sulforhodamine B

Sulforhodamine B sodium salt has been used:

  • for relative total cell mass quantification
  • to investigate the viscosity of coacervates
  • as a molecular rotor for microviscosity determination in aerosol droplets

What are the applications of Application

Sulforhodamine B (SRB) is known for use in SRB assay for the determination of in vitro cytotoxicity through staining and the observation of live cells, proliferation and drug screening.
It has been used in the SRB assay to evaluate the effect of mouthwashes on protein content in primary cultures of human fibroblasts.
It is also suitable as a microscopic tracer for the assessment of blood-brain barrier integrity by post mortem inspection of frozen sections. SRB is useful as a caries detector dye with subsequent inspection of histological material.

What are the applications of Application

Sulforhodamine B sodium salt is a fluorescent rhodamine dye, widely used in nonpermanent tattoos and potentially as a new therapeutic agent.

Definition

ChEBI: Sulforhodamine B is an organic sodium salt having 4-[3,6-bis(diethylamino)-2,7-dimethylxanthenium-9-yl]benzene-1,3-disulfonate as the counterion.

Preparation

4-Formylbenzene-1,3-disulfonic acid and 3-(Diethylamino)phenol condensation, the products with sulfuric acid dehydration, and ferric chloride oxidation, and finally into sodium salt.

General Description

Sulforhodamine B (SRB) is a bright-pink aminoxanthene dye. The sulforhodamine B (SRB) assay is extensively used for in vitro cytotoxicity screening. SRB binds to the protein constituents of the cells in a stoichiometric manner. Thus, the amount of dye extracted from stained cells is directly proportional to the cell mass. SRB can also be used for cell density determination.

Flammability and Explosibility

Not classified

Biochem/physiol Actions

Sulforhodamine B sodium salt is useful to measure cell biomass and also for cytotoxicity screening.

Properties and Applications

bright blue light pink. Dark red light brown powder. Soluble in water, in blue light red, with fluorescence, also soluble in alcohol. The strong sulfuric acid dyes is orange, diluted for red, with sodium hydroxide solution is blue light red. Mainly used for wool, silk and polyamide fiber dyeing, also can be used for wool and a variety of fabric dyeing, still can be in wool and silk fabric printing directly, also can used for leather dyeing.

Standard Light Fastness Soaping Persperation Fastness Oxygen bleaching Fastness to seawater
Fading Stain Fading Stain Fading Stain
ISO 3 3-4 3 4 1 2 3 2
AATCC 2-3 3 3 3 1 2 4 2-3

Properties of Sulforhodamine B

Density  1.472[at 20℃]
storage temp.  room temp
solubility  methanol: 1 mg/mL
form  powder
Colour Index  45100
color  Brown to Very Dark Purple
Water Solubility  95.3g/L at 20℃
BRN  3886008
EPA Substance Registry System C.I. Acid Red 52 (3520-42-1)

Safety information for Sulforhodamine B

Computed Descriptors for Sulforhodamine B

InChIKey XCRMYPBRGZRYEU-UHFFFAOYSA-N
SMILES S(C1C=C(S(O)(=O)=O)C=CC=1C1C2=CC=C(N(CC)CC)C=C2[O+]=C2C=C(N(CC)CC)C=CC=12)([O-])(=O)=O.[NaH]

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