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15905-32-5

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15905-32-5 Usage

Chemical Properties

orange-red fine powder

Uses

Different sources of media describe the Uses of 15905-32-5 differently. You can refer to the following data:
1. Indicator in analytical chemistry.
2. Erythrosin B is used as a red coloring in some foods such as cherries and fish. It is used as printing ink, dental plaque disclosing agent and biological stain. It finds application as a radiopaque medium and sensitizer for orthochromatic photographic films. It is utilized as a cake-decorating gel. In addition to this, it is used in sweets such as candies and popsicles.
3. Erythrosin B has been used as a dye in fluorescence lifetime imaging.

Preparation

Fluorescein (C.I.Acid Yellow 73, C.L 45350) in aqueous solution or Tetraiodide in ethanol, and made ??the free acid form.

Biochem/physiol Actions

Erythrosin B, also called as eosin B, is a xanthene dye. It belongs to the family of fluorescein dyes. It plays a major role in inhibiting dopamine uptake and high affinity 3H-ouabain binding and ion transport in synaptosomes from rat caudate nucleus.

Properties and Applications

blue light red. Soluble in water for cherry red, no fluorescence. In concentrated sulfuric acid for brown light yellow, dilution after brown light yellow precipitation. Dye aqueous solution to join sodium hydroxide have soluble precipitation. Used in cosmetics coloring. Standard Light Fastness Heat-resistant(℃) water Sodium Carbonate(5%) Hydrochloric acid(5%) Melting point Stable ISO Poor Insoluble

Standard

Light Fastness

Melting point

Stable

ISO

Poor

Check Digit Verification of cas no

The CAS Registry Mumber 15905-32-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,9,0 and 5 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 15905-32:
(7*1)+(6*5)+(5*9)+(4*0)+(3*5)+(2*3)+(1*2)=105
105 % 10 = 5
So 15905-32-5 is a valid CAS Registry Number.

15905-32-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name Erythrosin B

1.2 Other means of identification

Product number -
Other names Solvent Red 140

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Food additives
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:15905-32-5 SDS

15905-32-5Synthetic route

fluorescein
2321-07-5

fluorescein

A

2',4',5'-triiodofluorescein
56254-06-9

2',4',5'-triiodofluorescein

B

erythrosine B
15905-32-5

erythrosine B

Conditions
ConditionsYield
With Oxone; sodium iodide at 200℃; for 12h;A 70%
B 30%
ethanol
64-17-5

ethanol

fluorescein
2321-07-5

fluorescein

erythrosine B
15905-32-5

erythrosine B

Conditions
ConditionsYield
With pyridine; iodine; silver nitrate
fluorescein
2321-07-5

fluorescein

erythrosine B
15905-32-5

erythrosine B

Conditions
ConditionsYield
With iodine Behandeln mit Eisessig;
With sodium hydroxide; iodine; acetic acid
With dihydrogen peroxide; sodium iodide In ethanol at 20℃; for 5h; Autoclave; Large scale;
Erythrosin

Erythrosin

erythrosine B
15905-32-5

erythrosine B

Conditions
ConditionsYield
With oxygen Irradiation; photo-bleaching in some polymer-films: permeability of O2, glass-transition-temp., rel. index of polarity, quantum yield of bleaching, influence of O2;
acetyl chloride
75-36-5

acetyl chloride

erythrosine B
15905-32-5

erythrosine B

erythrosin B diacetate
77084-69-6

erythrosin B diacetate

Conditions
ConditionsYield
With pyridine; dmap In dichloromethane for 1h;32%
1-hydroxy-pyrrolidine-2,5-dione
6066-82-6

1-hydroxy-pyrrolidine-2,5-dione

erythrosine B
15905-32-5

erythrosine B

erythrosin n-hydroxysulfosuccinimide

erythrosin n-hydroxysulfosuccinimide

Conditions
ConditionsYield
dicyclohexyl-carbodiimide In DMF (N,N-dimethyl-formamide) at 4 - 20℃;
polycaprolactone diol terminated with 3,5-bis(acetylamino)-2,4,6-triiodobenzoic acid

polycaprolactone diol terminated with 3,5-bis(acetylamino)-2,4,6-triiodobenzoic acid

erythrosine B
15905-32-5

erythrosine B

trifunctional lactate polymer with erythrosin

trifunctional lactate polymer with erythrosin

Conditions
ConditionsYield
dicyclohexyl-carbodiimide In benzene at 0℃; for 72h;
polyethylene glycol 1000

polyethylene glycol 1000

erythrosine B
15905-32-5

erythrosine B

polyethylene glycol; erythrosin-terminated

polyethylene glycol; erythrosin-terminated

Conditions
ConditionsYield
With dmap; dicyclohexyl-carbodiimide In DMF (N,N-dimethyl-formamide) at 0℃; for 16h;
erythrosine B
15905-32-5

erythrosine B

2',4',5',7'-tetraiodofluorescein disodium salt
16423-68-0, 63467-67-4

2',4',5',7'-tetraiodofluorescein disodium salt

Conditions
ConditionsYield
With sodium hydroxide In water at 20℃; for 4.5h; Autoclave; Large scale;7.9 kg
erythrosine B
15905-32-5

erythrosine B

sodium thiomethoxide
5188-07-8

sodium thiomethoxide

C21H13I3O5S

C21H13I3O5S

Conditions
ConditionsYield
Stage #1: erythrosine B; sodium thiomethoxide With acetic anhydride
Stage #2: With tetrakis(triphenylphosphine) palladium(0) Further stages;

15905-32-5Relevant articles and documents

Technique for preparing erythrosin B

-

Paragraph 0041; 0042; 0043; 0047, (2017/04/19)

The invention discloses a technique for preparing erythrosin B. The technique comprises the steps of 1, making fluorescein which serves as the start material react with iodate to generate erythrosine under the action of a solvent and a catalyst; 2, making the erythrosine prepared in step 1 react with alkali to generate the erythrosine B under the action of a solvent. The technique has the advantages that operation is easy, cost is low, yield is high, pollution is light, and iodine utilization rate is high. The technique is suitable for industrial production and is suitable for production of most relevant enterprises.

Assay for mycobacterium avium/intracellulare nucleic acid

-

, (2010/12/26)

Disclosed is a method for determining the presence of Mycobacterium avium complex nucleic acids in a biological sample. In particular, the mig gene of M. avium and the DT1 gene of M. intracellulare are detected, preferably following amplification. In addition, the method distinguishes between species of M. avium and M. intracellulare. Also described are oligonucleotides that can be used as primers to amplify target genes such as mig and DT1 genes and as probes as well as kits containing the oligonucleotides.

PROCESS FOR SYNTHESIZING HALOGENATED DERIVATIVES OF FLUORESCEIN FOR USE IN THE PRODUCTION OF NON-VOLATILE MEMORY DEVICES

-

Page/Page column 7, (2008/06/13)

A process performs solid phase synthesis of halogenated derivatives of fluorescein, and includes reacting fluorescein with a halide MX, wherein M is an alkali metal and X is a halogen, and Oxone? (2 KHSO5.KHSO4.K2SO4), at a temperature higher than or equal to 150° C. A structure uses a halogenated derivative of fluorescein selected from the group consisting of 2′,4′,5′-trichlorofluorescein, 2′,4′,5′,7′-tetrachlorofluorescein, 4′,5′-diiodofluorescein diacetate and 2′,4′,5′-triiodofluorescein as electro-bistable material in a non-volatile memory device.

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