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UROPORPHYRIN I ETHYL ESTER is a synthetic compound derived from porphyrin, an organic compound that naturally occurs in various biological systems. It is characterized by its fluorescent properties, which make it a valuable tool in medical research, particularly for imaging and tumor detection. UROPORPHYRIN I ETHYL ESTER's ability to bind with certain biological molecules also facilitates its use in studying cellular processes and developing diagnostic tools. With its unique characteristics, UROPORPHYRIN I ETHYL ESTER holds potential applications across various fields, including medicine, biochemistry, and materials science.

54090-85-6

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54090-85-6 Usage

Uses

Used in Medical Research:
UROPORPHYRIN I ETHYL ESTER is used as a fluorescent marker for imaging and tumor detection due to its ability to bind with biological molecules and emit fluorescence.
Used in Biochemistry:
UROPORPHYRIN I ETHYL ESTER is used as a research tool for studying cellular processes, as its binding properties allow for the tracking and analysis of specific molecules within biological systems.
Used in Materials Science:
UROPORPHYRIN I ETHYL ESTER is used in the development of diagnostic tools and materials with potential applications in various industries, such as pharmaceuticals and biotechnology, due to its unique fluorescent properties and binding capabilities.

Check Digit Verification of cas no

The CAS Registry Mumber 54090-85-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,0,9 and 0 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 54090-85:
(7*5)+(6*4)+(5*0)+(4*9)+(3*0)+(2*8)+(1*5)=116
116 % 10 = 6
So 54090-85-6 is a valid CAS Registry Number.
InChI:InChI=1/C56H70N4O16/c1-9-69-49(61)21-17-33-37(25-53(65)73-13-5)45-30-42-35(19-23-51(63)71-11-3)39(27-55(67)75-15-7)47(59-42)32-44-36(20-24-52(64)72-12-4)40(28-56(68)76-16-8)48(60-44)31-43-34(18-22-50(62)70-10-2)38(26-54(66)74-14-6)46(58-43)29-41(33)57-45/h29-32,57,60H,9-28H2,1-8H3/b41-29-,42-30-,43-31-,44-32-,45-30-,46-29-,47-32-,48-31-

54090-85-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[7,12,17-tris(carboxymethyl)-3,8,13,18-tetrakis(3-ethoxy-3-oxopropyl)-21,22-dihydroporphyrin-2-yl]acetic acid

1.2 Other means of identification

Product number -
Other names 21H,23H-Porphine-2,7,12,17-tetrapropanoic acid,3,8,13,18-tetrakis(2-ethoxy-2-oxoethyl)-,tetraethyl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
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:54090-85-6 SDS

54090-85-6Downstream Products

54090-85-6Relevant academic research and scientific papers

Non-enzymic tetramisation of ethyl 3-(4-ethoxycarbonylmethyl-1H-pyrrol-3-yl)propionate with formaldehyde follows a similar course to the non-enzymic tetramisation of porphobilinogen

Cheung, Kwai-Ming,Shoolingin-Jordan, Peter M.

, p. 5973 - 5976 (2007/10/03)

The octaethyl esters of uroporphyrins were formed directly from ethyl 3-(4-ethoxy-carbonylmethyl-1H-pyrrol-3-yl)propionate and formalin in a yield of ca. 30% with the isomers I, II, III and IV being formed in the ratio 1:1:4:2. Under anaerobic conditions, the colourless uroporphyrinogen esters were formed in a similar ratio. These observations parallel the non-enzymic formation of uroporphyrinogens from the naturally occurring tetrapyrrole precursor, porphobilinogen, highlighting the similarity in both tetramisation and isomerisation reactions.

Molar absorption coefficients of porphyrin esters in chloroform determined by copper titration

With,Pedersen

, p. 425 - 429 (2007/10/09)

Chromatographically pure porphyrin esters free from metalloporphyrins were titrated with Cu2+ to determine the molar amount of porphyrin present. The end point of the titration was defined by a t.l.c. method detecting traces of metal free porphyrin ester in admixture to its copper complex. From spectrometic measurement at the Soret maximum and the molar amounts found by the titration, ε(M) was calculated for proto-, copro-, penta-, hexa- and hepta- carboxylic and uro porphyrin permethyl esters. The values for uroporphyrin showed perfect agreement with those of previous workers, whereas those for coproporphyrin were about 5% lower and those for protoporphyrin more than 20% lower. The implications of the findings are discussed. Determinations of ε(M) of some higher esters (ethyl to pentyl) and some partial methyl esters with one carboxyl group free are also presented.

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