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105496-34-2

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105496-34-2 Usage

Description

Ovothiol C is a L-histidine derivative that features N,N-dimethyl-L-histidine with substitutions at positions N3 and C5 on the imidazole ring by methyl and mercapto groups, respectively. It is a unique compound with potential applications in various fields due to its distinct chemical properties.

Uses

Used in Pharmaceutical Industry:
Ovothiol C is used as a pharmaceutical compound for its potential therapeutic applications. The presence of the mercapto group provides it with antioxidant properties, which can be beneficial in the development of drugs targeting oxidative stress-related conditions.
Used in Chemical Research:
In the field of chemical research, ovothiol C can be utilized as a model compound to study the effects of specific substitutions on the properties and reactivity of histidine derivatives. This can contribute to the understanding of protein structure and function, as well as the design of new drugs and bioactive molecules.
Used in Antioxidant Formulations:
Due to its antioxidant properties, ovothiol C can be used as an additive in the development of antioxidant formulations for various industries, such as cosmetics, food, and nutraceuticals. Its ability to neutralize reactive oxygen species can help in preserving the quality and shelf life of products.
Used in Environmental Applications:
Ovothiol C's antioxidant capabilities can also be harnessed in environmental applications, such as in the remediation of contaminated sites or the development of eco-friendly materials. Its potential to mitigate oxidative stress in ecosystems could contribute to the overall health and sustainability of the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 105496-34-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,4,9 and 6 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 105496-34:
(8*1)+(7*0)+(6*5)+(5*4)+(4*9)+(3*6)+(2*3)+(1*4)=122
122 % 10 = 2
So 105496-34-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H15N3O2S/c1-11(2)7(9(13)14)4-6-8(15)10-5-12(6)3/h5,7,15H,4H2,1-3H3,(H,13,14)/t7-/m0/s1

105496-34-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name ovothiol C

1.2 Other means of identification

Product number -
Other names -

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:105496-34-2 SDS

105496-34-2Downstream Products

105496-34-2Related news

Heterocyclic thiols as antioxidants: Why ovothiol C (cas 105496-34-2) is a better antioxidant than ergothioneine07/14/2019

Spectral, acid-base, and redox properties of 4-mercaptoimidazoles were investigated by pulse radiolysis in aqueous solutions. Thiyl radicals of 1-methyl-5-ethyl-4-mercaptoimidazole (MEMI) have weak absorption band at 330 nm, ϵ = 300 ± 60 M−1 cm−1. Because the ionic strength variation from 0.01 ...detailed

105496-34-2Relevant articles and documents

Total Synthesis of Marine Mercaptohistidines: Ovothiols A, B, and C

Holler, Tod P.,Ruan, Fuqiang,Spaltenstein, Andreas,Hopkins, Paul B.

, p. 4570 - 4575 (2007/10/02)

Syntheses of ovothiols A and C in optically active form and ovothiols A and B in racemic form are reported.In all cases, synthesis of an S-protected mercaptoimidazole is followed by elaboration of an amino acid side chain.

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