Welcome to LookChem.com Sign In|Join Free

CAS

  • or

500-85-6

Post Buying Request

500-85-6 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

500-85-6 Usage

Uses

Indophenol is an artificial blue metachromatic dye. The formation of Indophenol can be used to determine ammonia and paracetamol by spectrophotometry.

Definition

ChEBI: A quinone imine obtained by formal condensation of one of the keto groups of benzoquinone with the amino group of 4-hydroxyaniline.

Check Digit Verification of cas no

The CAS Registry Mumber 500-85-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,0 and 0 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 500-85:
(5*5)+(4*0)+(3*0)+(2*8)+(1*5)=46
46 % 10 = 6
So 500-85-6 is a valid CAS Registry Number.
InChI:InChI=1/C12H9NO2/c14-11-5-1-9(2-6-11)13-10-3-7-12(15)8-4-10/h1-8,14H

500-85-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name indophenol

1.2 Other means of identification

Product number -
Other names 4-(4-hydroxyphenyl)iminocyclohexa-2,5-dien-1-one

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:500-85-6 SDS

500-85-6Relevant articles and documents

PURIFICATION AND PROPERTIES OF AN ESTERASE FROM CUCURBITA MAXIMA FRUIT TISSUE

Nourse, Amanda,Schabort, Johan C.,Dirr, Heini W.,Dubery, Ian A.

, p. 379 - 384 (1989)

An esterase from the fruit of Cucurbita maxima was purified to apparent homogeneity.The enzyme displays an Mr, of 36 000, a pI value of 4.9, a Stokes radius of 2.70 nm, diffusion coefficient of 9.25 x 1E-7 cm2/sec, possesses a homogeneous dimeric quaternary structure with a subunit Mr of 18 000.High esterolytic activity was observed with indophenyl acetate (1510 μmol/min/mg protein and p-nitrophenyl acetate (648 μmol/min/mg protein) while the enzyme displayed no carboxypeptidase, amidase, proteinase or aminopeptidase activities.Based on indophenyl acetate as substrate, the esterase has an optimum pH of 7.5 to 8.9 and a KM value.14 mM at pH 8.0.The esterolytic activity is strongly inhibited by mercaptide-forming and alkylating thiol reagents and by diisopropyl fluorophosphate and phenylmethylsulphonyl fluoride.Product inhibition by indophenyl was competitive (apparent Ki=90 μM) relative to indophenol acetate and parabolic.Acetate was without effect.Key Word Index - Cucurbita maxima; Cucurbitaceae; esterase.

Nitrite Reduction to Nitrous Oxide and Ammonia by TiO2 Electrons in a Colloid Solution via Consecutive One-Electron Transfer Reactions

Goldstein, Sara,Behar, David,Rajh, Tijana,Rabani, Joseph

, p. 2307 - 2312 (2016/05/19)

The mechanism of nitrite reduction by excess electrons on TiO2 nanoparticles (eTiO2-) was studied under anaerobic conditions. TiO2 was loaded with up to 75 electrons per particle, induced by γ-irradiation of acidic TiO2 colloid solutions containing 2-propanol. Time-resolved kinetics and material analysis were performed, mostly at 1.66 g L-1 TiO2. At relatively low nitrite concentrations (R = [eTiO2-]o/[nitrite]o > 1.5), eTiO2- decays via two consecutive processes; at higher concentrations, only one decay step is observed. The stoichiometric ratio Δ[eTiO2-]/[nitrite]o of the faster process is about 2. This process involves the one-electron reduction of nitrite, forming the nitrite radical (k1 = (2.0 ± 0.2) × 106 M-1 s-1), which further reacts with eTiO2- (k2) in competition with its dehydration to nitric oxide (NO) (k3). The ratios k2/k3 = (3.0 ± 0.5) × 103 M-1 and k2 > 1 × 106 M-1 s-1 were derived from kinetic simulations and product analysis. The major product of this process is NO. The slower stage of the kinetics involves the reduction of NO by eTiO2-, and the detailed mechanism of this process has been discussed in our earlier publication. The results reported in this study suggest that several intermediates, including NO and NH2OH, are adsorbed on the titanium nanoparticles and give rise to inverse dependency of the respective reaction rates on the TiO2 concentration. It is demonstrated that the reduction of nitrite by eTiO2- yields mainly N2O and NH3 via consecutive one-electron transfer reactions.

Polyfluoroalkoxy phosphonic and phosphinic acid derivatives: II. Reversible esterase inhibitors

Krutikova,Krutikov,Erkin

experimental part, p. 434 - 439 (2010/08/04)

Polyfluoroalkyl esters of phosphoric, alkylphosphonic and 1-hydroxypolyfluoroalkylphosphonic acids exhibited significant antiesterase activity against various esterases of animal and microbial origin. Moreover, with some compounds reversible inhibition of enzymes was observed due to the specific influence of hydrophobic fragments of the target products.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 500-85-6