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L-Aspartic acid, N-[[4-[[4-(dimethylamino)phenyl]azo]phenyl]sulfonyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

87667-33-2

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87667-33-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87667-33-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,6,6 and 7 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 87667-33:
(7*8)+(6*7)+(5*6)+(4*6)+(3*7)+(2*3)+(1*3)=182
182 % 10 = 2
So 87667-33-2 is a valid CAS Registry Number.

87667-33-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-2-[[4-[[4-(dimethylamino)phenyl]diazenyl]phenyl]sulfonylamino]butanedioic acid

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:87667-33-2 SDS

87667-33-2Downstream Products

87667-33-2Relevant academic research and scientific papers

Combined Surface-Enhanced and Resonance-Raman Scattering from the Aspartic Acid Derivative of Methyl Orange on Colloidal Silver

Sliman, O.,Lepp, A.,Kerker, M.

, p. 5319 - 5325 (1983)

By selecting a chromophore, dabsyl (N-4-dimethylaminoazobenzene-4'-sulfonyl) aspartate (DABS-ASP), whose absorption spectrum overlaps with the surface-enhanced Raman scattering (SERS) excitation profile for colloidal silver sols, we have found it possible to study the triple combination of resonant Raman scattering (RRS) of the DABS-ASP in solution and both the combined RRS-SERS (SERRS) and the SERS of DABS-ASP adsorbed on the colloidal silver particles.The SERRS and SERS spectra were distinctly different from each other.The measured surface enhancements were in excess of 103.This is less than the values of the order of 105 measured earlier for citrate on these silver sols.Just as for citrate, the excitation profiles peaked at about 500 nm whereas the main absorption band was in the region of 400 nm, a disparity from our electrodynamic model for SERS.

Center-of-mass iso-energetic collision-induced decomposition in tandem triple quadrupole mass spectrometry

Rubino, Federico Maria

, (2020)

Two scan modes of the triple quadrupole tandem mass spectrometer, namely Collision Induced Dissociation Precursor Ion scan and Neutral Loss scan, allow selectively pinpointing, in a complex mixture, compounds that feature specific chemical groups, which yield characteristic fragment ions or are lost as distinctive neutral fragments. This feature of the triple quadrupole tandem mass spectrometer allows the non-target screening of mixtures for classes of components. The effective (center-of-mass) energy to achieve specific fragmentation depends on the inter-quadrupole voltage (laboratory-frame collision energy) and on the masses of the precursor molecular ion and of the collision gas, through a non-linear relationship. Thus, in a class of homologous compounds, precursor ions activated at the same laboratory-frame collision energy face different center-of-mass collision energy, and therefore the same fragmentation channel operates with different degrees of efficiency. This article reports a linear equation to calculate the laboratory-frame collision energy necessary to operate Collision-Induced Dissociation at the same center-of-mass energy on closely related compounds with different molecular mass. A routine triple quadrupole tandem mass spectrometer can operate this novel feature (iso-energetic collision-induced dissociation scan; i-CID) to analyze mixtures of endogenous metabolites by Precursor Ion and Neutral Loss scans. The latter experiment also entails the hitherto unprecedented synchronized scanning of all three quadrupoles of the triple quadrupole tandem mass spectrometer. To exemplify the application of this technique, this article shows two proof-of-principle approaches to the determination of biological mixtures, one by Precursor Ion analysis on alpha amino acid derivatized with a popular chromophore, and the other on modified nucleosides with a Neutral Fragment Loss scan.

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