Welcome to LookChem.com Sign In|Join Free

CAS

  • or

19901-15-6

Post Buying Request

19901-15-6 Suppliers

Recommended suppliersmore

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

19901-15-6 Usage

Uses

ACETALDEHYDE-2,2,2-D3 is used as a derivatizing agent in the measurement of endogenous epinephrine and norepinephrine in human plasma. It is also used to label the amine groups on biogenic monoamine neur otransmitters for simultaneous panel determination.

Check Digit Verification of cas no

The CAS Registry Mumber 19901-15-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,9,0 and 1 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 19901-15:
(7*1)+(6*9)+(5*9)+(4*0)+(3*1)+(2*1)+(1*5)=116
116 % 10 = 6
So 19901-15-6 is a valid CAS Registry Number.
InChI:InChI=1/C2H4O/c1-2-3/h2H,1H3/i1D3

19901-15-6SDS

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 2,2,2-trideuterioacetaldehyde

1.2 Other means of identification

Product number -
Other names 1,1,1-trideuterioacetaldehyde

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:19901-15-6 SDS

19901-15-6Downstream Products

19901-15-6Relevant articles and documents

Heptakis-6-amino-6-deoxy-β-cyclodextrin as a catalyst for H/D exchange

Binder, Wolfgang H.,Menger, Fredric M.

, p. 8963 - 8966 (1996)

Heptakis-6-amino-6-deoxy-β-cyclodextrin 2 at pD = 6.50, 20°C catalyzes CH/CD exchange in malonic acid, pyruvic acid and acetaldehyde. Accelerations as large as 3800 were observed. Copyright (C) 1996 Elsevier Science Ltd.

Selective oxidation of ethanol to acetaldehyde on gold

Gong, Jinlong,Mullins, C. Buddie

, p. 16458 - 16459 (2008)

We present results from an investigation of the oxidative conversion of ethanol into acetaldehyde on Au(111) employing temperature-programmed desorption (TPD) and molecular beam reactive scattering (MBRS). Results from isotopic experiments show that ethan

Capwell

, p. 1436 (1968)

Fermi resonance structure in the CH vibrational overtones of CD3CHO

Amrein, A.,Hollenstein, H.,Quack, M.,Zenobi, R.,Segall, J.,Zare, R. N.

, p. 3944 - 3951 (2007/10/02)

Gas-phase fundamental and CH and CO overtone spectra (700-17 500 cm-1) of 2,2,2- trideuteroacetaldehyde were recorded using FTIR and laser photoacoustic techniques.The Fermi resonance structure in the overtone spectra of the coupled CH stretching and in-plane CH bending vibrations is analy zed with a tridiagonal Hamiltonian yielding a large effective coupling constant, =93 cm-1, corresponding to subpicosecond redistribution times.No coupling between the out- of plane CH bending mode and the Fermi resonance system is apparent.This study presents the first detailed analysis of the anharmonic couplings in the CH chromophore at an sp2 carbon atom.The in- plane CH bending vibration couples in a manner similar to the CH ( sp3 ) bending vibrations, whereas the out-of plane bending vibration is decoupled, similar to the CH(sp) bending vibrations.

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 19901-15-6