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50481-03-3

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50481-03-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 50481-03-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,4,8 and 1 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 50481-03:
(7*5)+(6*0)+(5*4)+(4*8)+(3*1)+(2*0)+(1*3)=93
93 % 10 = 3
So 50481-03-3 is a valid CAS Registry Number.

50481-03-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name (L-2)-tetra-n-butylammonium diiodoaurate(I)

1.2 Other means of identification

Product number -
Other names TETRABUTYLAMMONIUM DIIODOAURATE

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:50481-03-3 SDS

50481-03-3Relevant articles and documents

Unexpected complexity in the electro-oxidation of iodide on gold in the ionic liquid 1-ethyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imide

Bentley, Cameron L.,Bond, Alan M.,Hollenkamp, Anthony F.,Mahon, Peter J.,Zhang, Jie

, p. 11319 - 11325 (2013)

The electro-oxidation of iodide on a gold electrode in the room temperature ionic liquid 1-ethyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imide has been investigated using transient cyclic voltammetry, linear-sweep semi-integral voltammetry, an electrochemical quartz crystal microbalance technique, and coulometry/electrogravimetry. Two oxidation processes are observed, with an electron stoichiometry of 1:1, compared with the well-known 2:1 electron stoichiometry observed on other commonly used electrode materials, such as platinum, glassy carbon, and boron-doped diamond, under identical conditions. Detailed mechanistic information, obtained in situ using an electrochemical quartz crystal microbalance, reveals that this unusual observation can be attributed to the dissolution of the gold electrode in the presence of iodide. Coulometric/electrogravimetric analysis suggests that the oxidation state of the soluble gold species is +1 and that diiodoaurate, [AuI2]-, is the likely intermediate. A proportionally smaller amount of triiodide intermediate is also detected by means of UV-vis spectroscopy. On this basis, it is proposed that iodide oxidation on gold occurs via two parallel pathways: predominantly via a diiodoaurate intermediate 2I- + Au [AuI2]- + e- and [AuI 2]- I2 + Au + e- and to a lesser extent via a triiodide intermediate 3I- I3- + 2e- and I3- 3/2I2 + e-. This proposed mechanism was further supported by voltammetric investigations with an authentic sample of the anionic [AuI2]- complex.

Structural, Far-infrared and 31P Nuclear Magnetic Resonance Studies of Two-co-ordinate Complexes of Tris(2,4,6-trimethoxyphenyl)phosphine with Gold(I) Halides

Baker, Lisa-Jane,Bott, Raymond C.,Bowmaker, Graham A.,Healy, Peter C.,Skelton, Brian W.,et al.

, p. 1341 - 1348 (2007/10/02)

The complexes were prepared by reaction of tmpp with or (1-).The crystalline compounds are isomorphous with the corresponding complexes of Cu and Ag, with Au-P

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