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1-Hexanaminium, N,N,N-trihexyl-, methanesulfonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

105140-20-3

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105140-20-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 105140-20-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,1,4 and 0 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 105140-20:
(8*1)+(7*0)+(6*5)+(5*1)+(4*4)+(3*0)+(2*2)+(1*0)=63
63 % 10 = 3
So 105140-20-3 is a valid CAS Registry Number.

105140-20-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name methanesulfonate,tetrahexylazanium

1.2 Other means of identification

Product number -
Other names 1-Hexanaminium,N,N,N-trihexyl-,methanesulfonate

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:105140-20-3 SDS

105140-20-3Downstream Products

105140-20-3Relevant academic research and scientific papers

SPECIFIC HYDRATION AND NUCLEOPHILIC REACTIVITY OF ORGANIC ANIONS UNDER PHASE-TRANSFER CATALYSIS AND HOMOGENEOUS CONDITIONS

Landini, Dario,Maia, Angelamaria,Rampoldi, Alessandro

, p. 513 - 518 (2007/10/02)

The effect of specific hydration on the nucleophilic reactivity of the organic anions 3a-i has been studied under PhCl-aqueous NaOH (15-50percent) PTC conditions and in anhydrous chlorobenzene.The sensitivity to the specific solvation, in the order oxanion > carbanion >/= nitranion >/= thianion, can be explained on the basis of the different donor atom tendency.The data provide a useful guide to the choice of the best reaction conditions of these anions under PTC.

Dramatic Effect of the Specific Solvation on the Reactivity of Quaternary Ammonium Fluorides and Poly(hydrogen fluorides), (HF)n*F-, in Media of Low Polarity

Landini, Dario,Maia, Angelamaria,Rampoldi, Alessandro

, p. 328 - 332 (2007/10/02)

A quantitative study of how the intrinsic reactivity (nucleophilicity and basicity) of the fluoride anion of hexyl4N+F- is affected in solvents of low polarity by the specific solvation of a limited number of water molecules has been performed.The nucleophilicity enhancement is extrapolated to be about 3 orders of magnitude by reducing the specific hydration n of the anion from 8.5 to 0.Such enhancement is much higher (ca100 times) than that obtained, under the same conditions, by dehydrating the other halides.The nucleophilicity scale of anhydrous anions found,F- >> Cl- > Br- > I-, reflects those well-known in dipolar aprotic solvents and in the gas phase.Comparison in the same hydration range shows that the basicity of the fluoride anion is much more affected by specific solvation than is its nucleophilicity.Extension of this study to quaternary ammonium poly(hydrogen fluorides) Q+(HF)n*F-, where n = 1, 2, provides the following reactivity scale: F- >> HF2- > H2F3-.The increasing stabilization of F- anion, by interaction with hydrogen fluoride in the sequence F- - -, accounts for the much lower reactivity observed in the case of poly(hydrogen fluorides) with respect to that of the hypothetical anhydrous fluoride (F- : HF2- : H2F3- = 8.5*105 : 1.2*102 : 1).This also explains the different sensitivity of these anions to the specific hydration which decreases in the same order: F- >> HF2- > H2F3-.

A FACILE AND CONVENIENT SYNTHESIS OF LIPOPHILIC TETRAALKYLAMMONIUM OR PHOSPHONIUM HYDROGEN SULFATES

Giorgi, Marco De,Landini, Dario,Maia, Angelamaria,Penso, Michele

, p. 521 - 534 (2007/10/02)

Lipophilic tetraalkylammonium or phosphonium hydrogen sulfates are easily synthesized in very high yields by action of KHSO4 in 10percent aqueous sulfuric acid on the corresponding quaternary azides, the latter being obtained by preparative ion-pair extraction from quaternary methanesulfonates or chlorides.

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