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sodium 1-hydroxy-3,7-dimethyloct-6-ene-1-sulphonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

65416-29-7

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65416-29-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65416-29-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,4,1 and 6 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 65416-29:
(7*6)+(6*5)+(5*4)+(4*1)+(3*6)+(2*2)+(1*9)=127
127 % 10 = 7
So 65416-29-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H20O4S.Na/c1-8(2)5-4-6-9(3)7-10(11)15(12,13)14;/h5,9-11H,4,6-7H2,1-3H3,(H,12,13,14);/q;+1/p-1

65416-29-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (+)-(R)-1-hydroxy-3,7-dimethyl-oct-6-ene-1-sulfonic acid , sodium salt

1.2 Other means of identification

Product number -
Other names (+)-(R)-1-Hydroxy-3,7-dimethyl-oct-6-en-1-sulfonsaeure, Natriumsalz

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:65416-29-7 SDS

65416-29-7Downstream Products

65416-29-7Relevant academic research and scientific papers

Liquid-Liquid Extraction Protocol for the Removal of Aldehydes and Highly Reactive Ketones from Mixtures

Boucher, Maria M.,Furigay, Maxwell H.,Quach, Phong K.,Brindle, Cheyenne S.

, p. 1394 - 1403 (2017/09/23)

The reaction of the bisulfite ion with aldehydes to form charged bisulfite adducts is a well-established method for the purification of aldehydes. This reaction has been modified to create a convenient liquid-liquid extraction method for the removal of aldehydes from mixtures. The use of a water-miscible solvent allows the reaction to occur during a simple 30 s shaking protocol by increasing the contact between the bisulfite ion and the aldehyde. The introduction of an immiscible solvent allows for the extraction of the uncharged organic components away from the bisulfite adduct. The developed protocol is applicable to a wide range of aldehydes, including sterically hindered neopentyl aldehydes. Sterically unhindered cyclic and linear ketones, as well as highly electrophilic ketones, are also removed using this protocol. The mild conditions tolerate a wide range of functional groups, allowing for excellent aldehyde contaminant removal rates with high levels of recovery of the desired component.

Direct reductive alkylation of amine hydrochlorides with aldehyde bisulfite adducts

Barniol-Xicota, Marta,Turcu, Andreea L.,Codony, Sandra,Escolano, Carmen,Vázquez, Santiago

supporting information, p. 2548 - 2550 (2014/05/06)

A mild procedure for the direct reaction of aromatic and aliphatic aldehyde bisulfite adducts with primary and secondary amine hydrochlorides in the presence of sodium cyanoborohydride in methanol is reported.

A NOVEL AND VERSATILE SEPARATION METHOD FOR ALDEHYDES

Ohta, Shunsaku,Okamoto, Masao

, p. 1917 - 1919 (2007/10/02)

An aqueous solution of sodium ε-amino-n-caproate can be used for efficient and simple separation of aldehydes, overcoming the difficulties associated with the NaHSO3 method.Keywords - separation of aldehydes; Schiff base of amino acid; ω-amino acid; sodium ε-amino-n-caproate; sodium bisulfite adduct of aldehydes

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