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didodecyl [R-(R*,R*)]-tartrate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

66584-29-0

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66584-29-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66584-29-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,5,8 and 4 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 66584-29:
(7*6)+(6*6)+(5*5)+(4*8)+(3*4)+(2*2)+(1*9)=160
160 % 10 = 0
So 66584-29-0 is a valid CAS Registry Number.
InChI:InChI=1/C28H54O6/c1-3-5-7-9-11-13-15-17-19-21-23-33-27(31)25(29)26(30)28(32)34-24-22-20-18-16-14-12-10-8-6-4-2/h25-26,29-30H,3-24H2,1-2H3/t25-,26-/m1/s1

66584-29-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R,3R)-didodecyl tartarate

1.2 Other means of identification

Product number -
Other names Lg-tartaric acid didodecyl ester

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:66584-29-0 SDS

66584-29-0Downstream Products

66584-29-0Relevant academic research and scientific papers

Preparation, physicochemical properties, and transfection activities of tartaric acid-based cationic lipids as effective nonviral gene delivery vectors

Wan, Ning,Jia, Yi-Yang,Hou, Yi-Lin,Ma, Xi-Xi,He, Yong-Sheng,Li, Chen,Zhou, Si-Yuan,Zhang, Bang-Le

, p. 1112 - 1120 (2016/07/19)

In this work two novel cationic lipids using natural tartaric acid as linking backbone were synthesized. These cationic lipids were simply constructed by tartaric acid backbone using head group 6-aminocaproic acid and saturated hydrocarbon chains dodecanol (T-C12-AH) or hexadecanol (T-C16-AH). The physicochemical properties, gel electrophoresis, transfection activities, and cytotoxicity of cationic liposomes were tested. The optimum formulation for T-C12-AH and T-C16-AH was at cationic lipid/dioleoylphosphatidylethanolamine (DOPE) molar ratio of 1:0.5 and 1:2, respectively, and N/P charge molar ratio of 1:1 and 1:1, respectively. Under optimized conditions, T-C12-AH and T-C16-AH showed effective gene transfection capabilities, superior or comparable to that of commercially available transfecting reagent 3β-[N-(N′,N′-dimethylaminoethyl)carbamoyl]cholesterol (DC-Chol) and N-[2,3-dioleoyloxypropyl]-N,N,N-trimethylammonium chloride (DOTAP). The results demonstrated that the two novel tartaric acid-based cationic lipids exhibited low toxicity and efficient transfection performance, offering an excellent prospect as nonviral vectors for gene delivery.

Dicarboxylic acid esters as transdermal permeation enhancers: Effects of chain number and geometric isomers

Novotny, Michal,Hrabalek, Alexandr,Janusova, Barbora,Novotny, Jakub,Vavrova, Katerina

supporting information; experimental part, p. 344 - 347 (2011/02/26)

A series of transdermal permeation enhancers based on dicarboxylic acid esters was studied. Single-chain amphiphiles were markedly more effective than the double-chain ones. Monododecyl maleate, that is a cis derivative, was a more potent enhancer than its trans isomer, while the activity of succinates strongly depended on the donor vehicle. No difference between diastereoisomeric tartaric and meso-tartaric acid derivatives was found.

Enantioselective distribution of amino-alcohols in a liquid-liquid two-phase system containing dialkyl L-tartrate and boric acid

Abe,Shoji,Kobayashi,Qing,Asai,Nishizawa

, p. 262 - 265 (2007/10/02)

Racemic amino-alcohols such as pindolol, propranolol, alprenolol and bucumolol enantiomers exhibited different distribution behaviors in a two-phase system consisting of a chloroform solution of didodecyl L-tartrate and an aqueous solution of boric acid. It seemed that a borate complex of the 1,2-diol group of the tartrate and the amino-alcohol was formed in the system. In the case of pindolol, one enantiomer was preferentially extracted into the organic phase (x 2.20) at equilibrium.

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