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Sodium 2-octyldodecyl sulfate is a double-tail sulfate surfactant with unique properties that make it valuable in various applications.

78204-54-3

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78204-54-3 Usage

Uses

Used in Surface Chemistry and Colloids Research:
Sodium 2-octyldodecyl sulfate is used as a surfactant in the study of surface chemistry and colloids for its ability to lower surface tension and stabilize colloidal systems. This allows researchers to investigate the behavior of these systems and develop new applications in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 78204-54-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,2,0 and 4 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 78204-54:
(7*7)+(6*8)+(5*2)+(4*0)+(3*4)+(2*5)+(1*4)=133
133 % 10 = 3
So 78204-54-3 is a valid CAS Registry Number.
InChI:InChI=1/C20H42O4S.Na/c1-3-5-7-9-11-12-14-16-18-20(19-24-25(21,22)23)17-15-13-10-8-6-4-2;/h20H,3-19H2,1-2H3,(H,21,22,23);/q;+1/p-1

78204-54-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name sodium,2-octyldodecyl sulfate

1.2 Other means of identification

Product number -
Other names Sodium 2-octyl-1-docecyl sulfate

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:78204-54-3 SDS

78204-54-3Upstream product

78204-54-3Downstream Products

78204-54-3Relevant academic research and scientific papers

API ionic liquids: Probing the effect of counterion structure on physical form and lipid solubility

Benameur, Hassan,Ford, Leigh,Nguyen, Tri-Hung,Porter, Christopher J. H.,Scammells, Peter J.,Tay, Erin,Williams, Hywel D.

, p. 12788 - 12799 (2020/04/22)

Lipid based formulations (LBFs) are extensively utilised as an enabling technology in drug delivery. The use of ionic liquids (ILs) or lipophilic salts (LS) in drug delivery has also garnered considerable interest due to unique solubility properties. Conversion of active pharmaceutical ingredients (API) to ILs by pairing with an appropriately lipophilic counterion has been shown to decrease melting point of the salt complex and improve solubility in LBFs. However, the relationship between the structure of the counterion, the physicochemical properties of the resulting salts and solubility in LBFs has not been systematically explored. This study investigates the relationship between alkyl sulfate counterion structure and melting temperature (Tm or Tg) in addition to LBF solubility, utilizing cinnarizine and lumefantrine as model weakly basic APIs. Three series of structurally diverse alkyl sulfate counterions were chosen to probe this relationship. Pairing cinnarizine and lumefantrine with a majority of these alkyl sulfate counterions resulted in a reduction in melting temperature and enhanced solubility in model medium chain and long chain LBFs. The chain length of the alkyl sulfate plays a crucial role in performance, and consistently branched alkyl sulfate counterions perform better than straight chain alkyl sulfate counterions, as predicted. Most interestingly, trends in counterion performance were found to be consistent across two APIs with disparate chemical structures. The findings from this study will facilitate the design of counterions which enhance solubility of ionisable drugs and unlock the potential to develop compounds previously restrained by poor solubility.

Softener composition

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Page/Page column 8, (2008/06/13)

A softener composition that can impart a high softening effect to clothes irrespective of the state of rinsing water, which contains (a) a compound of formula (1) below, (b) a compound of formula (3) below, and (c) a specific anionic surfactant, wherein the mole ratios between the components (a), (b) and (c) satisfy the following relationship: [(a)+(b)]/(c)=9/1 to 4/6; and wherein R1 represents a C13-36 alkyl group or the like, R10 and R12 respectively represent a C8-36 alkyl group or the like, R2, R11 and R13 respectively represent a C1-6 alkylene group, R3, R4, and R14 respectively represent a C1-3 alkyl group or the like, A, D and E respectively represent —COO—, —CONH— or the like, and “a”, “c” and “d” respectively denote 0 or 1.

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