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13590-97-1

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    Cas No: 13590-97-1

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13590-97-1 Usage

General Description

Dodecylguanidine hydrochloride is a chemical compound that belongs to the class of guanidines and is derived from dodecylamine and cyanamide. It is commonly used as an antiseptic and disinfectant in various applications, including in the healthcare and personal care industries. It exhibits strong antimicrobial properties and is effective against a wide range of bacteria, fungi, and viruses. Dodecylguanidine hydrochloride can be found in various formulations, including as an ingredient in mouthwashes, skin cleansers, and surface disinfectants. It is known for its ability to disrupt the cell membranes of microorganisms, leading to their destruction, making it a valuable compound in the fight against infections.

Check Digit Verification of cas no

The CAS Registry Mumber 13590-97-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,5,9 and 0 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 13590-97:
(7*1)+(6*3)+(5*5)+(4*9)+(3*0)+(2*9)+(1*7)=111
111 % 10 = 1
So 13590-97-1 is a valid CAS Registry Number.
InChI:InChI=1/C13H29N3.ClH/c1-2-3-4-5-6-7-8-9-10-11-12-16-13(14)15;/h2-12H2,1H3,(H4,14,15,16);1H

13590-97-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name DODECYLGUANIDINE HYDROCHLORIDE

1.2 Other means of identification

Product number -
Other names metasoldgh

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:13590-97-1 SDS

13590-97-1Downstream Products

13590-97-1Relevant articles and documents

Guanidinium vs. ammonium surfactants in soft-templating approaches: Nanostructured silica and zwitterionic i-silica from complementary precursor-surfactant ion pairs

El Hankari, Samir,Hesemann, Peter

, p. 5288 - 5298 (2012)

We investigated the behaviour of guanidinium and ammonium surfactants as structure-directing agents in template-directed hydrolysis/polycondensation processes. For this purpose, a series of guanidinium surfactants was synthesised from long-chain-substituted primary amines. In a first series of experiments, we compared nanostructured silicas obtained by means of template-directed hydrolysis/polycondensation reactions of TEOS in the presence of either guanidinium- or ammonium-based surfactants. We observed that typical MCM-41-type silicas displaying a 2D hexagonal architecture were obtained in the presence of ammonium surfactants such as cetyltrimethylammonium bromide (CTAB). In contrast, the use of guanidinium surfactants led to the formation of hollow silica spheres or spherical silica nanoparticles. Secondly, we investigated the use of ammonium and guanidinium surfactants in the formation of periodic mesoporous organosilicas containing ionic groups (i-silica). In particular, we studied template-directed hydrolysis/polycondensation reactions of zwitterionic ammonium sulfonate and ammonium carboxylate precursors. We observed that both reactions involving the ammonium sulfonate precursor yielded structured i-silicas. In contrast, hydrolysis/polycondensation reactions of the ammonium carboxylate precursor afforded structured materials only in the presence of the guanidinium surfactant, whereas amorphous materials were obtained in the presence of CTAB. This result reflects specific surfactant-precursor interactions and suggests that the nature of both surfactant and precursor determine the formation of i-silica materials displaying regular architectures on a mesoscopic length scale. We compared ammonium and guanidinium surfactants as structure-directing agents in soft templating syntheses of nanostructured and hybrid-silica-based ionic substructures (i-silicas). Nanostructured i-silicas exist due to specific carboxylate precursor/guanidinium surfactant interactions. Results suggest that nanostructured silica hybrid materials can be obtained from complementary precursor-surfactant pairs. Copyright

Compounding method for dozine

-

Paragraph 0045; 0046; 0047; 0048; 0049, (2017/11/30)

The invention provides a compounding method for dozine. The method comprises the following steps: taking guanidine hydrochloride as an initial raw material to react with chlorododecane, thereby acquiring a midbody A; adding an alkali aqueous solution into the midbody A for reaction; adding glacial acetic acid for reaction; performing after-treatment, thereby acquiring a target product dozine. The compounding method is characterized by easily acquired raw materials, few reaction steps, mild reaction condition, simplicity in operation and higher yield and is an environment-friendly compounding method, so that the compounding method is suitable for large-scale industrial production and has wide application prospect and market potential.

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