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68400-07-7

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68400-07-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 68400-07-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,4,0 and 0 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 68400-07:
(7*6)+(6*8)+(5*4)+(4*0)+(3*0)+(2*0)+(1*7)=117
117 % 10 = 7
So 68400-07-7 is a valid CAS Registry Number.

68400-07-7Downstream Products

68400-07-7Relevant articles and documents

AGENT FOR DYEING HAIR, CONTAINING AT LEAST ONE ORGANIC SILICON COMPOUND, A COLORING COMPOUND AND A FILM-FORMING, HYDROPHILIC POLYMER

-

, (2021/11/26)

The subject of the present disclosure is a composition for coloring keratinous material, in particular human hair, containing in a cosmetic carrier (a) at least one organic silicon compound selected from silanes having one, two or three silicon atoms, said organic silicon compound further comprising one or more basic chemical functions and one or more hydroxyl groups or hydrolysable groups per molecule,(b) at least one colorant compound from the group of pigments and/or direct dyes, and(c) at least one film-forming hydrophilic polymer.

Non-formaldehyde, crease resistant agent for cotton fabrics based on an organic-inorganic hybrid material

Schramm, Christian,Rinderer, Beate,Tessadri, Richard

, p. 81 - 89 (2014/03/21)

1,2,3,4-Butanetetracarboxylic acid (BTCA) was reacted with (3-aminopropyl)triethoxysilane (APTES) to a poly(amic)acid (PAA). The molar ratios of BTCA and APTES were 1/1 (B/A-1/1), 1/2 (B/A-1/2), 1/3 (B/A-1/3), and 1/4 (B/A-1/4). The as-prepared precursor solution was applied to cotton substrates. After thermal treatment (180°C) the physical-mechanical properties of the cotton samples were tested by means of dry crease recovery angle and tensile strength. For B/A-1/1 treated fabrics a significant improvement of the crease resistance was observed. FT-IR spectra revealed the formation of an imide group and an ester linkage, indicating the cross-linking of the cellulosic material. SEM images showed a smooth surface. As evidenced by TGA data the thermal stability of the cotton samples was not increased. No hydrophobicity could be observed. For B/A-1/3 and (B/A-1/4) modified cotton samples no crease resistant properties were detected. However, enhanced contact angle values were measured. A reaction mechanism for the formation of the ladder-like polysilsesquioxane and the cross-linking reaction is proposed.

Electrospun amino-functionalized PDMS as a novel SPME sorbent for the speciation of inorganic and organometallic arsenic species

Boyaci, Ezel,Horzum, Nesrin,Cagir, Ali,Demir, Mustafa M.,Eroglu, Ahmet E.

, p. 22261 - 22268 (2013/11/06)

Sol-gel based amine-functionalized SPME fibers (PDMS-weak anion exchanger) were prepared and used for direct mode extraction of dimethylarsinic acid (DMA), monomethylarsonic acid (MMA), and arsenate (As(v)) from aqueous solutions followed by HPLC-ICPMS determination. Two different methods of coating were employed: (i) electrospinning and (ii) dip coating. Electrospinning was used for the first time for preparation of sol-gel based SPME fibers and was found to be superior in terms of extracted amount of arsenicals, coating homogeneity, accessibility of amine groups on the surface, and preparation time for a single fiber. Various parameters such as solution pH, extraction time, agitation speed, extraction temperature, and ionic strength were studied. Optimum extraction conditions were determined as pH of 5.0, extraction time of 30 min, agitation speed of 700 rpm, and extraction temperature of 20 °C. Extraction ability of the novel coating decreased by the addition of NaCl as a consequence of the competition between anionic arsenic species and chloride ions for active sites of the weak anion exchanger. This novel sol-gel coating prepared by electrospinning was found to be promising for SPME applications. Vibrational spectroscopy revealed the alignment of PDMS chains by elongational force under electrospinning process. The chain alignment accordingly orients the pendant amino functional groups perpendicular to the fiber surface, which may develop the free active functional groups available to the medium and lead to the enhancement of the extraction performance. Moreover, the proposed coating strategy through electrospinning might be able to break new ground for various applications in analytical chemistry as well as other disciplines. The Royal Society of Chemistry 2013.

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