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Butanedioic acid, bis(4-nitrophenyl) ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

33109-58-9

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33109-58-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 33109-58-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,1,0 and 9 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 33109-58:
(7*3)+(6*3)+(5*1)+(4*0)+(3*9)+(2*5)+(1*8)=89
89 % 10 = 9
So 33109-58-9 is a valid CAS Registry Number.

33109-58-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name bis(4-nitrophenyl) butanedioate

1.2 Other means of identification

Product number -
Other names succinic acid bis(p-nitrophenyl 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:33109-58-9 SDS

33109-58-9Relevant academic research and scientific papers

From macro to micro to nano: The development of a novel lysine based hydrogel platform and enzyme triggered self-assembly of macro hydrogel into nanogel

Wu, De-Qun,Wu, Jun,Qin, Xiao-Hong,Chu, Chih-Chang

, p. 2286 - 2294 (2015/03/18)

A novel L-lysine based multifunctional crosslinker family was developed and utilized to fabricate a 100% pure poly(ester amide) (PEA) hydrogel with unique structure via a novel gelation strategy in a single and rapid step. Enzyme triggered biodegradation

ABSORBABLE BRANCHED POLYESTERS AND POLYURETHANES

-

Paragraph 0121-0123, (2014/05/25)

The present invention relates to the discovery of a new class of hydrolysable isocyanates, hydrolysable branched polyols and branched absorbable polyesters and polyurethanes prepared therefrom. The resultant absorbable polymers are useful for drug delivery, stents, highly porous foam, reticulated foam, tissue engineering, tissue adhesives, adhesion prevention, bone wax formulations, medical device coatings, surface modifying agents and other implantable medical devices. In addition, these absorbable polymers can have a controlled hydrolytic degradation profile.

PROCESS FOR PREPARATION OF SUCCINYLCHOLINE CHLORIDE

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Page/Page column 8, (2014/03/21)

The invention discloses a novel process for preparation of succinylcholine chloride via transesterification of succinic acid diester with choline chloride.

Synthesis and characterization of functionalized water soluble cationic poly(ester amide)s

Pang, Xuan,Wu, Jun,Reinhart-King, Cynthia,Chu, Chih-Chang

scheme or table, p. 3758 - 3766 (2011/11/12)

A new family of positively charged, water soluble and functional amino acid-based poly(ester amide)s (Arg-AG PEA) consisting of four building blocks (L-Arginine, DL-2-Allylglycine, oligoethylene glycol, and aliphatic diacid) were synthesized by the soluti

BIODEGRADABLE WATER SOLUBLE POLYMERS

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Page/Page column 46, (2010/11/29)

The invention provides biodegradable, water soluble PEA, PEUR and PEU carrier polymers, which can be used to conjugate, and thereby stabilize and/or solublize, bioactive agents via polar uncharged or charged groups and activated ester or amino groups cont

Synthesis, conformation, and binding properties of cyclodextrin homo- and heterodimers connected through their secondary sides

Venema, Fokke,Nelissen, Hubertus F. M.,Berthault, Patrick,Birlirakis, Nicolaos,Rowan, Alan E.,Feiters, Martinus C.,Nolte, Roeland J. M.

, p. 2237 - 2250 (2007/10/03)

The synthesis of homo- and heterocyclodextrin (CD) dimers, containing two CD moieties that are linked through their secondary sides by alipathic or 2,2'-bipyridyl spacers is described. In these dimers, the glucose units to which the spacers are linked hav

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