26776-29-4

Basic information

• Product Name: POLY(SEBACIC ANHYDRIDE)
• Synonyms: POLY(SEBACIC ANHYDRIDE);decanedioicacid,homopolymer;sebacic acid homopolymer;Poly(sebacic acid)
• CAS NO: 26776-29-4
• Molecular Formula: C10H18O4
• Molecular Weight: 202.24752
• Mol File: 26776-29-4.mol
• Article Data: 67

Chemical Properties

• Melting Point: 80 °C(lit.)
• Boiling Point: 374.3°Cat760mmHg
• Flash Point: 198.3°C
• Appearance: /
• Density: 1 g/mL at 25 °C(lit.)
• CAS DataBase Reference: POLY(SEBACIC ANHYDRIDE)(CAS DataBase Reference)
• NIST Chemistry Reference: POLY(SEBACIC ANHYDRIDE)(26776-29-4)
• EPA Substance Registry System: POLY(SEBACIC ANHYDRIDE)(26776-29-4)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36
• Hazardous Substances Data: 26776-29-4(Hazardous Substances Data)

Usage

InChI:InChI=1/C10H18O4/c11-9(12)7-5-3-1-2-4-6-8-10(13)14/h1-8H2,(H,11,12)(H,13,14)

Upstream product

• 629-03-8 1 ,6-dibromohexane 
• 540-88-5 acetic acid tert-butyl ester 
• 5169-82-4 4,7-dioxo-1,10-decanedioic acid 
• 112-47-0 1,10-Decanediol 
• 120-92-3 cyclopentanone 
• 1871-96-1 sebaconitrile 
• 13154-30-8 α-nitrocyclodecanone 
• 1209-15-0 furan-2,5-dipropionic acid 
• 64-19-7 acetic acid 
• 110-52-1 1,4-dibromo-butane 
• 60-29-7 diethyl ether 
• 96-01-5 cyclodecane-1,2-dione 
• 7722-84-1 dihydrogen peroxide 
• 74515-86-9 C₃₀H₅₄O₁₂ 

Downstream Products

• 3072-03-5 Sebacinsaeure-dioctadecylester 
• 58296-39-2 1,7-dioxa-cycloheptadecane-8,17-dione 
• 58296-43-8 1,6-dioxa-cyclohexadecane-7,16-dione 
• 96674-05-4 N,N'-didodecyl-decanediamide 
• 14641-31-7 Sebacinsaeure-diundecylester 
• 28891-29-4 Sebacinsaeure-dipentadecylester 
• 26719-49-3 Sebacinsaeure-diheptadecylester 
• 7327-98-2 decanedioic acid mono-(2-ethyl-hexyl ester) 
• 18420-46-7 Diisobutyl-sebacat 
• 6819-09-6 dipentyl sebacate 
• 133318-27-1 decanedioic acid bis-(2-ethyl-butyl ester) 
• 26719-48-2 Sebacinsaeure-di-n-hexadecylester 
• 13379-63-0 1,10-Di-(1-hydroxy-2-naphthyl)-decan-1,10-dion 
• 47510-31-6 S-phenyl decenedithioate 

Relevant articles and documents

A direct synthesis of carboxylic acidsviaplatinum-catalysed hydroxycarbonylation of olefins

The platinum-catalysed hydroxycarbonylation of olefins is reported for the first time. Using a combination of PtCl2/2,2′-bis(tert-butyl(pyridin-2-yl)phosphanyl)-1,1′-binaphthalene (Neolephos) in the presence of sulfuric acid [0.6 M] in acetic acid selective carbonylation of terminal aliphatic olefins proceeds to good yields and selectivities to the corresponding carboxylic acids. Comparing the reactivity of different butenes (iso- andn-butenes), the terminal olefin can be selectively carbonylated.

Molecularization of Bitter Off-Taste Compounds in Pea-Protein Isolates (Pisum sativum L.)

Activity-guided fractionations, combined with taste dilution analyses (TDA), were performed to locate the key compounds contributing to the bitter off-taste of pea-protein isolates (Pisum sativum L.). Purification of the compounds perceived with the highe

PROCESS FOR THE CO-PRODUCTION OF LONG CHAIN AMINO ACIDS AND DIBASIC ACIDS

There is disclosed a process for the co-production of long chain ω-amino acid and long chain dibasic acid, comprising: (1) reacting long chain ketoacid derivative with hydroxylamine or subjecting ketoacid derivative to an ammoximation to yield oxime derivative; (2) subjecting oxime derivative to Beckmann rearrangement to yield a mixture of mixed amide derivatives; (3) hydrolyzing the mixed amide derivatives to produce long chain ω-amino acid and long chain dibasic acid.