Grundinformationen
- Standard-SMILES
CC(C#N)(CCC(=O)O)N=NC(C)(C#N)CCC(=O)O- InChIKey
VFXXTYGQYWRHJP-UHFFFAOYSA-N- Summenformel
- C12H16N4O4
- Durchschnittliche Molmasse
- 280,28 g/mol
- Monoisotopische Masse
- 280,11715499
Namen und Bezeichner
- Bevorzugter Name
- 4,4-Azobis(4-cyanovaleric acid)
- IUPAC
- 4-[(4-carboxy-2-cyanobutan-2-yl)diazenyl]-4-cyanopentanoic acid
- Lokaler Name
- 4,4'-Azobis[4-cyanvalerian]sure
- Englischer Name
- 4,4'-Azobis(4-cyanovaleric acid)
- Summenformel
- C12H16N4O4
- Molmasse
- 280.28
Namen und Synonyme
Weitere Namen anzeigen
Datenbank-Bezeichner
- CAS
1041193-98-9、2638-94-0- PubChem CID
- 92938
- DTXSID
DTXSID3044629- ChEMBL
CHEMBL3185815- EC Number
- 220-135-0
- Nikkaji
- J3.697.119C、J80.531I
Eigenschaften
Berechnete Struktureigenschaften
- XLogP
- 0,3
- Polarare Oberfläche (TPSA)
- 147 Ų
- H-Brücken-Donoren
- 2
- H-Brücken-Akzeptoren
- 8
- Frei drehbare Bindungen
- 8
- Schwere Atome
- 20
- Formalladung
- 0
- Komplexität
- 466
Experimentelle und physikochemische Eigenschaften
Physical Description
Wet Solid
White solid; [Sigma-Aldrich MSDS]
Physikochemische Eigenschaften
- Schmelzpunkt
- 118 · 118-125 °C (dec.) (lit.)
- Siedepunkt
- 423 °C · 423°C (rough estimate)
- Dichte
- 1.2464 · 1.2464 (rough estimate)
- Brechungsindex
- 1.6081 · 1.6081 (estimate)
- storage temp.
- 2 · 2-8°C
- Löslichkeit
- DMSO (Slightly), Methanol (Slightly)
- Aggregatzustand
- Solid
- pka
- 3.98 · 3.98±0.10(Predicted)
- Farbe
- White
- Wasserlöslichkeit
- Soluble in water.
- BRN
- 1729856 · 1729856
- InChI
- 1S/C12H16N4O4/c1-11(7-13,5-3-9(17)18)15-16-12(2,8-14)6-4-10(19)20/h3-6H2,1-2H3,(H,17,18)(H,19,20)/b16-15+
- InChIKey
- VFXXTYGQYWRHJP-FOCLMDBBSA-N
- SMILES
- CC(CCC(O)=O)(\N=N\C(C)(CCC(O)=O)C#N)C#N
- LogP
- 0.8 at · 0.8 at 23℃
- CAS Datenbank
- 2638 · 2638-94-0(CAS DataBase Reference)
- NIST chemische Informationen
- 4 · 4,4'-Azo-bis(4-cyanopentanoic acid)(2638-94-0)
- EPA chemische Informationen
- 4 · 4,4'-Azobis(4-cyanovaleric acid) (2638-94-0)
Sicherheit und Regulatorisches
GHS-Klassifizierung
GHS Classification
This chemical does not meet GHS hazard criteria for 12.4% (30 of 241) of reports.
Danger
H228 (24.5%): Flammable solid [Danger Flammable solids]
P210, P234, P235, P240, P241, P280, P370+P378, P403, P410, P411, P420, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 241 reports by companies from 8 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Gefahrenhinweise
Regulatory Information
Chemical: Pentanoic acid, 4,4'-azobis[4-cyano-
Pentanoic acid, 4,4'-(1,2-diazenediyl)bis[4-cyano- is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of Pentanoic acid, 4,4'-(1,2-diazenediyl)bis[4-cyano- are required to report information about their production and use of this chemical to the EPA under the Toxic Substances Control Act (TSCA). (40 eCFR Part 711)
Status: Active Update: 03-09-2019 https://echa.europa.eu/registration-dossier/-/registered-dossier/22344
Pentanoic acid, 4,4'-azobis[4-cyano-: Does not have an individual approval but may be used as a component in a product covered by a group standard. It is not approved for use as a chemical in its own right.
Sicherheitsdaten
- F
- 4.4-8
- wgk
- 2
- tsca
- TSCA listed
- ridadr
- UN 1325 4.1/PG 2
- hs_code
- 29270000
- RTECS-Nr.
- YV6190500
- risk_code
- 11
- Toxizität
- LD50 ipr-mus: 666 mg/kg 85JCAE -,922,86
- hazard_code
- F
- safety_code
- 15-16-22-24/25-36
- hazard_class
- 4.1
- Speicherklasse
- 5.2 - Organic peroxides and self-reacting hazardous materials
- Hazard Classifications
- Self-react. D
Chemie und Industrie
Verwendung und Herstellung
General Manufacturing Information
Plastics Material and Resin Manufacturing
Pentanoic acid, 4,4'-(1,2-diazenediyl)bis[4-cyano-: ACTIVE
Anwendungen
Verwenden4,4'-Azobis(4-cyanovaleric acid) is used as a free radical imitator in polymer synthesis such as polyvinyl chloride, polyacrylonitrile, polyvinyl alcohol and synthetic fibers. It is utilized for both heterogeneous and homogenous free-radical polymerizations, and as an initiator in reversible addition-fragmentation chain transfer polymerization (RAFT). It is also used as a blowing agent for plastics and elastomers.
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