Name | 1,11-Undecanedicarboxylic acid |
Synonyms | UNDECANE-1 Brassylic acid BRASSYLIC ACID tridecanedioate TRIDECANDIOIC ACID Tridecanedioic acid TRIDECANEDIOIC ACID 11-DECARBOXYLIC ACID 1,13-TRIDECANEDIOIC ACID TRIDECANE-1,13-DIOIC ACID 1,11-Undecanedicarboxylic acid 1,11-UNDECANEDICARBOXYLIC ACID |
CAS | 505-52-2 |
EINECS | 208-011-4 |
InChI | InChI=1/C13H24O4/c14-12(15)10-8-6-4-2-1-3-5-7-9-11-13(16)17/h1-11H2,(H,14,15)(H,16,17)/p-2 |
InChIKey | DXNCZXXFRKPEPY-UHFFFAOYSA-N |
Molecular Formula | C13H24O4 |
Molar Mass | 244.33 |
Density | 1.15 g/cm3 (25℃) |
Melting Point | 112-114°C(lit.) |
Boling Point | 415.5°C (rough estimate) |
Flash Point | 223.5°C |
Water Solubility | Insoluble |
Solubility | DMSO (Slightly), Methanol (Slightly) |
Vapor Presure | 0Pa at 20℃ |
Appearance | White crystalline powder |
Color | White to Off-White |
pKa | 4.48±0.10(Predicted) |
Storage Condition | Sealed in dry,Room Temperature |
Refractive Index | 1.4453 (estimate) |
MDL | MFCD00002740 |
Physical and Chemical Properties | Melting point 112-114°C water-soluble Insoluble |
Use | Used in the production of high-grade flavor, fragrance and artificial musk-T, Hot Melt Adhesive and engineering plastics, advanced food packaging materials, is also the main raw material of high-grade nylon 1313 |
Hazard Symbols | Xi - Irritant |
Risk Codes | 36/37/38 - Irritating to eyes, respiratory system and skin. |
Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S37/39 - Wear suitable gloves and eye/face protection |
WGK Germany | 3 |
TSCA | Yes |
HS Code | 29171990 |
LogP | 3.3 at 25℃ |
NIST chemical information | Information provided by: webbook.nist.gov (external link) |
EPA chemical information | Information provided by: ofmpub.epa.gov (external link) |
biological activity | 1,11-Undecanedicarboxylic acid (Tridecanedioic acid, Brassylic acid, Brassilic acid) is an uncommon odd-numbered dicarboxylic acid, which appears in the urine of children with neonatal adrenal leukodystrophy and cerebral hepatorenal syndrome, and is a new marker of peroxidase disease disorder. |
use | perfume: used to synthesize ethylenyl tridecarboxylate. In terms of plastics:(1) It can be used as a component for the production of copolyamides with good transparency, heat resistance and mechanical properties;(2) It can be used as a raw material for polyether amide resins with good heat resistance and molding processability;(3) As a raw material for adjusting image recording and heat sensitive plates;(4) As a raw material for photosensitive polyamide resins; surfactants and lubricants:(1) As a raw material for fiber softeners;(2) It can be used as a lubricant raw material for metal processing. Photographic and recording materials:(1) improving the durability of the metal magnetic film for magnetic recording materials;(2) as a lubricant for metal processing;(3) The mixed aqueous solution with pyrazole derivatives is a metal treatment agent having a good anti-rust effect. Metal compounds: polynuclear metal complexes used as liquid crystal alignment agents. In terms of antibacterial agents: non-medical antibacterial agents composed of dicarboxylic acid compounds and dicarboxylic acid mono-alkali metal salts. Other aspects:(1) pharmaceutical and pesticide intermediates;(2) plasticizer raw materials. It is used to produce high-grade flavors, spices and artificial musk-T, hot melt adhesive and engineering plastics, high-grade food packaging materials, and is also the main raw material for high-grade nylon 1313 |
production method | American Emery Company used special rapeseed oil to extract erucic acid, which was obtained by ozone oxidation and redecomposition. Japanese mining companies use self-produced straight-chain alkanes as raw materials to produce by fermentation. In addition, in addition to linear alkanes, the raw materials can also be synthesized from linear olefins, saturated or unsaturated fatty acids, hexadecanoates, etc. |