11-Aminoundecanoic acid

 CAS No.: 2432-99-7  Cat No.: BP-500079  Purity: ≥ 99% (Titration) 4.5  

11-Aminoundecanoic acid is a unique ω-amino acid, recognized for its role in polymer synthesis and material science research. The long-chain structure, terminated by an amino group, imparts hydrophobic properties, making it an ideal candidate for studying lipid interactions and membrane dynamics. Soluble in organic solvents, it serves as a precursor in the production of specialized nylons and biodegradable polymers. Moreover, its derivative forms have application potential in the design of antifouling coatings and biocompatible materials, contributing significantly to innovative material engineering studies.

11-Aminoundecanoic acid

Structure of 2432-99-7

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Molecular Formula
C11H23NO2
Molecular Weight
201.31
Appearance
White to off-white powder

* For research and manufacturing use only. Not for human or clinical use.

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Purity
≥ 99% (Titration)
Solubility
In DMSO: 3.33 mg/mL (16.54 mM; ultrasonic and adjust pH to 2 with HCl)<br/>In H2O: < 0.1 mg/mL (ultrasonic;adjust pH to 3 with HCl) (insoluble)
Appearance
White to off-white powder
Storage
Store at 2-8 °C
Shipping
Room temperature in continental US; may vary elsewhere.
IUPACName
11-aminoundecanoic acid
Synonyms
ω-Aminoundecanoic acid; Undecanoic acid, 11-amino-; 11-Aminoundecylic acid; 11-amino-undecanoic acid; H-11-Aun-OH
Boiling Point
334.9 °C at 760 mmHg
Melting Point
187-191 °C
Density
0.965 g/cm3
InChI Key
GUOSQNAUYHMCRU-UHFFFAOYSA-N
InChI
InChI=1S/C11H23NO2/c12-10-8-6-4-2-1-3-5-7-9-11(13)14/h1-10,12H2,(H,13,14)
Canonical SMILES
C(CCCCCN)CCCCC(=O)O
2. Carcinogenesis Bioassay of 11-Aminoundecanoic Acid (CAS No. 2432-99-7) in F344 Rats and B6C3F1 Mice
National Toxicology Program Natl Toxicol Program Tech Rep Ser. 1982 May;216:1-116.
11-Aminoundecanoic acid is the monomer used in the manufacture of the polyamide, nylon-11. Aminoundecanoic acid is synthesized through a series of reactions from ricinoleic acid isolated from castor bean oil. Nylon-11 is used in automobile parts, industrial fabrics (e.g. filter bags, work clothes, and netting), and brushes because of its resistance to vibration and shock and its stability when in contact with fuels. Nylon-11 resins are approved by the U.S. Food and Drug Administration for use on food contact films. A carcinogenesis bioassay of 11-aminoundecanoic acid was carried out by administering diets containing 7,500 or 15,000 ppm of 11-aminoundecanoic acid to F344 rats and B6C3F1 mice. Groups of 50 rats and 50 mice of either sex were administered the test chemical for 104 weeks (rats) or 103 weeks (mice). Controls consisted of 50 untreated rats and 50 untreated mice of each sex. Nonneoplastic effects included dose-related decreases in mean body weight gain and survival for male rats and for mice of each sex; a dose-related increased incidence of hyperplasia of the transitional epithelium of the kidney and urinary bladder in rats of each sex; and mineralization of the kidney in dosed mice of each sex. Neoplastic nodules of the liver in dosed male rats (control 1/50, 2%; low dose 9/50, 18%; high dose 8/50, 16%; P<0.01) and transitional-cell carcinomas of the urinary bladder in high-dose male rats (control 0/48, 0%; low dose 0/48, 0%; high dose 7/49, 14%: P<0.01) were observed at significantly increased incidences compared with controls. Malignant lymphomas occurred at a significantly (P<0.05) increased rate in low-dose male mice (control 2/50, 4%; low dose 9/50, 18%; high dose 4/50, 8%). Under the conditions of this bioassay, 11-aminoundecanoic acid was carcinogenic for male F344 rats, inducing neoplastic nodules in the liver and transitional-cell carcinomas in the urinary bladder. The test chemical was not carcinogenic for female F344 rats. No clear evidence was found for the carcinogenicity of 11-aminoundecanoic acid in B6C3F1 mice of either sex, although the increase in malignant lymphoma in male mice may have been associated with administration of 11-aminoundecanoic acid. Levels of Evidence of Carcinogenicity: Male Rats: Positive Female Rats: Negative Male Mice: Equivocal Female Mice: Negative
3. Isolation and genomic analysis of 11-aminoundecanoic acid-degrading bacterium Pseudomonas sp. JG-B from nylon 11 enrichment culture
Jocelyn Gatz-Schrupp, Peter Deckard, Benjamin Hufford, Steven Ly, Peter Tupa, Hisako Masuda J Genomics. 2020 Jan 25;8:16-20. doi: 10.7150/jgen.42095. eCollection 2020.
Nylon 11 is a polymer synthesized from 11-aminoundecanoic acid, and widely used in commercial manufacturing. In this study, we describe the isolation of the first organism capable of metabolizing 11-aminoundecanoic acid from nylon 11 enrichment culture. The strain shows rapid growth on 11-aminoundecanoic acid as a sole source of carbon, nitrogen, and energy. Furthermore, the genome sequence of strain JG-B was deciphered and shown to belong to genus Pseudomonas. Many genes encoding putative extracellular hydrolases, as well as homologues of nylon 6 hydrolases (NylB and NylA) were identified, suggesting the metabolic versatility and possibility that this organism could also depolymerase nylon 11 polymers.
ConcentrationVolumeMass1 mg5 mg10 mg
1 mM4.9675 mL24.8373 mL49.6746 mL
5 mM0.9935 mL4.9675 mL9.9349 mL
10 mM0.4967 mL2.4837 mL4.9675 mL

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It is commonly abbreviated as: C1V1 = C2V2

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Tip: Chemical formula is case sensitive. C22H30N4O c22h30n40
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