11-Aminoundecanoic acid

11-Aminoundecanoic acid Basic information
Product Name:11-Aminoundecanoic acid
Synonyms:11-AMINOUNDECANOIC ACID;11-AMINOUNDECYLIC ACID;11-amino-undecanoicaci;11-AMINOUNDECANOIC ACID FOR SYNTHESIS;11-amino-n-undecanoic acid;11-Amino-undecansaeure;11-Aminoundecanoic acid≥ 99% (Titration);NH2-(CH2)10-COOH
CAS:2432-99-7
MF:C11H23NO2
MW:201.31
EINECS:219-417-6
Product Categories:Linear Core Amino Acids;Peptide Synthesis;Unnatural Amino Acid Derivatives
Mol File:2432-99-7.mol
11-Aminoundecanoic acid Structure
11-Aminoundecanoic acid Chemical Properties
Melting point 188-191 °C (lit.)
Boiling point 339.24°C (rough estimate)
density 0.9896 (rough estimate)
refractive index 1.4420 (estimate)
storage temp. Store below +30°C.
solubility 2g/l
pka4.78±0.10(Predicted)
form Crystalline Powder
color White
Water Solubility 2 g/L (20 ºC)
BRN 1767291
InChIKeyGUOSQNAUYHMCRU-UHFFFAOYSA-N
LogP-0.16 at 20℃
CAS DataBase Reference2432-99-7(CAS DataBase Reference)
IARC3 (Vol. 39, Sup 7) 1987
EPA Substance Registry System11-Aminoundecanoic acid (2432-99-7)
Safety Information
Risk Statements 52
Safety Statements 24/25
WGK Germany 1
RTECS YQ2293000
HS Code 29224995
Hazardous Substances Data2432-99-7(Hazardous Substances Data)
ToxicityLDLo orl-rat: 14,700 mg/kg NTPTR* NTP-TR-216,82
MSDS Information
ProviderLanguage
11-Aminoundecanoic acid English
SigmaAldrich English
ACROS English
11-Aminoundecanoic acid Usage And Synthesis
DescriptionAminoundecanoic acid can be used as a PROTAC linker in the synthesis of PROTACs. Aminoundecanoic acid is an alkane chain with terminal carboxlic acid and amine groups. The amino group (NH2) is reactive with carboxylic acids, activated NHS esters, carbonyls (ketone, aldehyde) etc. The terminal carboxylic acid can react with primary amine groups of activated NHS ester to form a stable amide bond.
Chemical PropertiesWhite crystalline powder
Chemical Properties11-Aminoundecanoic acid is a solid.
Uses11-Aminoundecanoic Acid is used to prepare thapsigargin analogues targeting apoptosis to prostatic cancer cells. It is also used to synthesize N-carboxyalkylpeptides containing extended alkyl residues at P1''as matrix metalloproteinase inhibitors.
DefinitionChEBI: 11-Aminoundecanoic acid is a medium-chain fatty acid.
Preparation|?-Aminoundecanoic acid is normally prepared from castor oil (glycerol triricinoleate). Firstly the castor oil is subjected to methanolysis to yield the methyl ester of ricinoleic acid and then the following route is used:

2432-99-7 synthesis


In the first step, the pyrolysis of methyl ricinoleate is carried out at about 500??C; the principal products are n-heptaldehyde and methyl undecylenate. The latter is hydrolysed to give undecylenic acid which is treated with hydrogen bromide in a non-polar solvent in the presence of a peroxide. Under these conditions, reverse Markownikoff addition occurs and the main product is |?-bromoundecanoic acid. This product is then treated with ammonia to give |?-aminoundecanoic acid, which is a crystalline solid, m.p. 189??C.

General DescriptionWhite crystalline solid or powder.
Air & Water ReactionsInsoluble in water.
Reactivity Profile11-Aminoundecanoic acid is incompatible with strong oxidizing agents, strong acids and strong bases.
Fire HazardFlash point data for 11-Aminoundecanoic acid are not available; however, 11-Aminoundecanoic acid is probably combustible.
Flammability and ExplosibilityNonflammable
Safety ProfilePoison by ingestion. Questionable carcinogen with experimental carcinogenic and neoplastigenic data. Mutation data reported. When heated to decomposition it emits toxic fumes of NOx,.
11-Aminoundecanoic acid Preparation Products And Raw materials
Preparation Products11-HYDROXYUNDECANOIC ACID-->11-AMINO-1-UNDECANOL-->N-(11-Bromoundecyl)carbamic acid tert-butyl ester-->Undecanoic acid, 11-[[(1,1-dimethylethoxy)carbonyl]amino]-, 2,5-dioxo-1-pyrrolidinyl ester-->11-(METHACRYLOYLAMINO)UNDECANOIC ACID
SALOR-INT L333263-1EA n-Hendecane Hendecanoic acid SALOR-INT L333301-1EA Ethyl 2-(Chlorosulfonyl)acetate Testosterone undecanoate Ascoric Acid 2-AMINODIETHYLMALONATE 11-Aminoundecanoic acid Stearic acid Folic acid 6-Aminocaproic acid N-ALPHA-T-BOC-11-AMINOUNDECANOIC ACID,T-BUTOXYCARBONYL-11-AMINOUNDECANOIC ACID,BOC-11-AMINOUNDECANOIC ACID ETHYL 3-AMINOCROTONATE DDMAU 2-(2-Aminothiazol-4-yl)glyoxylic acid Epristeride Citric acid

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