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11-Aminoundecanoic acid

11-Aminoundecanoic acid Structure
CAS No.
2432-99-7
Chemical Name:
11-Aminoundecanoic acid
Synonyms
nci-c50613;H-11-Aun-OH;NH2-(CH2)10-COOH;ω-aminoundecanoic;11-Aminoundecansure;aminoundecanoicacid;11-Aminoundecanoic a;11-Amino-undecansaeure;11-amino-undecanoicaci;11-AMINOUNDECYLIC ACID
CBNumber:
CB4187611
Molecular Formula:
C11H23NO2
Molecular Weight:
201.31
MOL File:
2432-99-7.mol
MSDS File:
SDS
Modify Date:
2023/5/4 17:34:36

11-Aminoundecanoic acid 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
form Crystalline Powder
pka 4.78±0.10(Predicted)
color White
Water Solubility 2 g/L (20 ºC)
BRN 1767291
InChIKey GUOSQNAUYHMCRU-UHFFFAOYSA-N
LogP -0.16 at 20℃
CAS DataBase Reference 2432-99-7(CAS DataBase Reference)
IARC 3 (Vol. 39, Sup 7) 1987
EPA Substance Registry System 11-Aminoundecanoic acid (2432-99-7)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H302
Precautionary statements  P280-P305+P351+P338
Risk Statements  52
Safety Statements  24/25
WGK Germany  1
RTECS  YQ2293000
HS Code  29224995
Toxicity LDLo orl-rat: 14,700 mg/kg NTPTR* NTP-TR-216,82

11-Aminoundecanoic acid price More Price(3)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) A82605 11-Aminoundecanoic acid 97% 2432-99-7 100G ₹4719.7 2022-06-14 Buy
Sigma-Aldrich(India) A82605 11-Aminoundecanoic acid 97% 2432-99-7 500G ₹14310.65 2022-06-14 Buy
Sigma-Aldrich(India) 8.01228 11-Aminoundecanoic acid for synthesis 2432-99-7 250G ₹12020 2022-06-14 Buy
Product number Packaging Price Buy
A82605 100G ₹4719.7 Buy
A82605 500G ₹14310.65 Buy
8.01228 250G ₹12020 Buy

11-Aminoundecanoic acid Chemical Properties,Uses,Production

Chemical Properties

11-Aminoundecanoic acid is a solid.

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 Description

White crystalline solid or powder.

Air & Water Reactions

Insoluble in water.

Reactivity Profile

11-Aminoundecanoic acid is incompatible with strong oxidizing agents, strong acids and strong bases.

Fire Hazard

Flash point data for 11-Aminoundecanoic acid are not available; however, 11-Aminoundecanoic acid is probably combustible.

Safety Profile

Poison by ingestion. Questionable carcinogen with experimental carcinogenic and neoplastigenic data. Mutation data reported. When heated to decomposition it emits toxic fumes of NOx,.

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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 OMEGA-AMINOUNDECANOIC ACID OMEGA-AMINOUNDECYLIC ACID 11-Aminoundecanoic aCld 11-aminoundecanoicacid(11-aa) Undecanoic acid, 11-amino- 11-Aminoundecansure aminoundecanoicacid nci-c50613 11-Aminoundecanoic acid,97% H-11-Aun-OH 11-Aminoundecanoic a 11-AMinoundecanoic acid 11-AMinoundecanoic acid 11-AMinoundecanoic acid, 97% 100GR 11-AMINOUNDECANOIC ACID PURUM 98% 11-Aminoundecanoic acid USP/EP/BP ω-aminoundecanoic 2432-99-7 11-Aminoundecanoic acid 2432-99-7 2434-99-7 NH2CH210CO2H AMINE Peptide Synthesis Linear Core Amino Acids Specialty Synthesis Unnatural Amino Acid Derivatives Linear Core Amino Acids Peptide Synthesis Unnatural Amino Acid Derivatives