We collect cookies for vital website function and to better serve our customers. By continuing to browse you agree to the storing of cookies on your device. See our privacy policy for details.

Undecanoic Acid

Item № 19721
CAS № 112-37-8
Purity ≥95%
product image
                (CAS 112-37-8)
SIZE PRICE QUANTITY SUBTOTAL
CART TOTAL
     1 g $25.00 0.00
     5 g $56.00 0.00

Pricing updated 2019-07-17. Prices are subject to change without notice.

Description
Synonyms
  • NSC 7885
  • Hendecanoic Acid
  • Undecylic Acid

Undecanoic acid is a saturated fatty acid containing eleven carbons (C11:0). It is cytotoxic to certain filamentous fungi and is used to study fungal mechanisms of resistance.1,2 Undecanoic acid is also used to acylate larger molecules.3

Recommended Products

Related Products
View Related Product Categories
Technical Information
Formal Name
undecanoic acid
CAS Number
112-37-8
Synonyms
  • NSC 7885
  • Hendecanoic Acid
  • Undecylic Acid
Molecular Formula
C11H22O2
Formula Weight
186.3
Purity
≥95%
Formulation
A crystalline solid
SMILES
OC(CCCCCCCCCC)=O
InChI Code
InChI=1S/C11H22O2/c1-2-3-4-5-6-7-8-9-10-11(12)13/h2-10H2,1H3,(H,12,13)
InChI Key
ZDPHROOEEOARMN-UHFFFAOYSA-N
Side Chain Carbon Sum
11:0

Warning - this product is not for human or veterinary use.

Shipping & Storage
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
Stability
≥ 1 year
Downloads & Resources
Product Downloads

Download Product Insert

Download Safety Data Sheet (SDS)

Download free InChI Key generation software

Additional Information

View the Cayman Structure Database for chemical structure definitions for many Cayman products

Get Batch-Specific Data and Documents by Batch Number

Provide batch numbers separated by commas to download or request available product inserts, QC sheets, certificates of analysis, data pack, and GC-MS data.

References & Product Citations
Product Description References

1. Brito-Madurro, A.G., Cuadros-Orellana, S., Martinez-Rossi, N.M., et al. Undecanoic acid resistance in filamentous fungi: Identification and linkage mapping of the Aspergillus nidulans udaA gene J.Gen.Appl.Microbiol. 51(1), 47-49 (2005).

2. Paiao, F.G., Segato, F., Cursino-Santos, J.R., et al. Analysis of Trichophyton rubrum gene expression in response to cytotoxic drugs FEMS Microbiology Letters 271(2), 180-186 (2007).

3. Bogatcheva, E., Dubuisson, T., Protopopova, M., et al. Chemical modification of capuramycins to enhance antibacterial activity Journal of Antimicrobial Chemotherapy 66(3), 578-587 (2011).

Technical Support
Contact Us
  • Toll Free Phone (USA and Canada Only): (888) 526-5351
  • Direct Phone: (734) 975-3888
Cayman Contract Services

We work with scientists to accelerate their research, drug discovery, and drug development needs through our expertise in the following areas:

Cayman Chemical

1180 East Ellsworth Road

Ann Arbor, Michigan 48108 USA

Toll Free: (800) 364-9897

(USA and Canada Only)

Fax: (734) 971-3640