MedKoo Cat#: 591811 | Name: N-Allylaniline
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Description:

WARNING: This product is for research use only, not for human or veterinary use.

N-Allylaniline is used as a seperation material.

Chemical Structure

N-Allylaniline
N-Allylaniline
CAS#589-09-3

Theoretical Analysis

MedKoo Cat#: 591811

Name: N-Allylaniline

CAS#: 589-09-3

Chemical Formula: C9H11N

Exact Mass: 133.0891

Molecular Weight: 133.19

Elemental Analysis: C, 81.16; H, 8.32; N, 10.52

Price and Availability

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5g USD 260.00
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Related CAS #
No Data
Synonym
N-Allylaniline; AI3-10028; AI3 10028; AI310028
IUPAC/Chemical Name
Benzenamine, N-2-propenyl-
InChi Key
LQFLWKPCQITJIH-UHFFFAOYSA-N
InChi Code
InChI=1S/C9H11N/c1-2-8-10-9-6-4-3-5-7-9/h2-7,10H,1,8H2
SMILES Code
C=CCNC1=CC=CC=C1
Appearance
Solid powder
Purity
>98% (or refer to the Certificate of Analysis)
Shipping Condition
Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage Condition
Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).
Solubility
Soluble in DMSO
Shelf Life
>3 years if stored properly
Drug Formulation
This drug may be formulated in DMSO
Stock Solution Storage
0 - 4 C for short term (days to weeks), or -20 C for long term (months).
HS Tariff Code
2934.99.03.00
More Info
Product Data
Biological target:
N-Allylaniline is used as a seperation material.
In vitro activity:
TBD
In vivo activity:
TBD

Preparing Stock Solutions

The following data is based on the product molecular weight 133.19 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
Formulation protocol:
TBD
In vitro protocol:
TBD
In vivo protocol:
TBD
1: Dana M, Luliński P, Maciejewska D. Synthesis of homoveratric acid-imprinted polymers and their evaluation as selective separation materials. Molecules. 2011 May 5;16(5):3826-44. doi: 10.3390/molecules16053826. PubMed PMID: 21546882. 2: Mossine VV, Barnes CL, Mawhinney TP. Disordered hydrogen bonding in N-(1-deoxy-beta-D-fructopyranos-1-yl)-N-allylaniline. Carbohydr Res. 2009 May 12;344(7):948-51. doi: 10.1016/j.carres.2009.02.017. Epub 2009 Feb 25. PubMed PMID: 19345935. 3: Leroi C, Bertin D, Dufils PE, Gigmes D, Marque S, Tordo P, Couturier JL, Guerret O, Ciufolini MA. Alkoxyamine-mediated radical synthesis of indolinones and indolines. Org Lett. 2003 Dec 25;5(26):4943-5. PubMed PMID: 14682735. 4: Inoue S, Takamatsu N, Kishi Y. [Synthetic studies on echinulin and realted natural products. I. Acid-catalyzed amino-Claisen rearrangement of N-allylaniline and N,N-diallylaniline derivatives (author's transl)]. Yakugaku Zasshi. 1977 May;97(5):553-7. Japanese. PubMed PMID: 560461.