P-Acetotoluide | CAS#103-89-9 | biochemical

MedKoo Cat#: 591738 | Name: P-Acetotoluide

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Description:

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

P-Acetotoluide is a biochemical.

Chemical Structure

P-Acetotoluide

CAS#103-89-9

Theoretical Analysis

MedKoo Cat#: 591738

Name: P-Acetotoluide

CAS#: 103-89-9

Chemical Formula: C9H11NO

Exact Mass: 149.0841

Molecular Weight: 149.19

Elemental Analysis: C, 72.46; H, 7.43; N, 9.39; O, 10.72

Price and Availability

Size	Price	Availability	Quantity
100g	USD 450.00	2 Weeks

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Related CAS #

No Data

Synonym

P-Acetotoluide; NSC 7644; NSC-7644; NSC7644

IUPAC/Chemical Name

4'-Methylacetanilide

InChi Key

YICAMJWHIUMFDI-UHFFFAOYSA-N

InChi Code

InChI=1S/C9H11NO/c1-7-3-5-9(6-4-7)10-8(2)11/h3-6H,1-2H3,(H,10,11)

SMILES Code

CC(NC1=CC=C(C)C=C1)=O

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

Product Data

Instruction

View handling instruction

Biological target:

P-Acetotoluide is a biochemical.

In vitro activity:

TBD

In vivo activity:

TBD

Preparing Stock Solutions

The following data is based on the product molecular weight 149.19 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.

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: Giri SN, Siegel DM. Comparative studies of the covalent binding of [14C]-2-chloro-4-acetotoluidide by liver and kidney slices of the starling. J Appl Toxicol. 1991 Jun;11(3):223-8. PubMed PMID: 1918797. 2: Giri SN, Siegel DM. Characterization of covalent binding of [14C]-2-chloro-4-acetotoluidide to microsomes of starling liver and kidney. J Biochem Toxicol. 1991 Summer;6(2):137-45. PubMed PMID: 1941900. 3: Apostolou A, Wing K. Sensitization potential of the avicides 3-chloro-p-toluidine and 2-chloro-4-acetotoluidide. J Environ Pathol Toxicol. 1979 Jul-Aug;2(6):1543-4. PubMed PMID: 528858. 4: Apostolou A. Phototoxicity study of the avicides 3-chloro-p-toluidine and 2-chloro-4-acetotoluidide in guinea pigs. Vet Hum Toxicol. 1979 Jun;21(3):163. PubMed PMID: 462733. 5: Katchen B, Dancik S, Millington G. Percutaneous penetration and metabolism of topical (14C)flutamide in men. J Invest Dermatol. 1976 Jun;66(6):379-82. PubMed PMID: 932487. 6: Katchen B, Buxbaum S. Disposition of a new, nonsteroid, antiandrogen, alpha,alpha,alpha-trifluoro-2-methyl-4'-nitro-m-propionotoluidide (Flutamide), in men following a single oral 200 mg dose. J Clin Endocrinol Metab. 1975 Aug;41(2):373-9. PubMed PMID: 1159048. 7: Apostolou A, Peoples SA. Toxicity of the avicide 2-chloro-4-acetotoluidide in rats: a comparison with its nonacetylated form 3-chloro-p-toluidine. Toxicol Appl Pharmacol. 1971 Mar;18(3):517-21. PubMed PMID: 5569826. 8: Yasue M, Sakakibara J, Yano K. [Reaction o-, m- and p-acetotoluidide with 2-propanol in concentrated sulfuric acid]. Yakugaku Zasshi. 1968 Dec;88(12):1616-9. Japanese. PubMed PMID: 5715527.