MedKoo Cat#: 591904 | Name: 3'-Hydroxyacetophenone
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Description:

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

3'-Hydroxyacetophenone is a biochemical.

Chemical Structure

3'-Hydroxyacetophenone
3'-Hydroxyacetophenone
CAS#121-71-1

Theoretical Analysis

MedKoo Cat#: 591904

Name: 3'-Hydroxyacetophenone

CAS#: 121-71-1

Chemical Formula: C8H8O2

Exact Mass: 136.0524

Molecular Weight: 136.15

Elemental Analysis: C, 70.58; H, 5.92; O, 23.50

Price and Availability

Size Price Availability Quantity
5g USD 250.00 2 Weeks
10g USD 350.00 2 Weeks
25g USD 450.00 2 Weeks
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Related CAS #
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Synonym
3'-Hydroxyacetophenone; NSC 2440; NSC-2440; NSC2440
IUPAC/Chemical Name
3'-Hydroxyacetophenone
InChi Key
LUJMEECXHPYQOF-UHFFFAOYSA-N
InChi Code
InChI=1S/C8H8O2/c1-6(9)7-3-2-4-8(10)5-7/h2-5,10H,1H3
SMILES Code
CC(C1=CC=CC(O)=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

Preparing Stock Solutions

The following data is based on the product molecular weight 136.15 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
1: Tibbetts KM, Bohinski T, Munkerup K, Tarazkar M, Levis R. Controlling dissociation of alkyl phenyl ketone radical cations in the strong-field regime through hydroxyl substitution position. J Phys Chem A. 2014 Sep 18;118(37):8170-6. doi: 10.1021/jp500874r. Epub 2014 Mar 7. PubMed PMID: 24576102. 2: Zhang R, Ren J, Wang Y, Wu Q, Wang M, Zhu D. Isolation and characterization of a novel Rhodococcus strain with switchable carbonyl reductase and para-acetylphenol hydroxylase activities. J Ind Microbiol Biotechnol. 2013 Jan;40(1):11-20. doi: 10.1007/s10295-012-1199-5. Epub 2012 Sep 27. PubMed PMID: 23014895. 3: Han K, Kim C, Park J, Kim MJ. Chemoenzymatic synthesis of rivastigmine via dynamic kinetic resolution as a key step. J Org Chem. 2010 May 7;75(9):3105-8. doi: 10.1021/jo9027374. PubMed PMID: 20345141.