3'-Hydroxyacetophenone
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MedKoo CAT#: 591904

CAS#: 121-71-1

Description: 3'-Hydroxyacetophenone is a biochemical.


Chemical Structure

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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
5.0g USD 260.0 2 Weeks
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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

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

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*When preparing stock solutions always use the batch-specific molecular weight of the product found on the vial label and SDS / CoA (available online).

Reconstitution Calculator

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Dilution Calculator

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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.