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268402

Sigma-Aldrich

4-Isopropylbenzoic acid

≥96%

Synonym(s):

Cumic acid, Cuminic acid

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About This Item

Linear Formula:
(CH3)2CHC6H4CO2H
CAS Number:
536-66-3
Molecular Weight:
164.20
EC Number:
208-642-5
MDL number:
MFCD00002564
UNSPSC Code:
12352100
PubChem Substance ID:
24856271
NACRES:
NA.22

Assay

≥96%

mp

117-120 °C (lit.)

solubility

alcohol: soluble(lit.)
diethyl ether: soluble(lit.)
sulfuric acid: soluble(lit.)
water: slightly soluble(lit.)

SMILES string

CC(C)c1ccc(cc1)C(O)=O

InChI

1S/C10H12O2/c1-7(2)8-3-5-9(6-4-8)10(11)12/h3-7H,1-2H3,(H,11,12)

InChI key

CKMXAIVXVKGGFM-UHFFFAOYSA-N

Related Categories

Application

4-Isopropylbenzoic acid (cuminic acid) was used in the synthesis of three new triorganotin carboxylates bearing methyl, butyl and phenyl substituents at tin, respectively. The products were fully characterized by spectroscopic and thermal techniques, with regard to the coordination number of tin atom, in solution and in the solid state.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Bruno Gaillet et al.
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Fast and efficient production of recombinant proteins for structural and functional studies is a crucial issue for research and for industry. To this end, we have developed an efficient system to generate in less than 2 months, starting from the
Angiolini L, et al.
Journal of Organometallic Chemistry, 691(9), 1965-1972 (2006)
R W Eaton
Journal of bacteriology, 178(5), 1351-1362 (1996-03-01)
Pseudomonas putida F1 utilizes p-cumate (p-isopropylbenzoate) as a growth substrate by means of an eight-step catabolic pathway. A 35.75-kb DNA segment, within which the cmt operon encoding the catabolism of p-cumate is located, was cloned as four separate overlapping restriction
G J Pass et al.
Xenobiotica; the fate of foreign compounds in biological systems, 32(5), 383-397 (2002-06-18)
1. p-Cymene is an aromatic monoterpene found in the leaves of Eucalyptus spp. and is ingested in the diet of two marsupial folivores, the brushtail possum (Trichosurus vulpecula) and koala (Phascolarctos cinereus). The metabolism of p-cymene by liver microsomes from
L G Puskás et al.
DNA sequence : the journal of DNA sequencing and mapping, 11(1-2), 9-20 (2000-07-21)
Rhodopseudomonas palustris utilizes p-cumate as a carbon source both under anaerobic light and aerobic dark conditions. A gene cluster was isolated whose sequence showed high homology to genes which have been implicated the degradation of p-cumate in Pseudomonas pitida. Seven
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