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Merck
CN

135690

3,5-Diisopropyl-2-hydroxybenzoic acid

98%

Synonym(s):

3,5-Diisopropylsalicylic acid

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About This Item

Linear Formula:
[(CH3)2CH]2C6H2-2-(OH)CO2H
CAS Number:
2215-21-6
Molecular Weight:
222.28
NACRES:
NA.22
PubChem Substance ID:
24848216
UNSPSC Code:
12352100
EC Number:
218-677-8
MDL number:
MFCD00008884

Key Documents

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Product Name

3,5-Diisopropyl-2-hydroxybenzoic acid, 98%

InChI key

XUFUYOGWFZSHGE-UHFFFAOYSA-N

InChI

1S/C13H18O3/c1-7(2)9-5-10(8(3)4)12(14)11(6-9)13(15)16/h5-8,14H,1-4H3,(H,15,16)

SMILES string

CC(C)c1cc(C(C)C)c(O)c(c1)C(O)=O

assay

98%

form

powder

mp

113-115 °C (lit.)

functional group

carboxylic acid

Quality Level

200

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Application

3,5-Diisopropyl-2-hydroxybenzoic acid was used as starting reagent in the synthesis of Zn(II) and Cd(II) carboxylate complexes.

General description

3,5-Diisopropyl-2-hydroxybenzoic acid plays the role of OH-inactivating ligand in its complexes with copper(II).

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H319,H335

Hazard Classifications

Eye Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
0000398205
0000360364
0000355251
0000309844
0000355251

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Yao Yu et al.
European journal of medicinal chemistry, 43(7), 1438-1443 (2007-10-26)
Novel lipophilic platinum(II) complexes (LSPt-1-3), containing 3,5-diisopropylsalicylate (DIPS) as a leaving group and 2NH(3) or 1R,2R-diaminocyclohexane or (4R,5R)-4,5-bis(aminomethyl)-2-isopropyl-1,3-dioxolane as the carrier, have been synthesized, characterized and evaluated in vitro and in vivo. The octanol/water distribution coefficient of the complexes has
Michèle Lamoureux et al.
Journal of fluorescence, 20(3), 631-643 (2010-04-07)
The coordination complexes (DIP)(2)Ru(CH(3)bpyCOOH) and (DIP)(2)Ru(COOHbpyCOOH), where DIP and bpy are diphenylphenanthroline and bispyridine, have been recently proposed as fluorescent markers of nuclear DNA (Musatkina et al., J. Inorg. Biochem. 101:1086-1089, 2007), but no DNA binding investigation and no quantitative
V Brumas et al.
Journal of inorganic biochemistry, 101(4), 565-577 (2007-01-20)
The purpose of this study was to identify the low molecular mass complexes formed between copper(II) and 3,5-diisopropylsalicylic acid (Dips) in physiological conditions. Copper(II)-Dips complex equilibria were determined using glass electrode potentiometry and their solution structures checked by UV-visible (UV-vis)
Eugene O Apostolov et al.
Radiation research, 172(4), 481-492 (2009-09-24)
Gamma radiation is known to induce cell death in several organs. This damage is associated with endonuclease-mediated DNA fragmentation; however, the enzyme that produces the latter and is likely to cause cell death is unknown. To determine whether the most
L F Charles et al.
Journal of materials science. Materials in medicine, 21(6), 1845-1854 (2010-03-20)
Currently, the bone-repair biomaterials market is dominated by high modulus metals and their alloys. The problem of stress-shielding, which results from elastic modulus mismatch between these metallic materials and natural bone, has stimulated increasing research into the development of polymer-ceramic
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