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135690

Sigma-Aldrich

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
EC Number:
218-677-8
MDL number:
MFCD00008884
UNSPSC Code:
12352100
PubChem Substance ID:
24848216
NACRES:
NA.22

Assay

98%

form

powder

mp

113-115 °C (lit.)

SMILES string

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

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)

InChI key

XUFUYOGWFZSHGE-UHFFFAOYSA-N

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General description

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

Application

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

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H319,H335

Hazard Classifications

Eye Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

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)

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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
Monika Homoncik et al.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis, 14(2), 131-138 (2003-03-13)
We examined the influence of 3,5-diisopropylsalicylic acid (3,5-DIPS) and calcium(II)3 (3,5-diisopropylsalicylate)6 (H2 O)6 [Ca(II)3 (3,5-DIPS)6 ], a new activator of calcium-dependent calmodulin-triggered nitric oxide synthase, on thrombin-induced platelet P-selectin expression. Citrated whole blood samples were incubated with either ethanol vehicle
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)
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