2215-21-6

Basic information

• Product Name: 3,5-DIISOPROPYLSALICYLIC ACID
• Synonyms: 3,5-DIISOPROPYLSALICYLIC ACID;2-Hydroxy-3,5-diisopropylbenzoic acid;3,5-Diisopropyl-2-hydroxybenzoic acid;3,5-Di-#niso-propyl-2-hydroxybenzoic acid;3,5-DIISOPROPYLSALICYLATE;3,5-DIISOPROPYLSALICYCLICACID;3,5-Diisopropylsalicylic acid,98%;3,5-Diisopropyl-2-hydroxybenzoic acid,3,5-Diisopropylsalicylic acid
• CAS NO: 2215-21-6
• Molecular Formula: C₁₃H₁₈O₃
• Molecular Weight: 222.28
• EINECS: 218-677-8
• Product Categories: Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts
• Mol File: 2215-21-6.mol

Chemical Properties

• Melting Point: 113-115 °C(lit.)
• Boiling Point: 303.46°C (rough estimate)
• Flash Point: 164.3 °C
• Appearance: beige to grey crystalline powder
• Density: 1.1205 (rough estimate)
• Vapor Pressure: 0.0001mmHg at 25°C
• Refractive Index: 1.4740 (estimate)
• Storage Temp.: 4°C
• Solubility: Soluble in organic solvents.
• PKA: 3.21±0.14(Predicted)
• BRN: 2505176
• CAS DataBase Reference: 3,5-DIISOPROPYLSALICYLIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 3,5-DIISOPROPYLSALICYLIC ACID(2215-21-6)
• EPA Substance Registry System: 3,5-DIISOPROPYLSALICYLIC ACID(2215-21-6)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37
• Safety Statements: 22-26-37/39
• WGK Germany: 3
• TSCA: Yes
• Hazardous Substances Data: 2215-21-6(Hazardous Substances Data)

Usage

Uses

Used in Chemical Synthesis:
3,5-Diisopropylsalicylic acid is used as a starting reagent in the synthesis of 2,4-Diisopropyl-phenol at 200°C. It plays a crucial role in the preparation of 3,5-DIISOPROPYLSALICYLIC ACID, which has various applications in the chemical industry.
Used in Coordination Chemistry:
3,5-Diisopropylsalicylic acid is used as a starting reagent in the synthesis of Zn(II) and Cd(II) carboxylate complexes. These complexes have potential applications in various fields, such as catalysis, materials science, and pharmaceuticals.
Used in Metal Complexes:
3,5-Diisopropyl-2-hydroxybenzoic acid plays the role of an OH-inactivating ligand in its complexes with copper(II). This property makes it a valuable component in the development of metal complexes with specific properties and potential applications in various industries.

InChI:InChI=1/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)/p-1

Upstream product

• 67-63-0 isopropyl alcohol 
• 69-72-7 salicylic acid 

Downstream Products

• 49669-40-1 4-carbomethoxyphenyl 3,5-diisopropylsalicylate 
• 33978-55-1 2-hydroxy-3,5-di(propan-2-yl)benzamide 
• 154155-20-1 bis(3,5-diisopropylsalicylato)(1,10-phenanthroline) copper(II) 
• 798570-92-0 [(n-butyl)Sn(O)(3,5-diisopropylsalicylic acid(-H))]6 
• 1265633-46-2 Mn(2,2'-bipyridine)2(3,5-diisopropylsalicylic acid)2 
• 107627-72-5 N-butyl-2-hydroxy-3,5-diisopropylbenzamide 

Relevant articles and documents

Hydrazide salts

A compound having the general formula SPC1 In which R1 , R2, R3 and R4 may be the same or different and represent hydrogen, a straight or branched chain alkyl radical having 1 to 20 carbon atoms, an aralkyl radical having 7 to 20 carbon atoms which may be substituted by one or more alkyl groups having 1 to 4 carbon atoms, or may be of the type: SPC2 Wherein R5 and R6 are each a hydrogen atom or a methyl group, and each R represents the others of R1, R2, R3 and R4, an alkenyl radical having 2 to 20 carbon atoms; a cycloalkyl radical having 5 to 12 carbon atoms which may be substituted by one or more alkyl groups having 1 to 4 carbon atoms; an aryl radical having 6 to 10 carbon atoms; an alkaryl radical having 7 to 12 carbon atoms; a cyclohexyl alkyl radical in which the alkyl moiety has 2 or 3 carbon atoms and the cyclohexenyl ring may contain a methyl group as substituent; an alkenyl cyclohexyl radical in which the alkenyl moiety has 2 or 3 carbon atoms and the cyclohexyl ring may also contain a methyl group as substituent; or a group -OR7 wherein R7 represents an alkyl radical having 1 to 20 carbon atoms, a cycloalkyl radical having 5 to 12 carbon atoms, optionally substituted by one or more alkyl groups having 1 to 4 carbon atoms, an aryl radical having 6 to 10 carbon atoms or an alkenyl radical having 3 to 20 carbon atoms; or any two adjacent radicals R1, R2, R3 and R4 may be joined together to form an aryl ring which may be substituted by one or more alkyl groups having 1 to 20 carbon atoms; X represents an anion; and n is the valency of X, is useful for the extraction of metals from aqueous solutions.