Interesting facts
Interesting Facts About (3,3,5-Trimethylcyclohexyl) 2-Hydroxybenzoate
(3,3,5-trimethylcyclohexyl) 2-hydroxybenzoate, commonly known as a chemical compound utilized in the realm of organic chemistry, showcases fascinating properties that make it noteworthy in various applications.
Chemical Structure and Characteristics
This compound features an intricate structure that includes:
- Cyclohexyl ring: Providing stability and distinctive reactivity.
- Hydroxy group: Signifying its alcohol character, contributing to its polar nature.
- Benzoate moiety: Highlighting its ester characteristics and potential for specific chemical reactions.
Applications and Utilizations
(3,3,5-trimethylcyclohexyl) 2-hydroxybenzoate is versatile in its applications:
- As an additive: It's primarily used in the formulation of cosmetics and personal care products, enhancing texture and stability.
- In pharmaceuticals: Its properties may be explored for use in drug formulations, providing functional benefits.
- As a flavoring agent: Due to its unique flavor profile, it may find applications in the food industry.
Environmental Considerations
While exploring the benefits, it’s vital to consider its environmental impact:
- The compound's biodegradability and low toxicity are significant factors in its favor.
- Research is continuously conducted to ensure its safe use and to minimize ecological footprints.
In conclusion, the compound (3,3,5-trimethylcyclohexyl) 2-hydroxybenzoate exemplifies the intersection of complexity and utility in organic chemistry. As research progresses, its potential applications may expand, reinforcing its importance in both industrial and academic settings.
Synonyms
Homosalate
118-56-9
Homomenthyl salicylate
Coppertone
3,3,5-TRIMETHYLCYCLOHEXYL SALICYLATE
Heliopan
Heliophan
Filtersol ''A''
m-Homomenthyl salicylate
Homosalato
Homosalatum
3,3,5-Trimethylcyclohexyl 2-hydroxybenzoate
(3,3,5-trimethylcyclohexyl) 2-hydroxybenzoate
Caswell No. 482B
52253-93-7
Benzoic acid, 2-hydroxy-, 3,3,5-trimethylcyclohexyl ester
CCRIS 4885
NSC 164918
Metahomomenthyl salicylate
Homosalatum [INN-Latin]
Homosalato [INN-Spanish]
Salicylic acid, m-homomenthyl ester
EINECS 204-260-8
2-Hydroxybenzoic acid 3,3,5-trimethylcyclohexyl ester
UNII-V06SV4M95S
MFCD00019377
Salicylic Acid 3,3,5-Trimethylcyclohexyl Ester
EPA Pesticide Chemical Code 076603
NSC-164918
V06SV4M95S
Homosalate [USAN:USP:INN]
DTXSID1026241
EC 204-260-8
Salicylic acid, 3,3,5-trimethylcyclohexyl ester
NCGC00091888-01
Homosalatum (INN-Latin)
Homosalato (INN-Spanish)
HOMOSALATE (MART.)
HOMOSALATE [MART.]
HOMOSALATE (USP-RS)
HOMOSALATE [USP-RS]
Homosalate (USAN:USP:INN)
DTXCID606241
Salicylic acid, 3,3,5-trimethylcyclohexyl ester (8CI)
HOMOSALATE (USP IMPURITY)
HOMOSALATE [USP IMPURITY]
HOMOSALATE (USP MONOGRAPH)
HOMOSALATE [USP MONOGRAPH]
Filtrosol A
component of Coppertone
SR-05000001884
Homosalat
Kemester HMS
CAS-118-56-9
Homosalate; Salicylic acid 3,3,5-trimethylcyclohexyl ester; 3,3,5-Trimethylcyclohexyl salicylate
Filtersol''A''
Homosalate (Standard)
HOMOSALATE [MI]
Homosalate (USP/INN)
HOMOSALATE [INN]
Prestwick1_001090
Prestwick2_001090
Prestwick3_001090
HOMOSALATE [USAN]
HOMOSALATE [WHO-DD]
SCHEMBL16207
BSPBio_001140
SPECTRUM1505020
SPBio_003030
BPBio1_001254
Sun Protection Facial SPF 50
CHEMBL1377575
CHEBI:91642
HY-B0928R
MSK3404
3,5-Trimethylcyclohexyl salicylate
HMS1571I22
HMS2093G22
HMS2098I22
HMS3715I22
Pharmakon1600-01505020
component of Coppertone (Salt/Mix)
HY-B0928
3,3,5-Trimethylcyclohexylsalicylate
Tox21_111174
Tox21_202109
Tox21_303082
Homosalate(mixture of cis and trans)
NSC164918
NSC758908
s4572
AKOS015904082
Tox21_111174_1
CCG-213330
DB11064
NSC-758908
NCGC00091888-02
NCGC00091888-03
NCGC00091888-04
NCGC00091888-05
NCGC00091888-06
NCGC00091888-09
NCGC00257063-01
NCGC00259658-01
AS-10409
DA-54062
SY051923
SBI-0206787.P001
AB00514041
NS00009551
Salicylic acid,3,5-trimethylcyclohexyl ester
T2278
Benzoic acid, 3,3,5-trimethylcyclohexyl ester
D04450
E78223
AB00514041_02
EN300-7381967
Q2260189
SR-05000001884-1
SR-05000001884-2
BRD-A34751532-001-03-6
BRD-A34751532-001-04-4
BRD-A34751532-001-06-9
2-hydroxybenzoic acid (3,3,5-trimethylcyclohexyl) ester
Homosalate, United States Pharmacopeia (USP) Reference Standard
Homosalate, Pharmaceutical Secondary Standard; Certified Reference Material
204-260-8
Solubility of (3,3,5-trimethylcyclohexyl) 2-hydroxybenzoate
(3,3,5-trimethylcyclohexyl) 2-hydroxybenzoate, also known as a benzoate ester, exhibits unique solubility characteristics influenced by its structural features. This compound generally tends to be:
In general, the solubility of benzoate esters like (3,3,5-trimethylcyclohexyl) 2-hydroxybenzoate can be summarized by the following principles:
Overall, this compound is more suited for applications in organic phases rather than aqueous environments, making it a versatile candidate in various chemical contexts. This emphasizes the importance of considering both the hydrophobic and hydrophilic characteristics of compounds when assessing solubility.