Interesting facts
Exploring 2-ethylhexane-1,3-diol
2-ethylhexane-1,3-diol is a fascinating compound that plays a significant role in various industrial applications. As a diol (a type of alcohol that contains two hydroxyl groups), it provides unique properties that make it valuable in chemical synthesis and formulation.
Key Characteristics
- Versatility: This compound serves as an intermediate in the production of plastics, including polyurethanes, which are crucial in a wide range of applications from furniture to automotive parts.
- Moisturizing Agent: Its hydroxyl groups contribute to its ability to retain moisture, making it a potential ingredient in personal care products like creams and lotions.
- Stabilizer: 2-ethylhexane-1,3-diol is also used as a stabilizer in paints and coatings, helping to improve their performance and longevity.
Interesting Applications
This compound is not just useful in industrial settings; its properties allow for various interesting applications:
- Plasticizers: It is often utilized in the formulation of plasticizers, which enhance the flexibility and durability of plastics.
- Pharmaceuticals: In the pharmaceutical industry, its dual alcohol functionality can be leveraged in drug formulation, potentially contributing to improved solubility and bioavailability.
- Biodegradable Alternatives: With growing concerns about environmental impact, compounds like 2-ethylhexane-1,3-diol are being investigated as biodegradable alternatives to traditional petroleum-based solvents.
In summary, 2-ethylhexane-1,3-diol stands out not just for its chemical structure but for its wide range of applications and contributions to various industries. As we continue to innovate in chemistry, understanding and utilizing compounds like this can lead to more sustainable and effective solutions in everyday products.
Synonyms
2-ETHYL-1,3-HEXANEDIOL
94-96-2
Ethohexadiol
2-Ethylhexane-1,3-diol
Ethyl hexanediol
1,3-Hexanediol, 2-ethyl-
Octylene glycol
etohexadiol
Repellent 612
Carbide 6-12
Ethylhexylene glycol
2-Ethyl-1,3-hexandiol
Rutgers 612
6-12 insect repellent
6-12-Insect repellent
Diol-Kyowa 8
Ethohexadiol [USP]
Caswell No. 445
2-Ethyl-3-propyl-1,3-propanediol
2-Ethyl-1,3-hexylene glycol
2-ethylhexanediol
3-Hydroxymethyl-n-heptan-4-ol
ENT 375
CCRIS 4034
Compound 6-12 insect repellent
HSDB 1716
UNII-M9JGK7U88V
EH diol
NSC 3881
NSC-3881
EINECS 202-377-9
BRN 1735324
Ethyl hexylene glycol
DTXSID4025292
AI3-00375
Compound 6-12, insect repellent
2-Ethylhexanediol-1,3
ETHOHEXADIOL [MI]
MFCD00004578
ETHOHEXADIOL [HSDB]
Ethyl-1,3-hexane diol-2
M9JGK7U88V
ETHOHEXADIOL [MART.]
ETHOHEXADIOL [WHO-DD]
DTXCID405292
CHEBI:34273
NSC3881
EC 202-377-9
4-01-00-02597 (Beilstein Handbook Reference)
Ethohexadiol (USP)
NCGC00091575-01
Diol-Kyowa 8; Ethohexadiol; NSC 3881
ETHOHEXADIOL (MART.)
(2RS,3RS;2RS,3SR)-2-ETHYLHEXANE-1,3-DIOL
Latka 612 [Czech]
CAS-94-96-2
Latka 612
EPA Pesticide Chemical Code 041001
DiolKyowa 8
Carbide 612
2Ethyl1,3hexanediol
612Insect repellent
612 insect repellent
3Hydroxymethylnheptan4ol
2Ethyl1,3hexylene glycol
REPELLANT 612
2-ethyl-1,3-hexane diol
2-ethyl-hexane-1,3-diol
2Ethyl3propyl1,3propanediol
RUTGERS 6-12
SCHEMBL38007
Compound 612 insect repellent
LATKA 612 (Czechoslovakia)
WLN: QY3&Y2&1Q
ETHYL HEXANEDIOL [INCI]
CHEMBL1451179
Tox21_111152
Tox21_202003
Tox21_303253
AKOS002313502
AKOS016051411
Tox21_111152_1
DB13826
COMPOUND 6-12 INSECT REPELLANT
NCGC00091575-02
NCGC00091575-03
NCGC00256943-01
NCGC00259552-01
AS-80897
2-Ethyl-1,3-hexanediol, analytical standard
E0119
NS00005681
SBI-0654054.0001
Q992192
SR-01000944444
SR-01000944444-1
BRD-A55455283-001-01-3
Solubility of 2-ethylhexane-1,3-diol
2-ethylhexane-1,3-diol, a diol compound, exhibits notable solubility characteristics due to the presence of multiple -OH (hydroxyl) groups. Here are some important points regarding its solubility:
In summary, the solubility of 2-ethylhexane-1,3-diol is significantly influenced by its hydroxyl groups, allowing it to dissolve well in both polar and some non-polar environments, making it a useful compound in various chemical processes.