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dodecyl gallate

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Identification
Molecular formula
C19H28O5
CAS number
1166-52-5
IUPAC name
dodecyl 3,4,5-trihydroxybenzoate
State
State

At room temperature, dodecyl gallate is in a solid state, typically in the form of crystalline powder.

Melting point (Celsius)
101.00
Melting point (Kelvin)
374.15
Boiling point (Celsius)
334.50
Boiling point (Kelvin)
607.65
General information
Molecular weight
338.44g/mol
Molar mass
338.4380g/mol
Density
1.0650g/cm3
Appearence

Dodecyl gallate appears as a white to off-white crystalline powder. It is generally odorless and is known for its antioxidant properties.

Comment on solubility

Solubility of Dodecyl 3,4,5-trihydroxybenzoate

Dodecyl 3,4,5-trihydroxybenzoate is a compound known for its interesting solubility profile, which can be influenced by various factors. Understanding its solubility behavior is crucial in applications such as pharmaceuticals and cosmetics. Here are some key points to consider:

  • Solvent Types: Dodecyl 3,4,5-trihydroxybenzoate tends to exhibit varying solubility in different solvents, including:
    • Polar solvents: Water solubility is generally low due to the hydrophobic dodecyl chain.
    • Non-polar solvents: It is more soluble in organic solvents such as ethanol or hexane, where the hydrophobic interaction is favorable.
  • Temperature Effects: Solubility can increase with temperature, as higher temperatures can enhance molecular interactions in solvents.
  • pH Influence: The presence of hydroxyl groups in the molecule can lead to changes in solubility based on the pH of the solution, affecting hydrogen bonding and ionization.

To summarize, the solubility of dodecyl 3,4,5-trihydroxybenzoate is primarily driven by its structural features and environmental conditions. As stated, “the solubility of a compound is as dynamic as the conditions under which it exists.” Understanding these aspects is vital for maximizing its usefulness in various applications.

Interesting facts

Facts about Dodecyl 3,4,5-Trihydroxybenzoate

Dodecyl 3,4,5-trihydroxybenzoate, often referred to as a surfactant and emulsifier in various applications, is a fascinating compound with multiple uses in the fields of chemistry and industry. Here are some interesting facts:

  • Chemical Structure: This compound features a dodecyl chain providing hydrophobic characteristics, whereas the 3,4,5-trihydroxy substituents on the benzoate moiety introduce hydrophilic properties, making it an effective surfactant.
  • Applications:
    • Widely used in cosmetics and personal care products for its emulsifying properties.
    • Functions as a corrosion inhibitor in various industrial applications.
    • Acts as a stabilizer in food additives, enhancing texture and moisture retention.
  • Biocompatibility: Due to its relatively non-toxic profile, dodecyl 3,4,5-trihydroxybenzoate is often selected for formulations intended for sensitive skin and biodegradable applications.
  • Research Insights: Ongoing studies are investigating the biochemical pathways affected by this compound, highlighting its potential roles in drug delivery systems and therapeutic formulations. Some researchers are exploring its antioxidant properties as well.
  • Innovative Uses: Its unique ability to form complexes with other molecules is being considered for use in various nanotechnology applications, such as drug carriers and in modifying surfaces for enhanced properties.
  • Environmental Considerations: Interest in its biodegradability and environmental impact is prompting studies aimed at understanding its breakdown products and overall ecological footprint.

In summary, dodecyl 3,4,5-trihydroxybenzoate is not only a versatile compound with applications across several industries but also an area of intriguing research that continues to unveil its potential. This compound epitomizes the intersection of chemistry, biology, and industrial innovation.

Synonyms
Dodecyl gallate
Lauryl gallate
Dodecyl 3,4,5-trihydroxybenzoate
BENZOIC ACID, 3,4,5-TRIHYDROXY-, DODECYL ESTER
n-Dodecyl gallate
n-dodecylgallate
CCRIS 5568
GALLIC ACID LAURYL ESTER
Gallic acid n-dodecyl ester
EINECS 214-620-6
BRN 2701981
DTXSID0048189
UNII-45612DY463
NSC-133463
Gallic acid, n-dodecyl ester
INS NO.312
DODECYL GALLATE [MART.]
DTXCID5028164
INS-312
Dodecyl-3,4,5-trihydroxybenzoate
4-10-00-02006 (Beilstein Handbook Reference)
DODECYL ESTER OF GALLIC ACID
DODECYL GALLATE [EP MONOGRAPH]
E-312
DODECYL GALLATE (MART.)
N-DODECYL (OR LAURYL) ESTER OF 3,4,5-TRIHYDROXYBENZOIC ACID
DODECYL GALLATE (EP MONOGRAPH)
Dodecyl 3
Dodecyl gallic acid
N-Dodecylgallic acid
45-Trihydroxybenzoate
45-Trihydroxybenzoic acid
DODECYL GALLATE [INCI]
Dodecyl 3,4,5-trihydroxybenzoic acid
rpwfjamtcnsjkk-uhfffaoysa-n
1166-52-5
Nipagallin LA
Progallin LA
Gallic acid, dodecyl ester
Gallic acid, lauryl ester
Lauryl 3,4,5-trihydroxybenzoate
Dodecylester kyseliny gallove
NSC 133463
Gallic acid-dodecyl ester
MFCD00002195
E312
CHEMBL16121
Lauryl Gallate(Dodecyl Gallate)
3,4,5-Trihydroxybenzoic acid, dodecyl ester
NSC133463
45612DY463
Gallic Acid Dodecyl Ester
antioxidant E 312
antioxidant E-312
E 312 antioxidant
E-312 antioxidant
CAS-1166-52-5
Dodecylester kyseliny gallove [Czech]
dodecylgallat
Dodecyl gallate (Standard)
SCHEMBL36820
149030-04-6
BIDD:ER0314
Lauryl 3,5-trihydroxybenzoate
WLN: QR BQ CQ EVO12
CHEBI:175304
Gallic acid, dodecyl ester (8CI)
BCP15874
Tox21_202724
Tox21_303487
BDBM50093887
s6229
AKOS001482340
dodecyl 3,4,5-tris(oxidanyl)benzoate
FL33333
GS-3008
HY-124082R
NCGC00257297-01
NCGC00260272-01
SY048252
DB-108599
HY-124082
3,4,5-Trihydroxy-benzoic acid dodecyl ester
Benzoic acid,4,5-trihydroxy-, dodecyl ester
CS-0084125
G0015
Lauryl gallate, analytical reference material
NS00013651
D70249
Lauryl gallate, antioxidant, >=99.0% (HPLC)
A803659
Dodecyl gallate; Dodecyl 3,4,5-trihydroxybenzoate
Q418209
3,4,5-TRIHYDROXYBENZOIC ACID DODECYL ESTER
Dodecyl gallate, European Pharmacopoeia (EP) Reference Standard