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Dibutyl phthalate - >99%(GC), high purity , CAS No.84-74-2, Activator of TRPA1
Basic Description
Synonyms
Palatinol C | Genoplast B | n-Butyl phthalate | Phthalic acid di-n-butyl ester | Phthalic acid dibutyl ester | Butyl phthalate | Di-n-butyl phthalate | Benzene-1,2-dicarboxylic acid di-n-butylester
Specifications & Purity
Moligand™, ≥99%(GC)
Storage Temp
Argon charged
Shipped In
Normal
Grade
Moligand™
Action Type
ACTIVATOR
Mechanism of action
Activator of TRPA1
Product Description
Dibutyl phthalate (DBP) is most commonly used as a plasticizer in a variety of household products. It has the ability to leach and evaporate into the environment while using or disposing of these products. Therefore, studies are being conducted to assess its toxic and apoptotic effects.Studies have also indicated that exposure to high doses of DBP may interfere with progesterone and estradiol production.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Taxonomic Classification
Kingdom
Organic compounds
Superclass
Benzenoids
Class
Benzene and substituted derivatives
Subclass
Benzoic acids and derivatives
Intermediate Tree Nodes
Not available
Direct Parent
Benzoic acid esters
Alternative Parents
Benzoyl derivatives Dicarboxylic acids and derivatives Carboxylic acid esters Organooxygen compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic homomonocyclic compounds
Substituents
Benzoate ester - Benzoyl - Dicarboxylic acid or derivatives - Carboxylic acid ester - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Aromatic homomonocyclic compound
Description
This compound belongs to the class of organic compounds known as benzoic acid esters. These are ester derivatives of benzoic acid.
External Descriptors
Insect repellents - Phthalates
Data sources
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
Associated Targets(Human)
Associated Targets(non-human)
Mechanisms of Action
Mechanism of Action
Action Type
target ID
Target Name
Target Type
Target Organism
Binding Site Name
References
Names and Identifiers
IUPAC Name
dibutyl benzene-1,2-dicarboxylate
INCHI
InChI=1S/C16H22O4/c1-3-5-11-19-15(17)13-9-7-8-10-14(13)16(18)20-12-6-4-2/h7-10H,3-6,11-12H2,1-2H3
InChIKey
DOIRQSBPFJWKBE-UHFFFAOYSA-N
Smiles
CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC
Isomeric SMILES
CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC
WGK Germany
2
RTECS
TI0875000
UN Number
3082
Packing Group
III
Molecular Weight
278.35
Beilstein
1914064
Reaxy-Rn
1914064
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1914064&ln=
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
Chemical and Physical Properties
Solubility
Soluble in water (0.4 mg/ml at 20 °C), ethanol. Very soluble in ether, acetone, and benzene.
Sensitivity
Moisture sensitive.
Refractive Index
1.49
Flash Point(°F)
339.8 °F
Flash Point(°C)
171℃
Boil Point(°C)
340°C
Melt Point(°C)
-3.5°C
Molecular Weight
278.340 g/mol
XLogP3
4.700
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
4
Rotatable Bond Count
10
Exact Mass
278.152 Da
Monoisotopic Mass
278.152 Da
Topological Polar Surface Area
52.600 Ų
Heavy Atom Count
20
Formal Charge
0
Complexity
271.000
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
The total count of all stereochemical bonds
0
Covalently-Bonded Unit Count
1
Citations of This Product
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