PRODUCTS

DIBUTYL SEBACATE(DBS)

CAS No.: 109-43-3
EC No.: 203-672-5

Dibutyl sebacate is used for plasticization: PVC, polyvinyl butyral, cellulose acetate, rubber. DBS gives products a high cold-resistance at low temperatures, light and water resistance.

Dibutyl sebacate is intended for plasticization of vinyl resins and other polymers in the production of the cable plasticates, artificial leather, industrial rubber products, polymeric building materials, linoleums, film and sheet materials, packaging films, PVC seals, gaskets for refrigerators, crown cork gaskets, and other purposes.

DIBUTYL SEBACATE

Dibutyl sebacate is used for plasticization: PVC, polyvinyl butyral, cellulose acetate, rubber. DBS gives products a high cold-resistance at low temperatures, light and water resistance.

Dibutyl sebacate is used for plasticization of paint and varnish materials on the base of cellulose esters and polyvinyl chloride. It provides coatings with a high frost-resistance.

Dibutyl sebacate is insoluble in water, soluble in organic solvents and hydrocarbons. It is used as plasticizer for vinyl polymers, particularly for polyvinyl chloride and vinyl chloride copolymers, as well as for cellulose nitrate, ethyl- and benzyl-cellulose. DBS is not toxic and can be used in products contacting with foodstuffs.

Dibutyl sebacate

Infobox references
Dibutyl sebacate (DBS) is an organic chemical, a dibutyl ester of sebacic acid. Its main use is as a plasticizer in production of plastics, namely cellulose acetate butyrate, cellulose acetate propionate, ethyl cellulose, polyvinyl butyral, polyvinyl chloride, polystyrene, and many synthetic rubbers (especially nitrile rubber and neoprene) and other plastics. It can be used for plastics in use in the food packaging industry, in plastics used for medical devices, and for pharmaceutical applications, e.g. as a plasticizer for film coating of tablets, beads, and granules.It is also used as a lubricant in shaving lotions, and a flavoring additive in non-alcoholic beverages, ice cream, ices, candy, and baked goods. It provides excellent compatibility[citation needed] with a range of plastic materials, superior properties at low temperatures, and good oil resistivity. Its other names include Morflex, Kodaflex, polycizer, Proviplast 1944 and PX 404. Dibutyl sebacate is also used as a desensitizer in Otto fuel II, a torpedo monopropellant.

Dibutyl sebacate's production and use as a plasticizer, rubber softener, flavoring agent and cosmetic and perfume additive may result in its release to the environment through its use and from various waste streams. If released to air, a vapor pressure of 4.7X10-6 mm Hg at 25 °C indicates dibutyl sebacate will exist in both the vapor and particulate phases in the ambient atmosphere. Vapor-phase dibutyl sebacate will be degraded in the atmosphere by reaction with photochemically-produced hydroxyl radicals; the half-life for this reaction in air is estimated to be 21 hours. Particulate-phase dibutyl sebacate will be removed from the atmosphere by wet and dry deposition. Dibutyl sebacate may also undergo direct photolysis since it contains a functional group that can absorb light greater than 290 nm, but the kinetics of this reaction are unknown. If released to soil, dibutyl sebacate is expected to have low mobility based upon an estimated Koc of 575. Volatilization from moist soil surfaces is not expected to be an important fate process based upon an estimated Henry's Law constant of 4.8X10-8 atm-cu m/mole. Volatilization from dry soil surfaces is not expected to be an important fate process based upon the vapor pressure. Dibutyl sebacate and other plasticizers were readily biodegraded by pure cultures. If released into water, dibutyl sebacate is expected to adsorb to suspended solids and sediment in water based upon the estimated Koc. Volatilization from water surfaces is not expected to be an important fate process based upon this compound's estimated Henry's Law constant. Hydrolysis is expected to occur slowly in the environment based on estimated hydrolysis half-lives of 166 days and 4.5 years at pH 8 and 7, respectively. An estimated BCF of 77 suggests the potential for bioconcentration in aquatic organisms is moderate. Occupational exposure to dibutyl sebacate may occur through inhalation and dermal contact with this compound at workplaces where dibutyl sebacate is produced or used. The general population is exposed to dibutyl sebacate through the use of consumer products that contain this compound. (SRC)

TERRESTRIAL FATE: Based on a classification scheme, an estimated Koc value of 575(SRC), determined from a water solubility of 40 mg/l and a regression-derived equation, indicates that dibutyl sebacate is expected to have low mobility in soil(SRC). Volatilization of dibutyl sebacate from moist soil surfaces is not expected to be an important fate process(SRC) given an estimated Henry's Law constant of 4.8X10-8 atm-cu m/mole(SRC), calculated from a vapor pressure of 4.7X10-6 mm Hg and water solubility of 40 mg/l. Dibutyl sebacate is not expected to volatilize from dry soil surfaces(SRC) based upon its vapor pressure. Dibutyl sebacate and other plasticizers were readily biodegraded by pure bacterial and fungal cultures.

AQUATIC FATE: Based on a classification scheme, an estimated Koc value of 575(SRC), determined from a water solubility of 40 mg/l and a regression-derived equation, indicates that dibutyl sebacate is expected to adsorb to suspended solids and sediment in water(SRC). Volatilization from water surfaces is not expected to be an important fate process based upon an estimated Henry's Law constant of 4.8X10-8 atm-cu m/mole(SRC), calculated from a vapor pressure of 4.7X10-6 mm Hg and water solubility of 40 mg/l. A base-catalyzed second-order hydrolysis rate constant of 0.05 L/mole-sec(SRC) was estimated using a structure estimation method; this corresponds to half-lives of 4.5 years and 166 days at pH values of 7 and 8, respectively. Dibutyl sebacate and other plasticizers were readily biodegraded by pure bacterial and fungal cultures. According to a classification scheme,an estimated BCF of 77(SRC), from its water solubility and a regression-derived equation, suggests the potential for bioconcentration in aquatic organisms is moderate(SRC).

ATMOSPHERIC FATE: According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere, dibutyl sebacate, which has a vapor pressure of 4.7X10-6 mm Hg at 25 °C, is expected to exist in both the vapor and particulate phases in the ambient atmosphere. Vapor-phase dibutyl sebacate is degraded in the atmosphere by reaction with photochemically-produced hydroxyl radicals(SRC); the half-life for this reaction in air is estimated to be 21 hours(SRC), calculated from its estimated rate constant of 1.8X10-11 cu cm/molecule-sec at 25 °C(SRC) determined using a structure estimation method. Particulate-phase dibutyl sebacate may be removed from the air by wet and dry deposition(SRC). Dibutyl sebacate may also undergo direct photolysis in the environment since this compound contains functional groups that can absorb light greater than 290 nm.

Dibutyl sebacate was degraded by pure bacterial and fungal cultures over 1 to 4 week incubation periods in shake flask experiments. Pure strains of the fungus Fusarium were shown to degrade dibutyl sebacate and several other plasticizers.

The rate constant for the vapor-phase reaction of dibutyl sebacate with photochemically-produced hydroxyl radicals has been estimated as 1.8X10-11 cu cm/molecule-sec at 25 °C(SRC) using a structure estimation method. This corresponds to an atmospheric half-life of about 21 hours at an atmospheric concentration of 5X10+5 hydroxyl radicals per cu cm. A base-catalyzed second-order hydrolysis rate constant of 0.05 L/mole-sec(SRC) was estimated using a structure estimation method; this corresponds to half-lives of 4.5 years and 166 days at pH values of 7 and 8, respectively. The expected hydrolysis products are butanol and sebacic acid. Dibutyl sebacate may also undergo direct photolysis in the environment since this compound contain a functional group that can absorb light greater than 290 nm.

The Henry's Law constant for dibutyl sebacate is estimated as 4.8X10-8 atm-cu m/mole(SRC) from its vapor pressure, 4.7X10-6 mm Hg, and water solubility, 40 mg/l. This Henry's Law constant indicates that dibutyl sebacate is expected to be essentially nonvolatile from water surfaces. Dibutyl sebacate's estimated Henry's Law constant indicates that volatilization from moist soil surfaces is not expected to be an important environmental fate process(SRC). Volatilization from dry soil surfaces is not expected to be an important fate process(SRC) based on the vapor pressure of this compound.

NIOSH (NOES Survey 1981-1983) has statistically estimated that 4,826 workers (2,128 of these are female) are potentially exposed to dibutyl sebacate in the US. Occupational exposure to dibutyl sebacate may occur through inhalation and dermal contact with this compound at workplaces where dibutyl sebacate is produced or used(SRC). The general population is exposed to dibutyl sebacate through the use of consumer products that contain this compound(SRC).

Dibutyl sebacate (DBS) is an organic chemical which is mainly used as a plasticizer in the production of such plastics as cellulose acetate butyrate, cellulose acetate propionate, ethyl cellulose, polyvinyl butyral, polyvinyl chloride, polystyrene, and many synthetic rubbers and other plastics. It is used for plastics in the food packaging industry, in medical devices, and for pharmaceutical applications. It is classified as mildly toxic by ingestion in humans and has shown experimental reproductive effects in animals; however, it is also approved by the US-FDA as a food additive to be used with the minimum quantity needed to produce the intended effect.

Dibutyl sebacate was selected as a plasticiser in the formulation of sustained-release matrix tablets. Dibutyl sebacate was added to a dichloromethane/EC solution and subsequently spray-dried, or was mixed as a liquid with EC powder. Hydrated tablets were evaluated by frequency sweep and creep rheological tests to correlate the results with drug release.
Route of Administration: Oral
In Vitro Use Guide
Dibutyl Sebacate (DBS) was diluted with dimethyl sulfoxide. Estrogenic activity was measured using a yeast two-hybrid system and a fluorescence polarization system within a concentration range of 10^-7 to 10^-3 M. Yeast strain Y190 was transformed with the pGBT9-receptors and pGAD424-coactivators using the lithium acetate method, and an S9 hepatic microsomal fraction was used to implement the mediating influence of metabolic bioactivation. DBS was tested for its ability to displaceflourescent non-steroid estrogen from the estrogen receptor. A threshold of B-galactosidase activity above 0.1, greater than 50% inhibition and a 1.5 fold increase in cell growth over controls was considered estrogenic activity. DBS showed the weakest cytotoxicity among tested compounds and an IC50 value for B-galactosidase that was higher than the applicable measurement range.

Chemical Properties
clear liquid
Chemical Properties
Dibutyl sebacate is a clear, colorless, oily liquid with a bland to slight butyl odor.
Uses
Dibutyl sebacate (DBS) is a dibutyl ester of sebacic acid. Dibutyl sebacate can be used for plastics in use in the food packaging industry, in plastics used for medical devices, and for pharmaceutical applications. Dibutyl sebacate is also used as a desensitizer in Otto fuel II, a torpedo monopropellant.
Production Methods
Dibutyl sebacate is manufactured by the esterification of n-butanol and sebacic acid in the presence of a suitable catalyst, and by the distillation of sebacic acid with n-butanol in the presence of concentrated acid.
Preparation
By distillation of sebacic acid with butyl alcohol in the presence of concentrated HCl in benzene solution or by reacting butyl alcohol and sebacyl chloride
Pharmaceutical Applications
Dibutyl sebacate is used in oral pharmaceutical formulations as a plasticizer for film coatings on tablets, beads, and granules, at concentrations of 10–30% by weight of polymer. It is also used as a plasticizer in controlled-release tablets and microcapsule preparations.
Dibutyl sebacate is also used as a synthetic flavor and flavor adjuvant in food products;for example,up to 5ppm is used in ice cream and nonalcoholic beverages.
Safety Profile
Mddly toxic by ingestion. Experimental reproductive effects. Combustible liquid when exposed to heat or flame; can react with oxidzing materials. To fight fire, use CO2 position it emits acrid smoke and fumes. See also ESTERS and n-BUTYL. ALCOHOL.
Safety
Dibutyl sebacate is used in cosmetics, foods, and oral pharmaceutical formulations, and is generally regarded as a nontoxic and nonirritant material. Following oral administration, dibutyl sebacate is metabolized in the same way as fats. In humans, direct eye contact and prolonged or repeated contact with the skin may cause very mild irritation. Acute animal toxicity tests and long-term animal feeding studies have shown no serious adverse effects to be associated with orally administered dibutyl sebacate.
LD50 (rat, oral): 16g/kg
storage
Dibutyl sebacate should be stored in a closed container in a cool, dry location. Dibutyl sebacate is stable under the recommended storage conditions and as used in specified applications under most conditions ofuse.Asanester,dibutylsebacatemayhydrolyzeinthe presence of water at high or low pH conditions.
Incompatibilities
Dibutyl sebacate is incompatible with strong oxidizing materials and strong alkalis.

Product Feature: Dibutyl Sebacate (DBS)

Dibutyl Sebacate DBS Chemical Structure
Dibutyl Sebacate (DBS), an ester of the castor-derived sebacic acid, is commonly used as a plasticizer in many different plastics including cellulose-based plastics, PVC, and synthetic rubber. In particular DBS is compatible with acrylics, cellulose acetate butyrate, cellulose acetate propionate, ethyl cellulose, polyvinyl butyral, polyvinyl chloride (PVC), polystyrene, nitrile rubber (NBR) and neoprene. DBS is approved for plastics used in the food packaging industry, plastics used for medical devices & tubing, as well as for pharmaceutical applications. DBS has good low temperature properties making it an excellent choice for food-contact films designed for refrigeration. DBS is used for lubricant applications, particularly in grease. In addition, DBS finds use in automotive, inks, personal care, and even flavoring applications. ChemCeed stocks this product in its traditional liquid form and also in a specially produced DBS powder form. Please inquire with us to receive a quote.

Di Butyl Sebacate (DBS)
Dibutyl sebacate (DBS) is an organic chemical, a dibutyl ester of sebacic acid. These sebacates plasticizers are used in production of plastics, namely cellulose acetate butyrate, cellulose acetate propionate, ethyl cellulose, polyvinyl butyral, polyvinyl chloride, polystyrene, and many synthetic rubbers (especially nitrile rubber and neoprene) and other plastics. It provides excellent compatibility with a range of plastic materials, superior properties at low temperatures, and good oil resistivit.

DIBUTYL SEBACATE
PRODUCT IDENTIFICATION
CAS NO.   109-43-3
DIBUTYL SEBACATE
EINECS NO.   203-672-5
FORMULA   [(CH2)4CO2(CH2)3CH3]2
MOL WT.   314.46
H.S. CODE
TOXICITY
Oral rat LD50: 14870 mg/kg
SYNONYMS   Sebacic acid, Dibutyl Ester;
Bis(N-butyl)Sebacate; Butyl Sebacate;
Decanedioic Acid, Dibutyl Ester; Di-n-butyl Sebacate; Dibutyl 1,8-octanedicarboxylate; Dibutyl Decanedioate; Dibutyl Sebacate; Dibutylester Kyseliny Sebakove;
RAW MATERIALS

CLASSIFICATION

PHYSICAL AND CHEMICAL PROPERTIES
PHYSICAL STATE   clear to faint yellow liquid
MELTING POINT   -10 C
BOILING POINT   178 - 179 C
SPECIFIC GRAVITY   0.94
SOLUBILITY IN WATER   Insoluble
SOLVENT SOLUBILITY
Soluble in hexane, toluene, ethanol and acetone. Insoluble in propylene glycol
pH
VAPOR DENSITY   10.8
HENRY'S LAW
NFPA RATINGS   Health: 0 Flammability: 1 Reactivity: 0
REFRACTIVE INDEX
FLASH POINT
167 C

STABILITY Stable under ordinary conditions
GENERAL DESCRIPTION AND APPLICATIONS

Dibutyl Sebacate is a plasticizer permitted in the field of food contact material, medical, and pharmaceutical. It is used as a plasticiser for polymers and synthetic rubbers.
There are almost infinite esters obtained from thousands of potential starting materials. Esters are formed by removal of water from an acid and an alcohol, e.g., carboxylic acid esters, phosphoric acid esters, and sulfonic acid esters. Carboxylic acid esters are used as in a variety of direct and indirect applications. Lower chain esters are used as flavouring base materials, plasticizers, solvent carriers and coupling agents. Higher chain compounds are used as components in metalworking fluids, surfactants, lubricants, detergents, oiling agents, emulsifiers, wetting agents textile treatments and emollients, They are also used as intermediates for the manufacture of a variety of target compounds. The almost infinite esters provide a wide range of viscosity, specific gravity, vapor pressure, boiling point, and other physical and chemical properties for the proper application selections.

Members of sebacic acid molecules
Product

CAS RN
1,1'-Isosebacoylbis(2-ethylaziridine)   25853-47-8
1,1'-Sebacoylbisaziridine   2798-06-3
1,4-Dioxatetradecane-5,14-dione   5578-82-5
1,6-Dioxacyclohexadecane-7,16-dione   58296-43-8
2,2,9,9-Tetramethylsebacic acid   22092-62-2
2-Ethylhexyl 2,2,5-trimethylhexyl sebacate   71607-40-4
2-Ethylhexyl nonyl sebacate   5137-28-0
2-Hydroxysebacic acid   103963-71-9
3,3'-(Sebacoyldiimino)bis(5-(acetamidomethyl)-2,4,6-triiodobenzoic acid)   25901-36-4
3,3'-(Sebacoyldiimino)bis(5-(propionamidomethyl)-2,4,6-triiodobenc acid)   25901-42-2
5,5'-Sebacoyldi(oxytryptamine) diacetate   52671-00-8
Ammonium hydrogen 9,10-dihydroxysebacate   84753-04-8
Ammonium octyl sebacate   4913-33-1
Barium sebacate   19856-32-7
Bis(2,2,6,6-tetramethyl-4-piperidinyl) sebacate   52829-07-9
Bis(2-ethoxyethyl) sebacate   624-10-2
Bis(2-methylbutyl) sebacate   93805-24-4
Bis(3,5-dibromosalicyl)sebacate   74134-05-7
Bis(3-methylbutyl) sebacate   10340-42-8
Bis(cholest-5-en-3beta-yl) sebacate   23394-16-3
Bis(tetrahydrofurfuryl) sebacate   4650-79-7
Butyl 2,3-dihydroxypropyl sebacate   94109-50-9
Cadmium sebacate   4476-04-4
Cerium(3+) sebacate   25418-94-4
Cerium(4+) sebacate   94232-56-1
Choline, chloride sebacate   28492-70-8
Cupric sebacate   58783-12-3
Decanedioic acid bis(1,2,2,6,6-pentamethyl-4-piperidinyl)ester   41556-26-7
Di-2-ethylhexyl sebacate   122-62-3
Di-2-ethylhexyl isosebacate   29590-28-1
Diallyl sebacate   3137-00-6
Dicyclohexyl sebacate   4121-15-7
Didocosyl sebacate   42233-75-0
Diethyl Sebacate   110-40-7
Diisodecyl sebacate   28473-19-0
Diisopropyl sebacate   7491-02-3
Dilithium sebacate   19370-86-6
Dimethyl hexadecafluorosebacate   4590-24-3
Di-n-butyl Sebacate   109-43-3
Di-n-decyl sebacate   2432-89-5
Di-n-dodecyl sebacate   2432-88-4
Di-n-hexadecyl sebacate   26719-48-2
Di-n-hexyl sebacate   2449-10-7
Di-n-octadecyl sebacate   3072-03-5
Di-n-octyl sebacate   2432-87-3
Di-n-tetradecyl sebacate   26719-47-1
Dipentyl sebacate   6819-09-6
Dipotassium sebacate   52457-55-3
Dipropyl sebacate   15419-91-7
Di-tert-butyl bisperoxysebacate   22537-96-8
Divinyl sebacate

10355-50-7
Docosyl hydrogen sebacate   93819-99-9
Dodecyl hydrogen sebacate   92739-54-3
Iosefamic acid   5591-33-3
Lanthanum(3+) sebacate   25418-93-3
Lithium hydrogen sebacate   94042-76-9
Lithium, 12-hydroxyoctadecanoate sebacate complex   68815-49-6
Lithium, dimethyl sebacate, 12-hydroxyoctadecanoate naphthenate complex   68919-36-8
Methyl hydrogen sebacate   818-88-2
Neodymium(3+) sebacate   25418-96-6
Perfluorosebacic acid   307-78-8
Polifeprosan 20   90409-78-2
Poly(ethylenesebacate)   25037-32-5
Poly(hexamethylene sebacate)   26745-88-0
Praseodymium(3+) sebacate   25418-95-5
Sebacic acid   111-20-6
Sebacic acid 1,3,5-triazine-2,4,6-triamine salt   31970-90-8
Sebacic acid 1,3,5-triazine-2,4,6-triamine salt   94159-18-9
Sebacic acid 2,2',2''-nitrilotriethanol complex   94202-16-1
Sebacic acid 2,2',2''-nitrilotriethanol complex   85030-06-4
Sebacic acid 2,2',2''-nitrilotriethanol complex   70103-35-4
Sebacic acid 2,2'-iminodiethanol complex   81189-11-9
Sebacic acid 2,2'-iminodiethanol complex   84145-30-2
Sebacic acid 2,2'-iminodiethanol complex   94200-21-2
Sebacic acid 2-aminoethanol complex   82801-62-5
Sebacic acid 2-butoxyethyl ester   68186-66-3
Sebacic acid bis(2-(2-butoxyethoxy)ethyl) ester   70900-46-8
Sebacic acid bis(2-butoxyethyl) ester   141-19-5
Sebacic acid bis(2-mercaptoethyl) ester   60642-69-5
Sebacic acid bis(2-methoxyethyl) ester   71850-03-8
Sebacic acid bis(phenylmethyl) ester   140-24-9
Sebacic acid dihydrazide   925-83-7
Sebacic acid diisooctyl ester   27214-90-0
Sebacic acid ditridecyl ester   2741-62-0
Sebacic acid morpholine complex   84522-37-2
Sebacic acid N-(2-aminoethyl)-N'-(2-((2-aminoethyl)amino)ethyl)ethane-1,2- diamine salt   84501-59-7
Sebacic acid 1,3,5-triazine-2,4,6-triamine salt   94159-19-0
Sebacic acid 1,6-hexanediamine salt   6422-99-7
Sebacic acid aluminum salt   5505-62-4
Sebacic acid bis((17beta-hydroxy-17-methylandrosta-1,4-dien-3-ylidene)hydrazide)   15437-53-3
Sebacic acid dimethyl ester   106-79-6
Sebacic acid dinonyl ester   4121-16-8
Sebacic acid disodium salt   17265-14-4
Sebacic acid lead(2+) salt   29473-77-6
Sebacic acid methyl 1,2,2,6,6-pentamethyl-4-piperidinyl ester   82919-37-7
Sebacic acid monoethyl ester   693-55-0
Sebacinyl-bis(1-methylpiperazine-4-methyl iodide)   61167-37-1
Sebacinyldicholine   7095-43-4
Sebacoyl chloride   111-19-3
Sebacoyldioxybis(tributylstannane)   30099-72-0
Sodium hydrogen sebacate   14047-57-5
Tetradecyl hydrogen sebacate   93819-98-8
Tetrahydrofurfuryl hydrogen sebacate   4650-83-3
SALES SPECIFICATION
APPEARANCE
Clear to yellow liquid
ESTER CONTENT
99.0% min
ACIDITY   0.03% max
SPECIFIC GRAVITY   0.934 - 0.940
WATER
0.05% max
HEAVY METALS
10ppm max
COLOR , APHA
50 max
TRANSPORTATION
PACKING   175kgs in drum
HAZARD CLASS   Not regulated
UN NO.
OTHER INFORMATION
Hazard Symbols: , Risk Phrases: Safety Phrases: 24/25-28A-37-45
GENERAL DESCRIPTION OF DICARBOXYLIC ACID
Dicarboxylic acid is a compound containing two carboxylic acid, -COOH, groups. Examples are shown in table. In substitutive nomenclature their names are formed by adding -dioic' as a suffix to the name of the parent compound. They can yield two kinds of salts, as they contain two carboxyl groups in its molecules.

Dibutyl sebacate is used for plasticization: PVC, polyvinyl butyral, cellulose acetate, rubber. DBS gives products a high cold-resistance at low temperatures, light and water resistance.

Dibutyl sebacate is used for plasticization of paint and varnish materials on the base of cellulose esters and polyvinyl chloride. It provides coatings with a high frost-resistance.

Synonyms:
DIBUTYL SEBACATE; Dibutyl sebacate; DİBÜTİL SEBAKAT; dibütil sebakat; DIBUTYL SEBACATE; Dibutyl decanedioate; 109-43-3; Butyl sebacate; Di-n-butyl sebacate; Decanedioic acid, dibutyl ester; Polycizer DBS; Kodaflex DBS; Dibutyl sebacinate; Staflex DBS; Monoplex DBS; Bis(n-butyl) sebacate; Sebacic acid, dibutyl ester; Di-n-butylsebacate; Bis(n-butyl)sebacate; 1,10-dibutyl decanedioate; Dibutylester kyseliny sebakove; Di(n-butyl) sebacate; PX 404; Decanedioic Acid Dibutyl Ester; Dibutyl 1,8-octanedicarboxylate; UNII-4W5IH7FLNY; n-Butyl sebacate; Plasthall DBS; Sebacic acid dibutyl ester; Uniflex DBS; NSC 3893; DIBUTYL SEBACATE; Dibutyl sebacate; DİBÜTİL SEBAKAT; dibütil sebakat; DIBUTYL SEBACATE; Dibutyl sebacate; DİBÜTİL SEBAKAT; dibütil sebakat; Reomol DBS; Decanedioic acid, 1,10-dibutyl ester; Dibutyl sebacate (NF); Dibutyl sebacate [NF]; MFCD00027218; 4W5IH7FLNY; Dibutyl sebacate, 93%; DSSTox_CID_21847; DSSTox_RID_79856; DSSTox_GSID_41847; CAS-109-43-3; Di-n-butyl-sebacate; DIBUTYL SEBACATE; Dibutyl sebacate; DİBÜTİL SEBAKAT; dibütil sebakat; DIBUTYL SEBACATE; Dibutyl sebacate; DİBÜTİL SEBAKAT; dibütil sebakat; FEMA No. 2373; HSDB 309; Di-n-butyl decanedioate; EINECS 203-672-5; Dibutylester kyseliny sebakove [Czech]; BRN 1798308; AI3-00393; CCRIS 8264; di-butyl sebacate; ACMC-1BUY3; EC 203-672-5; Dibutyl sebacate, >=90%; Di-n-butyl sebacate, 90%; SCHEMBL42655; 4-02-00-02081 (Beilstein Handbook Reference); KSC175Q6R; CHEMBL2106225; DTXSID1041847; CTK0H5868; FEMA 2373; Sebacic acid, bis-n-butyl ester; DIBUTYL SEBACATE; Dibutyl sebacate; DİBÜTİL SEBAKAT; dibütil sebakat; DIBUTYL SEBACATE; Dibutyl sebacate; DİBÜTİL SEBAKAT; dibütil sebakat; Dibutyl sebacate, technical grade; NSC3893; CHEBI:165632; KS-00000YU3; NSC-3893; ZINC3875764; Tox21_113651; Tox21_300154; ANW-16045; Dibutyl sebacate, analytical standard; LMFA07010828; s6041; Dibutyl sebacate, >=97.0% (GC); AKOS015915581; CS-W014523; HY-W013807; NCGC00247910-01; NCGC00247910-02; NCGC00254088-01; BS-14305; I839; DB-040869; FT-0624681; D03782; Dibutyl sebacate, SAJ first grade, >=98.0%; Dibutyl sebacate, Selectophore(TM), >=97.0%; DIBUTYL SEBACATE; Dibutyl sebacate; DİBÜTİL SEBAKAT; dibütil sebakat; Q411272; SR-01000944769; J-002279; J-520240; SR-01000944769-1; Dibutyl sebacate, United States Pharmacopeia (USP) Reference Standard; Dibutyl sebacate, Pharmaceutical Secondary Standard; Certified Reference Material; butyl sebacate; bis(N-butyl) sebacate; bis(N-butyl)sebacate; decane dioic acid dibutyl ester; decanedioic acid dibutyl ester; decanedioic acid, dibutyl ester; DIBUTYL SEBACATE; Dibutyl sebacate; DİBÜTİL SEBAKAT; dibütil sebakat; DIBUTYL SEBACATE; Dibutyl sebacate; DİBÜTİL SEBAKAT; dibütil sebakat; di-N-butyl decanedioate; di-N-butyl sebacate; di-N-butyl-sebacate; dibutyl 1,8-octane dicarboxylate; dibutyl 1,8-octanedicarboxylate; dibutyl decane dioate; dibutyl decane-1,10-dioate, dibutyl decanedioate; 1,10-dibutyl decanedioate; dibutyl sebacate, tech.; dibutylsebacate; kodaflex DBS; DIBUTYL SEBACATE; Dibutyl sebacate; DİBÜTİL SEBAKAT; dibütil sebakat; monoplex DBS; polycizer DBS; sebacic acid di-N-butyl ester; sebacic acid dibutyl ester; sebacic acid, dibutyl ester; staflex DBS; BUTYL SEBACATE; DIBUTYL DECANEDIOATE; DIBUTYL 1,8-OCTANEDICARBOXYLATE; SEBACIC ACID DIBUTYL ESTER; DIBUTYL SEBACATE; Dibutyl sebacate; DİBÜTİL SEBAKAT; dibütil sebakat; RUBIN; px404; ROSEIN; PX 404; MAGENTA; NSC 3893; CL 42500; ReoMol D; MAGENTA O; ROSANILIN; DIBUTYL SEBACATE; Dibutyl sebacate; DİBÜTİL SEBAKAT; dibütil sebakat; DIBUTYL SEBACATE; Dibutyl sebacate; DİBÜTİL SEBAKAT; dibütil sebakat; DIBUTYL SEBACATE; Dibutyl decanedioate; 109-43-3; Butyl sebacate; Di-n-butyl sebacate; Decanedioic acid, dibutyl ester; Polycizer DBS; Kodaflex DBS; Dibutyl sebacinate; Staflex DBS; Monoplex DBS; Bis(n-butyl) sebacate; Sebacic acid, dibutyl ester; Di-n-butylsebacate; Bis(n-butyl)sebacate; 1,10-dibutyl decanedioate; Dibutylester kyseliny sebakove; Di(n-butyl) sebacate; PX 404; Decanedioic Acid Dibutyl Ester; Dibutyl 1,8-octanedicarboxylate; UNII-4W5IH7FLNY; n-Butyl sebacate; Plasthall DBS; Sebacic acid dibutyl ester; Uniflex DBS; NSC 3893; DIBUTYL SEBACATE; Dibutyl sebacate; DİBÜTİL SEBAKAT; dibütil sebakat; DIBUTYL SEBACATE; Dibutyl sebacate; DİBÜTİL SEBAKAT; dibütil sebakat; Reomol DBS; Decanedioic acid, 1,10-dibutyl ester; Dibutyl sebacate (NF); Dibutyl sebacate [NF]; MFCD00027218; 4W5IH7FLNY; Dibutyl sebacate, 93%; DSSTox_CID_21847; DSSTox_RID_79856; DSSTox_GSID_41847; CAS-109-43-3; Di-n-butyl-sebacate; DIBUTYL SEBACATE; Dibutyl sebacate; DİBÜTİL SEBAKAT; dibütil sebakat; DIBUTYL SEBACATE; Dibutyl sebacate; DİBÜTİL SEBAKAT; dibütil sebakat; FEMA No. 2373; HSDB 309; Di-n-butyl decanedioate; EINECS 203-672-5; Dibutylester kyseliny sebakove [Czech]; BRN 1798308; AI3-00393; CCRIS 8264; di-butyl sebacate; ACMC-1BUY3; EC 203-672-5; Dibutyl sebacate, >=90%; Di-n-butyl sebacate, 90%; SCHEMBL42655; 4-02-00-02081 (Beilstein Handbook Reference); KSC175Q6R; CHEMBL2106225; DTXSID1041847; CTK0H5868; FEMA 2373; Sebacic acid, bis-n-butyl ester; DIBUTYL SEBACATE; Dibutyl sebacate; DİBÜTİL SEBAKAT; dibütil sebakat; DIBUTYL SEBACATE; Dibutyl sebacate; DİBÜTİL SEBAKAT; dibütil sebakat; Dibutyl sebacate, technical grade; NSC3893; CHEBI:165632; KS-00000YU3; NSC-3893; ZINC3875764; Tox21_113651; Tox21_300154; ANW-16045; Dibutyl sebacate, analytical standard; LMFA07010828; s6041; Dibutyl sebacate, >=97.0% (GC); AKOS015915581; CS-W014523; HY-W013807; NCGC00247910-01; NCGC00247910-02; NCGC00254088-01; BS-14305; I839; DB-040869; FT-0624681; D03782; Dibutyl sebacate, SAJ first grade, >=98.0%; Dibutyl sebacate, Selectophore(TM), >=97.0%; DIBUTYL SEBACATE; Dibutyl sebacate; DİBÜTİL SEBAKAT; dibütil sebakat; Q411272; SR-01000944769; J-002279; J-520240; SR-01000944769-1; Dibutyl sebacate, United States Pharmacopeia (USP) Reference Standard; Dibutyl sebacate, Pharmaceutical Secondary Standard; Certified Reference Material; butyl sebacate; bis(N-butyl) sebacate; bis(N-butyl)sebacate; decane dioic acid dibutyl ester; decanedioic acid dibutyl ester; decanedioic acid, dibutyl ester; DIBUTYL SEBACATE; Dibutyl sebacate; DİBÜTİL SEBAKAT; dibütil sebakat; DIBUTYL SEBACATE; Dibutyl sebacate; DİBÜTİL SEBAKAT; dibütil sebakat; di-N-butyl decanedioate; di-N-butyl sebacate; di-N-butyl-sebacate; dibutyl 1,8-octane dicarboxylate; dibutyl 1,8-octanedicarboxylate; dibutyl decane dioate; dibutyl decane-1,10-dioate, dibutyl decanedioate; 1,10-dibutyl decanedioate; dibutyl sebacate, tech.; dibutylsebacate; kodaflex DBS; DIBUTYL SEBACATE; Dibutyl sebacate; DİBÜTİL SEBAKAT; dibütil sebakat; monoplex DBS; polycizer DBS; sebacic acid di-N-butyl ester; sebacic acid dibutyl ester; sebacic acid, dibutyl ester; staflex DBS; BUTYL SEBACATE; DIBUTYL DECANEDIOATE; DIBUTYL 1,8-OCTANEDICARBOXYLATE; SEBACIC ACID DIBUTYL ESTER; DIBUTYL SEBACATE; Dibutyl sebacate; DİBÜTİL SEBAKAT; dibütil sebakat; RUBIN; px404; ROSEIN; PX 404; MAGENTA; NSC 3893; CL 42500; ReoMol D; MAGENTA O; ROSANILIN; DIBUTYL SEBACATE; Dibutyl sebacate; DİBÜTİL SEBAKAT; dibütil sebakat