Butynorate = Dibutyltin dilaurate
CAS Number: 77-58-7
EC Number: 201-039-8
Molecular Weight: 631.56
Chemical formula: C32H64O4Sn
Butynorate (abbreviated DBTDL), also called dibutyltindilaurate or Dibutyltin dilaurate, is an organotin compound that is used as a catalyst.
Butynorate is a colourless oily liquid.
In terms of Butynorate structure, the molecule consists of two laurate groups attached to a dibutyltin(IV) center.
The molecular geometry at tin is tetrahedral.
Based on the crystal structure of the related bis(bromobenzoate), the carbonyl oxygen centers are weakly bonded to tin.
Together with dibutyltin dioctanoate, Butynorate is used as a catalyst for polyurethane production from isocyanates and diols.
Butynorate is also useful as a catalyst for transesterification and for the room temperature vulcanization of silicones.
Butynorate is also used as a stabilizer in polyvinyl chloride.
Butynorate is also added to animal feed to remove cecal worms, roundworms, and tapeworms in turkeys to prevent hexamitosis and coccidiosis.
Butynorate is a light yellow or colorless oily liquid, low temperature into a white crystalline powder.
Soluble in benzene, toluene, ethyl acetate, ethanol, acetone, chloroform, carbon tetrachloride, petroleum ether, in most common solvents and various industrial plasticizer, insoluble in water.
Butynorate is a catalyst for solvent-based two-component polyurethane systems.
This solution is suitable for accelerating cross-linking processes.
Butynorate improves the drying of chemically curing systems favoring the isocyanate/polyol reaction over other side reactions such as isocyanate/water.
Butynorate enhances scratch resistance, hardness, and mechanical properties.
This catalyst can be used to aid the curing process of polyurethanes, silicone resins, RTV silicone resins, and silane modified polymers.
Butynorate is an organotin compound that is usually abbreviated to DBTL or DBTDL.
The colorless to yellowish liquid has an oily consistency, is extremely flammable and gives off a fatty acid-like smell.
Butynorate is soluble in acetone, methanol or other organic solvents, but is practically insoluble in water.
Butynorate catalyzes esterification reactions, transesterification reactions and polycondensation reactions and has become the industry standard for coatings, adhesives, solvents and elastomers.
Butynorate is a universally applicable catalyst for the crosslinking of cold vulcanizing silicone rubbers and silane-modified polymers and is widely used.
From “construction market” silicone for sealing tiles at home to industrial applications such as in the production of cables, cast resin systems or RTV sealants used in the automotive industry.
Two modes of action are possible: the DBTL catalyst supports the curing of room temperature crosslinking silicone rubbers.
Exposed to the air, the ambient humidity reacts with the tin compound and the silicone mass solidifies.
Butynorate accelerates this reaction and provides better processing properties.
Alternatively used two-component silicones harden not only by contact with the humidity, but require a second reaction partner to be supplied.
Another application of Butynorate is the production of polyurethanes for a wide variety of end applications.
Hard foams, sealants, adhesives, paints and coatings or large floors, As an additive, DBTL accelerates the connection of the individual reaction partners in order to reduce the curing time.
For example, Butynorate is a common crosslinking catalyst that can be used for 2-component urethanes in the automotive industry or for other industrial applications, such as the coating of tanks, pipelines or floor coverings.
On silica adsorbed, DBTL is used in urethane-based powder coatings for areas that have to withstand high weather loads.
Soft and solid PU foams are a standard solution for plastic molded parts that have to withstand loads in everyday life, such as seats or cladding.
Butynorate is also a widely used gelling catalyst.
The application possibilities also include elastomers.
Butynorate (DBTDL) is an organotin compound that is used as a catalyst for polyurethane production from isocyanates and diols.
Butynorate improves the drying of chemically curing systems favoring the isocyanate/polyol reaction over other side reactions such as isocyanate/water.
Butynorate can be used to aid the curing process of polyurethanes, silicone resins, RTV silicone resins and silane modified polymers.
Butynorate was used for the removal of large roundworms, cecal worms, and several species of tapeworms from chickens and turkeys.
Based on animal studies, prolonged or repeated overexposure to Butynorate may affect the developing fetus, blood, and thymus.
Overexposure to Butynorate may also cause central nervous system effects.
Butynorate is a yellow liquid which has C32H64O4Sn as chemical formula.
Butynorate is used in the production of polyether and polyester based polyurethanes.
Further Butynorate finds Butynorate application as catalyst in both adhesives and sealants.
Other uses include heat stabilizer for PVC and room temperature vulcanization (RTV) of sillicone polymers.
Butynorate is also known as di-n-butyldilauryltin, dibutylbis(lauroyloxy)stannane and dibutyltin didodecanoate.
Butynorate is an organic tin additives, and can be soluble in benzene, toluene, carbon tetrachloride, ethyl acetate, chloroform, acetone, petroleum ether and other organic solvents and all industrial plasticizers, but insoluble in water.
Multipurpose high-boiling organic tin catalyst circulation of Butynorate are usually specially treated liquefaction, and at room temperature as a pale yellow or colorless oily liquid, when low temperature as white crystals, and Butynorate can be used for PVC additives, Butynorate also has excellent lubricity, transparency, weather resistance, and better resistance for sulfide pollution.
Butynorate can also uesd the stabilizer of the soft transparent products and efficient lubricants in hard transparent products, and can also be used acrylate rubber and rubber carboxyl crosslinking reaction, the catalyst of synthesis of polyurethane foam and polyester synthetic, and RTV silicone rubber.
Butynorate is registered under the REACH Regulation and is manufactured in and / or imported to the European Economic Area, at ≥ 100 to < 1 000 tonnes per annum.
Butynorate is used by consumers, in articles, by professional workers (widespread uses), in formulation or re-packing, at industrial sites and in manufacturing.
Physical Description of Butynorate:
Butynorate is a clear yellow viscous liquid.
Soft solid or yellow liquid
mp = 22-24 deg C
Yellow oily liquid or waxy solid
Yellow viscous liquid
Butynorate, also called dibutyltindilaurate or Dibutyltin dilaurate, is an organotin compound that is used as a catalyst.
KEYWORDS:
77-58-7, 201-039-8, Dibutyltin dilaurate, DBTDL, Stavinor 1200 SN, Ongrostab BLTM, Dibutylbis(lauroyloxy)tin, Thermolite T 12, Bis(lauroyloxy)di(n-butyl)stannane, Kosmos 19
Chemical properties of Butynorate:
Butynorate is pale yellow flammable liquid, and soluble in acetone and benzene, can not dissolve in water.
Features of Butynorate:
Suitable to accelerate the cross-linking process of solvent-based two-component PU coatings
Improves the drying of chemically curing systems favoring the isocyanate/polyol reaction over other side reactions such as isocyanate/water
Enhances scratch resistance, hardness, and mechanical properties
Can be used to aid the curing process of polyurethanes, silicone resins, RTV silicone resins, and silane modified polymers
Applications of Butynorate:
Butynorate has been used as a catalyst in a protocol for the covalent attachment of poly(ethylene glycol) (PEG) to silicon oxide to form a hydrophilic non-fouling surface.
Butynorate can also be used as a catalyst in the preparation of polymers by reacting hydroxyl-terminated macromonomers and aliphatic diisocyanates.
Catalyst in the production of polyurethane and curing of room temperature vulcanising silicon rubber.
Butynorate also finds application as catalyst in the manufacture of silane-crosslinking polyolefins.
Butynorate is also used in heat stabilisers in PVC.
Ideal applications for Butynorate include solvent-based, chemical cross-linking, two-component polyurethane systems.
Butynorate has been used as a catalyst in a protocol for the covalent attachment of poly(ethylene glycol) (PEG) to silicon oxide to form a hydrophilic non-fouling surface.
Butynorate can also be used as a catalyst in the preparation of polymers by reacting hydroxyl-terminated macromonomers and aliphatic diisocyanates.
PVC stabilizer products and lubricants soft PVC transparent products or semi soft products, with stearic acid barium, cadmium stearic acid and other metal soap or epoxy compound and has good lubricity, transparency, weather resistance, and plasticizer compatibility, spray cream, no curing pollution, on the heat resistance and printing without adverse effects.
Such as: soft film, film, plastic shoes, PVC hose and conveyor belt.
Especially can be used as catalyst for polyurethane foam products.
In rigid PVC products, this product can be used as, and maleic acid
Organic tin or thiol organic tin and use, improve resin fluidity.
The polyurethane foam plastic, PVC foam, silicon rubber composite material is used as a catalyst and foaming activator.
A variety of adhesives used in synthesis catalyst.
Solvent-based, chemical cross-linking, two-component coating
Polyurethane systems
Other Applications of Butynorate:
The catalytic effect of the Butynorate is used in other areas, such as acrylic acid esters, the production of silica esters or alkyd resins.
For screen printing processes, print shop chemicals with DBTL content can be used.
As PVC Stabilizer:
Butynorate is only through the use of stabilizers that PVC plastics are given a durability with which they can be used economically.
Butynorate has such stabilizing properties and protects the final product from heat and UV irradiation.
Product Variants:
BNT offers Butynorate in various product variants, specifically geared to individual requirement profiles.
Butynorate from BNT is a PVC stabilizer and universal catalyst, for example a catalysis in the production of silicone rubbers and polyurethanes, as a binder for alkyd resins or additive in polymer processing.
In addition to the catalytic properties, BNT-CAT 420 and BNT-CAT 423 have a particularly light-stabilizing effect.
BNT-CAT 422, on the other hand, is particularly heat-stabilizing.
Intended Use of Butynorate:
Used as a catalyst in soft and semi-soft materials.
Used as a stabilizer (polyvinyl chloride resins, vinyl resins, lacquers, and elastomers), a catalyst for urethane and silicones, and a drug (anthelmintic and coccidiostat).
Industrial Processes with risk of exposure:
Painting (Pigments, Binders, and Biocides)
Stabilizer for polyvinyl chloride resins.
Catalyst for curing certain silicones.
Stabilizer for vinyl resins, lacquers, elastomers; catalyst for urethane and silicones.
In the United States, dibutyltin compounds are used mostly in the catalysis of rigid foams and the laurate has been the catalyst of choice.
Catalyst for the curing of room-temperature-vulcanized (RTV) silicone elastomers to produce flexible silicone rubbers used as sealing compounds, insulators, and in a wide variety of other applications.
Plastics - Typical concentration range in plastic materials -> 3%
Uses of Butynorate:
Butynorate can be used as PVC heat stabilizers, and Butynorate is the earliest used varieties in organotin stabilizers, heat resistance is less than tributyltin maleate, but Butynorate has excellent lubricity, weather resistance and transparency can be ok, and Butynorate has good compatibility with plasticizers, non-blooming, non-sulfide pollution, no adverse effects on heat sealing and printability.
For Butynorate is liquid at room temperature, so the dispersion in plastic is better than solid stabilizer.
Butynorate is mainly used in soft transparent products or semi-soft products, generally in an amount of 1-2%.
In hard products, the product can be used as lubricant, and when used with maleic acid organic tin or thiol-containing organic tin can improve the fluidity of the resin material.
Compared with other organic tin, the goods early color large will cause yellow discoloration.
Butynorate can also be used as catalysts of synthesizing polyurethane, the curing agents of silicone rubber.
In order to enhance the thermal stability, transparency, compatibility with resins, as well as improve the impact strength for hard products and Butynorate other properties, now Butynorate has developed a number of modified varieties.
Lauric acid and other fatty acids is generally added in the category of pure, the epoxy ester or other metal soap stabilizer is also added in.
Butynorate is toxic materials.
Uses of Butynorate:
Furniture and furnishing
Home maintenance
Home maintenance - caulk/sealant
Catalyst
Heat stabilizers
Home maintenance - paint/stain and related products
Home maintenance - paint/stain and related products - paint
Home maintenance - surface sealers
Pet care - cats
Primer ingredient
Industry Uses of Butynorate:
Butynorate is used in the following products: polymers, adhesives and sealants, coating products, paper chemicals and dyes, textile treatment products and dyes, metal surface treatment products, non-metal-surface treatment products, polishes and waxes and washing & cleaning products.
Butynorate has an industrial use resulting in manufacture of another substance (use of intermediates).
Butynorate is used in the following areas: building & construction work and formulation of mixtures and/or re-packaging.
Butynorate is used for the manufacture of: chemicals, plastic products, electrical, electronic and optical equipment, machinery and vehicles, textile, leather or fur, wood and wood products, pulp, paper and paper products, rubber products, fabricated metal products and furniture.
Release to the environment of Butynorate can occur from industrial use: in the production of articles, as processing aid, in processing aids at industrial sites, as processing aid and formulation in materials.
Butynorate is used as:
Adhesives and sealant chemicals,
Catalyst,
Heat Stabilizers,
Paint additives and coating additives not described by other categories,
Process regulators,
Processing aids, not otherwise listed,
Catalyst.
Consumer Uses of Butynorate:
Butynorate is used in the following products: adhesives and sealants and coating products.
Other release to the environment of Butynorate is likely to occur from: indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners), outdoor use, outdoor use in long-life materials with low release rate (e.g. metal, wooden and plastic construction and building materials) and indoor use in long-life materials with low release rate (e.g. flooring, furniture, toys, construction materials, curtains, foot-wear, leather products, paper and cardboard products, electronic equipment).
Butynorate is used as:
Adhesives and sealants
Building/construction materials not covered elsewhere
Paints and coatings
Plastic and rubber products not covered elsewhere
Urethanes
Widespread uses by professional workers of Butynorate:
Butynorate is used in the following products: adhesives and sealants, coating products and fillers, putties, plasters, modelling clay.
Butynorate is used in the following areas: building & construction work.
Other release to the environment of Butynorate is likely to occur from: indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners) and outdoor use.
Manufacture of Butynorate:
Release to the environment of Butynorate can occur from industrial use: manufacturing of the substance.
General Manufacturing Information of Butynorate:
Industry Processing Sectors:
Adhesive manufacturing
Construction
Electrical equipment, appliance, and component manufacturing
Miscellaneous manufacturing
Paint and coating manufacturing
Plastic material and resin manufacturing
Plastics product manufacturing
Transportation equipment manufacturing
urethane
Pharmacology and Biochemistry of Butynorate:
Mechanism of Action:
Rats fed Butynorate at a dose of 17.5 mg/kg per day for 15 days by oral intubation exhibited a 15% stimulation of heme oxygenase activity and a decreased hepatocellular cytochrome p450 content.
These effects were accompanied by a decrease in the specific activities of several microsomal enzymes.
In addition, pentobarbital-induced sleeping time was increased in proportion to the duration of the dibutyltin exposure, demonstrating the impairment of barbiturate metabolism in the dibutyltin-treated animals.
Drug and Medication Information of Butynorate:
Therapeutic Uses of Butynorate:
Anthelmintics
Coccidiostats
MEDICATION (VET): Butynorate (Polystat, Tinostat) is added to feed to remove cecal worms, roundworms, & tapeworms in turkeys to prevent hexamitosis & coccidiosis.
The dose ranges between 200 & 1400 ppm.
Handling and Storage of Butynorate:
Nonfire Spill Response:
SMALL SPILLS AND LEAKAGE: If you spill this chemical, use absorbent paper to pick up all liquid spill material.
Your contaminated clothing and absorbent paper should be sealed in a vapor-tight plastic bag for eventual disposal.
Solvent wash all contaminated surfaces with alcohol followed by washing with a strong soap and water solution.
Do not reenter the contaminated area until the Safety Officer (or other responsible person) has verified that the area has been properly cleaned.
STORAGE PRECAUTIONS:
You should store this material in a refrigerator.
Storage of Butynorate:
Store in an area without drain or sewer access.
Keep containers tightly closed in a dry, cool and well-ventilated place.
Keep away from sources of ignition.
Store Butynorate in original container.
Store Butynorate in accordance with local regulations.
Keep at temperatures between 5 °C and 30 °C.
Formulation or re-packing of Butynorate:
Butynorate is used in the following products: polymers, adhesives and sealants, coating products, paper chemicals and dyes, textile treatment products and dyes, metal surface treatment products, non-metal-surface treatment products, polishes and waxes and washing & cleaning products.
Butynorate has an industrial use resulting in manufacture of another substance (use of intermediates).
Release to the environment of Butynorate can occur from industrial use: formulation of mixtures, formulation in materials, in processing aids at industrial sites, in the production of articles, as processing aid and as processing aid.
Stability/Shelf Life of Butynorate:
Butynorate lacks any great stability at high temperatures.
Safety Information of Butynorate:
Signal Word: Danger
Target Organs: thymus
Storage Class Code: 6.1C - Combustible, acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK: WGK 3
Flash Point(F): 372.2 - 379.4 °F - closed cup
Flash Point(C): 189 - 193 °C - closed cup
Personal Protective Equipment: dust mask type N95 (US), Eyeshields, Gloves
Reactivity Profile of Butynorate:
Butynorate is strongly reactive with many other groups.
Incompatible with acids and bases.
Organometallics are good reducing agents and therefore incompatible with oxidizing agents.
First Aid of Butynorate:
EYES: First check the victim for contact lenses and remove if present.
Flush victim's eyes with water or normal saline solution for 20 to 30 minutes while simultaneously calling a hospital or poison control center.
Do not put any ointments, oils, or medication in the victim's eyes without specific instructions from a physician.
IMMEDIATELY transport the victim after flushing eyes to a hospital even if no symptoms (such as redness or irritation) develop.
SKIN: IMMEDIATELY flood affected skin with water while removing and isolating all contaminated clothing.
Gently wash all affected skin areas thoroughly with soap and water.
If symptoms such as redness or irritation develop, IMMEDIATELY call a physician and be prepared to transport the victim to a hospital for treatment.
INHALATION: IMMEDIATELY leave the contaminated area; take deep breaths of fresh air.
If symptoms (such as wheezing, coughing, shortness of breath, or burning in the mouth, throat, or chest) develop, call a physician and be prepared to transport the victim to a hospital.
Provide proper respiratory protection to rescuers entering an unknown atmosphere.
Whenever possible, Self-Contained Breathing Apparatus (SCBA) should be used; if not available, use a level of protection greater than or equal to that advised under Protective Clothing.
INGESTION: Some heavy metals are VERY TOXIC POISONS, especially if their salts are very soluble in water (e.g., lead, chromium, mercury, bismuth, osmium, and arsenic).
IMMEDIATELY call a hospital or poison control center and locate activated charcoal, egg whites, or milk in case the medical advisor recommends administering one of them.
Also locate Ipecac syrup or a glass of salt water in case the medical advisor recommends inducing vomiting.
Usually, this is NOT RECOMMENDED outside of a physician's care.
If advice from a physician is not readily available and the victim is conscious and not convulsing, give the victim a glass of activated charcoal slurry in water or, if this is not available, a glass of milk, or beaten egg whites and IMMEDIATELY transport victim to a hospital.
If the victim is convulsing or unconscious, do not give anything by mouth, assure that the victim's airway is open and lay the victim on his/her side with the head lower than the body.
DO NOT INDUCE VOMITING.
IMMEDIATELY transport the victim to a hospital.
Fire Fighting of Butynorate:
Fires involving this compound should be controlled using a dry chemical, carbon dioxide or Halon extinguisher.
Accidental Release Measures of Butynorate:
Isolation and Evacuation
As an immediate precautionary measure, isolate spill or leak area in all directions for at least 50 meters (150 feet) for liquids and at least 25 meters (75 feet) for solids.
SPILL: Increase, in the downwind direction, as necessary, the isolation distance shown above.
FIRE: If tank, rail car or tank truck is involved in a fire, ISOLATE for 800 meters (1/2 mile) in all directions; also, consider initial evacuation for 800 meters (1/2 mile) in all directions. (ERG, 2016)
Spillage Disposal of Butynorate:
Personal protection: particulate filter respirator adapted to the airborne concentration of the substance.
Collect leaking and spilled liquid in sealable containers as far as possible.
Sweep spilled substance into covered containers.
If appropriate, moisten first to prevent dusting.
Carefully collect remainder.
Then store and dispose of according to local regulations.
Do NOT let this chemical enter the environment.
Disposal Methods of Butynorate:
At the time of review, criteria for land treatment or burial (sanitary landfill) disposal practices are subject to significant revision.
Prior to implementing land disposal of waste residue (including waste sludge), consult with environmental regulatory agencies for guidance on acceptable disposal practices.
Preventive Measures of Butynorate:
Avoid the vapor produced by heating.
The scientific literature for the use of contact lenses in industry is conflicting.
The benefit or detrimental effects of wearing contact lenses depend not only upon the substance, but also on factors including the form of the substance, characteristics and duration of the exposure, the uses of other eye protection equipment, and the hygiene of the lenses.
However, there may be individual substances whose irritating or corrosive properties are such that the wearing of contact lenses would be harmful to the eye.
In those specific cases, contact lenses should not be worn.
In any event, the usual eye protection equipment should be worn even when contact lenses are in place.
Release to the environment of Butynorate can occur from industrial use: as processing aid, formulation in materials, in processing aids at industrial sites, in the production of articles and as processing aid.
Other release to the environment of Butynorate is likely to occur from: indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners), outdoor use, outdoor use in long-life materials with low release rate (e.g. metal, wooden and plastic construction and building materials) and indoor use in long-life materials with low release rate (e.g. flooring, furniture, toys, construction materials, curtains, foot-wear, leather products, paper and cardboard products, electronic equipment).
Butynorate can be found in complex articles, with no release intended: vehicles, machinery, mechanical appliances and electrical/electronic products (e.g. computers, cameras, lamps, refrigerators, washing machines) and electrical batteries and accumulators.
Butynorate can be found in products with material based on: fabrics, textiles and apparel (e.g. clothing, mattress, curtains or carpets, textile toys), leather (e.g. gloves, shoes, purses, furniture), rubber (e.g. tyres, shoes, toys) and wood (e.g. floors, furniture, toys).
Identifiers of Butynorate:
CAS Number: 77-58-7
ChemSpider: 21106564
ECHA InfoCard: 100.000.946
EC Number: 201-039-8
PubChem CID: 16682738
RTECS number: WH7000000
UNII: L4061GMT90
UN number: 3146
CompTox Dashboard (EPA): DTXSID6024961
InChI: InChI=1S/2C12H24O2.2C4H9.Sn/c2*1-2-3-4-5-6-7-8-9-10-11-12(13)14;2*1-3-4-2;/h2*2-11H2,1H3,(H,13,14);2*1,3-4H2,2H3;/q;;;;+2/p-2
Key: UKLDJPRMSDWDSL-UHFFFAOYSA-L
InChI=1/2C12H24O2.2C4H9.Sn/c2*1-2-3-4-5-6-7-8-9-10-11-12(13)14;2*1-3-4-2;/h2*2-11H2,1H3,(H,13,14);2*1,3-4H2,2H3;/q;;;;+2/p-2/rC32H64O4Sn/c1-5-9-13-15-17-19-21-23-25-27-31(33)35-37(29-11-7-3,30-12-8-4)36-32(34)28-26-24-22-20-18-16-14-10-6-2/h5-30H2,1-4H3
Key: UKLDJPRMSDWDSL-PFKFAYPQAT
SMILES: CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC
Properties of Butynorate:
Chemical formula: C32H64O4Sn
Molar mass: 631.56 g/mol
Appearance: Colourless liquid
Density: 1.066 g/mL
Melting point: 22 to 24 °C (72 to 75 °F; 295 to 297 K)
Vapor pressure: 0.2 mmHg ( 160 °C)
Quality Level: 200
Assay: 95%
Refractive index: n20/D 1.471 (lit.)
Density: 1.066 g/mL at 25 °C (lit.)
SMILES string: CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC
InChI: 1S/2C12H24O2.2C4H9.Sn/c2*1-2-3-4-5-6-7-8-9-10-11-12(13)14;2*1-3-4-2;/h2*2-11H2,1H3,(H,13,14);2*1,3-4H2,2H3;/q;;;;+2/p-2
InChI key: UKLDJPRMSDWDSL-UHFFFAOYSA-L
Molecular Weight: 631.6
Hydrogen Bond Donor Count: 0
Hydrogen Bond Acceptor Count: 4
Rotatable Bond Count: 30
Exact Mass: 632.382663
Monoisotopic Mass: 632.382663
Topological Polar Surface Area: 52.6 Ų
Heavy Atom Count: 37
Complexity: 477
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes
Related compounds of Butynorate:
Dibutyltin dioctanoate: CAS: 4731-77-5
Dibutyltin diacetate: CAS: 1067-33-0
N,N-Dimethyl-1,3-propylenediamine
N,N-Dimethyl-1,3-propylenediamine-d6
3,5-Dimethylpyrazole
Dimethyl 2-phenylbutanedioate
9-(2,6-Dimethylphenyl)-10-methylacridinium Perchlorate
Names of Butynorate:
Regulatory process names of Butynorate:
Butynorate
Butynorate
Butynorate
Butynorate
dibutyl[bis(dodecanoyloxy)] stannane
CAS names of Butynorate:
Dodecanoic acid, 1,1'-(dibutylstannylene) ester
IUPAC names of Butynorate:
[Dibutyl(dodecanoyloxy)stannyl] dodecanoate
[dibutyl(dodecanoyloxy)stannyl] dodecanoate
[dibutyl(dodecanoyloxy)stannyl]dodecanoate
dibutyl(dodecanoyloxy)stannyl] dodecanoate
Dibutylbis((1-oxododecyl)-oxy) stannane
Dibutylbis(1-oxododecyl)oxy)stannane
Dibutylbis(lauryloxy)stannan
Dibutylcín dilaurát
dibutylstannanebis(ylium) didodecanoate
dibutylstannanebis(ylium); bis(dodecanoate)
Dibutyltin didodecanoate
Butynorate
Butynorate
Butynorate
Butynorate
Butynorate
Butynorate
Butynorate, DBTL
Dibutyltin laurate
dibutyltin(2+) dilaurate
Dibutylzinndilaurat
Dodecanoic acid, 1,1'-(dibutylstannylene) ester
STANNANE, DIBUTYLBIS((1-OXODODECYL)OXY)-
Stannane, dibutylbis((1-oxododecyl)oxy)-
Stannane, dibutylbis[(1-oxododecyl)oxy]
Trade names of Butynorate:
BRB DBTDL
D-22
DBTDL
Dibutyltindilaurate (DBT)
Fomrez SUL-4E
Fomrez« catalyst SUL-4
Mark DBTL
Metatin(TM) Catalyst 712E
Metatin(TM) Catalyst 712ES
Metatin(TM) Katalysator 712E
Metatin(TM) Katalysator 712ES
SILOPREN CATALYST 162
T-CAT B12
Tinstab BL277
Other names of Butynorate:
Dibutyltindilaurate and butynorate
Synonyms of Butynorate:
Butynorate
77-58-7
Butynorate
Davainex
Tinostat
Stanclere DBTL
Dibutyltin laurate
Di-n-butyltin dilaurate
Stabilizer D-22
TVS Tin Lau
DBTL
T 12 (catalyst)
Dibutylbis(laurato)tin
Dibutyltin didodecanoate
Stavinor 1200 SN
Dibutyltin n-dodecanoate
Ongrostab BLTM
Dibutylbis(lauroyloxy)tin
Fomrez sul-4
Dibutylstannylene dilaurate
Thermolite T 12
Mark 1038
Bis(lauroyloxy)di(n-butyl)stannane
Kosmos 19
Therm chek 820
Stannane, dibutylbis[(1-oxododecyl)oxy]-
TIN DIBUTYL DILAURATE
Dibutyl-zinn-dilaurat
Neostann U 100
Tin, dibutylbis(lauroyloxy)-
Cata-Chek 820
Lankromark LT 173
TVS-TL 700
Dibutylstannium dilaurate
Stannane, bis(lauroyloxy)dibutyl-
Stannane, dibutylbis(lauroyloxy)-
Laudran di-n-butylcinicity
[dibutyl(dodecanoyloxy)stannyl] dodecanoate
Lauric acid, dibutylstannylene salt
Lauric acid, dibutyltin deriv.
dibutylstannanediyl didodecanoate
Stannane, bis(dodecanoyloxy) di-n-butyl-
T 12
KS 20
TN 12
Tin, di-n-butyl-, di(dodecanoate)
Dibutylbis(1-oxododecyl)oxy)stannane
Lauric acid, dibutylstannylene deriv.
Dodecanoic acid, 1,1'-(dibutylstannylene) ester
MFCD00008963
NCGC00166115-01
Stannane, dibutylbis((1-oxododecyl)oxy)-
DSSTox_CID_4961
DSSTox_RID_77599
DSSTox_GSID_24961
Laustan-B
CAS-77-58-7
Dibutyl-tin-dilaurate
TN 12 (catalyst)
Stavincor 1200 SN
Mark BT 11
Mark BT 18
Dibutylbis(lauroxy)stannane
Butyl norate
CCRIS 4786
DXR 81
Dibutyl-zinn-dilaurat
HSDB 5214
T 12 (VAN)
Stabilizer D 22
Laudran di-n-butylcinicity
NSC 2607
SM 2014C
EINECS 201-039-8
Dibutyltin dillaurate
Metacure T-12
Stannane, bis(dodecanoyloxy)di-n-butyl
Tin, di(dodecanoate)
di-n-Butylin dilaurate
AI3-26331
ADK STAB BT-11
Butynorate, 95%
C32H64SO4n
DTXSID6024961
NSC2607
Lauric acid, dibutyltin derivative
Dibutylbis(1-oxododecyloxy)stannane
NSC-2607
Bis(dodecanoyloxy)di-n-butylstannane
Tox21_112324
6945AF
Dibutyl[bis(dodecanoyloxy)]stannane #
Dibutylbis[(1-oxododecyl)oxy]stannane
Butynorate, SAJ first grade
Tox21_112324_1
ZINC169743348
Butynorate, Selectophore(TM)
WLN: 11VO-SN-4&4&OV11
Lauric acid, dibutylstannylene derivative
NCGC00166115-02
Di-n-butyltin dilaurate (18 - 19% Sn)
FT-0624688
E78905
EC 201-039-8
A839138
Q-200959
dodecanoic acid [dibutyl(1-oxododecoxy)stannyl] ester
201-039-8 [EINECS]
77-58-7 [RN]
Bis(lauroyloxy)di(n-butyl)stannane
DBTDL
Dibutyl[bis(dodecanoyloxy)]stannan
Dibutyl[bis(dodecanoyloxy)]stannane
Dibutyl[bis(dodecanoyloxy)]stannane
Dibutylbis(1-oxododecyloxy)stannane
Dibutylbis(lauroyloxy)tin
Butynorate
Dibutyltin dillaurate
Dibutyltin laurate
Dibutyltin n-dodecanoate
di-n-Butylin dilaurate
MFCD00008963
Stannane, dibutylbis[(1-oxododecyl)oxy]-
Tin, dibutylbis(lauroyloxy)-
Tin, di-n-butyl-, di(dodecanoate)
WH7000000
105-77-1
ADK STAB BT-11
Bis(dodecanoyloxy)di-n-butylstannane
butyl norate
butynorate
Cata-Chek 820
Dabco T-12
Davainex
DBTL
Dibutyl bis(lauroyloxy)tin
dibutyl tin dilaurate
DIBUTYL(DODECANOYLOXY)STANNYL DODECANOATE
Dibutyl[bis(dodecanoyloxy)]stannan
Dibutylbis(1-oxododecyl)oxy)stannane
Dibutylbis(laurato)tin
Dibutylbis(lauroxy)stannane
Dibutylbis(lauroyloxy)stannane
Dibutylbis(lauroyloxy)stannane, Dibutyl bis(lauroyloxy)tin
DIBUTYLBIS[(1-OXODODECYL)OXY]STANNANE
Dibutylstannium dilaurate
Dibutylstannylene dilaurate
Dibutyltin didodecanoate
Dibutyltin dilauric acid
Dibutyl-zinn-dilaurat
DI-N-BUTYLDILAURYLTIN
Di-n-butyltin didodecanoate
DI-N-BUTYLTIN DILAURATE
dodecanoic acid [dibutyl(1-oxododecoxy)stannyl] ester
Dodecanoic acid, 1,1'-(dibutylstannylene) ester
Fomrez sul-4
Kosmos 19
L4061GMT90
Lankromark LT 173
Laudran di-n-butylcinicity
Laustan-B
Metacure T-12
Neostann U 100
Stannane, bis(dodecanoyloxy) di-n-butyl-
Stannane, bis(dodecanoyloxy)di-n-butyl
Stannane, bis(lauroyloxy)dibutyl-
Stannane, dibutylbis(lauroyloxy)-
Stavinor 1200 SN
Therm chek 820
Thermolite T 12
Tin dibutyl dilaurate
Tinostat
TVS Tin Lau
TVS-TL 700
WLN: 11VO-SN-4&4&OV11