Tetramethylene glycol is a primary alcohol, and an organic compound, with the formula HOCH2CH2CH2CH2OH.
Tetramethylene glycol is a colorless viscous liquid.
Tetramethylene glycol is one of four stable isomers of butanediol.
CAS number: 112-60-7
EC number: 203-989-9
Molecular Formula: C4H10O2
Molar Mass: 90.12
Tetramethylene glycol is a straight chain glycol with hydroxyl groups on both ends.
Tetramethylene glycol is used as a raw material for high performance polyester and polyurethane resins as well as for industrial chemicals like tetrahydrofuran and gamma-butyrolactone.
Description of Tetramethylene glycol:
Tetramethylene glycol is commonly used as a solvent in the chemical industry to manufacture gamma-butyrolactone and elastic fibers like spandex.
Tetramethylene glycol is used as a cross-linking agent for thermoplastic urethanes, polyester plasticizers, paints and coatings.
Tetramethylene glycol undergoes dehydration in the presence of phosphoric acid yielded teterahydrofuran, which is an important solvent used for various applications.
Tetramethylene glycol acts an intermediate and is used to manufacture polytetramethylene ether glycol (PTMEG), polybutylene terephthalate (PBT) and polyurethane (PU).
Tetramethylene glycol finds application as an industrial cleaner and a glue remover.
Solubility of Tetramethylene glycol:
Tetramethylene glycol is miscible with water, ethanol, dimethyl sulfoxide and glycol ethers.
Tetramethylene glycol is slightly miscible with diethyl ether.
Tetramethylene glycol is immiscible with aliphatic and aromatic hydrocarbons.
Applications of Tetramethylene glycol:
Tetramethylene glycol (1,4-Butanediol (BDO), 1,4-Butylene glycol (BG), 1,4-Dihydroxy butane) is a raw material for polyester and polyurethane resins (chain extender, hard segment) that show excellent characteristics.
Tetramethylene glycol find a wide range of applications including everyday consumer products such as clothing and shoe soles, consumer durables such as electrical appliances and cars, industrial materials such as machine parts, as well as medical products.
Tetramethylene glycol is anticipated that the use of these polymers will continue to expand.
Main Applications of Tetramethylene glycol:
-PBT (Polybutylene terephthalate) Resin Raw Material
Because Tetramethylene glycol is used as a raw materail, PBT is a great engineering plastic with low water-absorbance and an excellent balance of mechanical and electrical properties.
Applications are expanding beyond the original electrical/electronic parts and automotive parts markets.
-Polyurethane Resin Raw Material
By using Tetramethylene glycol for the chain extender, urethane elastomers can be made with excellent mechanical properties and high resistances to heat, oil, and impact.
-Other Polyester Raw Materials
Tetramethylene glycol is widely used to make various polyester resins and plasticizers.
-Raw Material for Industrial Chemicals (Tetrahydrofuran, Gamma-Butyrolactone)
Tetrahydrofuran and gamma-butyrolactone are produced indutrially by dehydration or dehydrogenation of 14BG.
Uses of Tetramethylene glycol:
Tetramethylene glycol is used as a chromatographic analysis reagent and also used in organic synthesis 1,4-butanediol has a wide range of uses.
More than half of Tetramethylene glycol is used in the production of tetrahydrofuran in the United States and Western Europe, followed by the production of γ-butyrolactone and polybutylene terephthalate, which are rapidly developing engineering plastics; Tetramethylene glycol as a chain extender and polyester raw material, Tetramethylene glycol is used to produce polyurethane elastomers and flexible polyurethane foams; esters made of Tetramethylene glycol are good plasticizers for cellulose, polyvinyl chloride, polyacrylate and polyester.
Tetramethylene glycol has good hygroscopicity and flexibility, and can be used as a gelatin softener and water absorbent, cellophane and other unused paper treatment agents.
Tetramethylene glycol can also prepare N-methylpyrrolidone, N-vinylpyrrolidone and other pyrrolidone derivatives, and is also used to prepare vitamin B6, pesticides, herbicides, and solvents that act on various processes, Plasticizers, lubricants, humidification agents, softness, adhesives and brighteners in the electroplating industry.
Reagents for chemical analysis, used as gas chromatography stationary liquid.
Tetramethylene glycol is used as solvent, non-toxic antifreeze, food emulsifier, moisture absorbent, used in organic synthesis.
Pharmaceutical, food industry.
Solvent.
Humectant.
Intermediate of plasticizer.
Crosslinkers for the manufacture of polyurethane elasto bodies.
Organic synthesis.
Manufacture of tetrahydrofuran.
Tetramethylene glycol is a polymer consisting of ethylene glycol monomer units and two terminal hydroxyl groups.
The hydroxyl groups can react to further derivatize the compound.
Ethylene glycol compounds have hydrophilic characteristics.
The solubility of the polymer increases as the number of ethylene glycol groups increase.
Description of Tetramethylene glycol:
Catalogue Number: 808619
Synonyms: Tetraglycol
Description: Tetraethylene glycol
About Tetramethylene glycol:
Tetramethylene glycol is registered under the REACH Regulation and is manufactured in and / or imported to the European Economic Area, at ≥ 10 to < 100 tonnes per annum.
Tetramethylene glycol is used in formulation or re-packing, at industrial sites and in manufacturing.
Consumer Uses of Tetramethylene glycol:
ECHA has no public registered data indicating whether or in which chemical products Tetramethylene glycol might be used.
ECHA has no public registered data on the routes by which Tetramethylene glycol is most likely to be released to the environment.
Article service life of Tetramethylene glycol:
ECHA has no public registered data on the routes by which Tetramethylene glycol is most likely to be released to the environment.
ECHA has no public registered data indicating whether or into which articles Tetramethylene glycol might have been processed.
Widespread uses by professional workers of Tetramethylene glycol:
ECHA has no public registered data indicating whether or in which chemical products Tetramethylene glycol might be used.
ECHA has no public registered data on the types of manufacture using Tetramethylene glycol.
ECHA has no public registered data on the routes by which Tetramethylene glycol is most likely to be released to the environment.
Formulation or re-packing of Tetramethylene glycol:
ECHA has no public registered data indicating whether or in which chemical products Tetramethylene glycol might be used.
Release to the environment of Tetramethylene glycol can occur from industrial use: formulation of mixtures.
Uses at industrial sites of Tetramethylene glycol:
Tetramethylene glycol is used in the following products: adhesives and sealants, coating products, inks and toners and polymers.
Tetramethylene glycol is used for the manufacture of: chemicals.
Release to the environment of Tetramethylene glycol can occur from industrial use: in the production of articles and for thermoplastic manufacture.
Manufacture of Tetramethylene glycol:
Release to the environment of Tetramethylene glycol can occur from industrial use: manufacturing of .
Product Information about Tetramethylene glycol:
CAS number: 112-60-7
EC number: 203-989-9
Hill Formula: C₈H₁₈O₅
Chemical formula: HO(CH₂CH₂O)₄H
Molar Mass: 194.23 g/mol
HS Code: 2909 49 80
Tetramethylene glycol is a biodegradable primary alcohol with a high melting point.
We're proud to offer you the ability to buy BDO online in the United States.
TYPICAL APPLICATIONS of Tetramethylene glycol:
Tetramethylene glycol is also used as an intermediate to make polyurethane that is used in auto bumpers and dashboards.
Tetramethylene glycol is also used in polyester coatings.
Tetramethylene glycol reacts with terephthalic acid to produce polybutylene terephthalate (PBT), as well as reacting with adipic acid to yield polyesters with biodegradable attributes.
Tetramethylene glycol will produce polymers which exhibit greater hydrophobicity, as well as superior hydrolysis resistance and improved low temperature malleability over polymers produced from ethylene glycol.
Physicochemical Information of Tetramethylene glycol:
Boiling point: 327 - 328 °C (1013 hPa)
Density: 1.120 g/cm3 (25 °C)
Explosion limit: 0.5 - 3.4 %(V)
Flash point: 204 °C
Ignition temperature: 340 °C DIN 51794
Melting Point: -9.4 °C
pH value: 8.5 - 9.0 (500 g/l, H₂O, 20 °C)
Vapor pressure: <0.1 hPa (26 °C)
Viscosity kinematic: 50.13 mm2/s (20.65 °C)
Solubility: 1000 g/l
Tetramethylene glycol is the organic compound with the formula HOCH2CH2CH2CH2OH.
Tetramethylene glycol is derived from butane by placement of alcohol groups at each end of the chain.
Tetramethylene glycol is one of four stable isomers of butanediol.
Description of Tetramethylene glycol:
Tetramethylene glycol is used in synthesis of polyurethane and polyesters , paints and coatings, copolyester hot melt and solvent-borne adhesives.
Introduction to Tetramethylene glycol:
Tetramethylene glycol is an industrial chemical, and is illicitly used as a substitute to gamma-hydroxybutyric acid (GHB).
Tetramethylene glycol is structurally similar to GHB and there is a large body of evidence to confirm that GBL and BD are converted to GHB after oral administration.
Licit Uses:
Tetramethylene glycol is a commonly used industrial chemical intermediate.
Worldwide yearly production of Tetramethylene glycol is measured in the millions of metric tons.
Chemistry:
Tetramethylene glycol has the molecular formula C4H10O2 and the molecular weight 90.12 g/mol.
Tetramethylene glycol is a colorless, viscous liquid.
Tetramethylene glycol is a chemical.
Tetramethylene glycol's used as a source of gamma-hydroxybutyrate (GHB), a recreational drug with euphoric and sedative effects.
Tetramethylene glycol is converted to GHB in the body.
Tetramethylene glycol slows down the brain, which can cause loss of consciousness along with dangerous slowing of breathing and other vital functions.
People use Tetramethylene glycol for muscle strength, obesity, insomnia, and other purposes, but there is no good scientific evidence to support any use.
Tetramethylene glycol is also unsafe.
Tetramethylene glycol is a colorless, viscous liquid derived from butane by placement of alcohol groups at each end of its molecular chain and is one of four stable isomers of butanediol.
The hydroxyl function of each end group of the Butanediol reacts with different mono- and bifunctional reagents: for example with dicarboxylic acids to polyesters, with diisocyanates to polyurethanes, or with phosgene to polycarbonates.
Tetramethylene glycol is a high-quality intermediate.
Tetramethylene glycol and its derivatives are widely used for producing plastics, solvents, electronic chemicals and elastic fibers.
Additionally Tetramethylene glycol is also a building block for the synthesis of polyesterpolyols and polyetherpolyols.
BASF is the most significant producer of Tetramethylene glycol and its derivatives worldwide.
Storage and Handling of Tetramethylene glycol:
Tetramethylene glycol is hygroscopic and will be degraded by oxygen, so the storage container should be sealed with dry nitrogen.
Tetramethylene glycol is recommended that storage be at 25-40℃.
Below 20℃ Tetramethylene glycol will be solid, but can be mellted by careful heating.
To melt solidified Tetramethylene glycol in drums, hold overnight at 50-70℃.
Tetramethylene glycol is classified under the Japanese Fire Services Act as a hazardous material, Class 4, Petroleums No.3, water soluble, Hazardous Rank III.
Volatility is low, and Tetramethylene glycol is unlikely to catch fire by itself at room temperature.
However, in case it is burning, dry chemical, foam (alcohol resistant), or large amounts of water are effective.
Tetramethylene glycol has relatively low toxicity and is a relatively safe chemical.
When handling, however, protective equipment such as protective gloves and goggles should be worn.
Physico-chemical Properties of Tetramethylene glycol:
Molecular Formula: C4H10O2
Molar Mass: 90.12
Density: 1.017 g/mL at 25 °C (lit.)
Melting Point: 16 °C (lit.)
Boling Point: 230 °C (lit.)
Flash Point: 135 °C
Water Solubility: Miscible
Solubility: Slightly soluble in ether, miscible with water, soluble in ethanol, etc.
Vapor Density: 3.1 (vs air)
Formula: C12H26O5
Molecular mass: 250.3
Boiling point: 304°C
Melting point: -33°C
Density: 1.0 g/cm³
Solubility in water: miscible
Vapour pressure, Pa at 20°C: <0.01
Relative vapour density (air = 1): 8.6
Relative density of the vapour/air-mixture at 20°C (air = 1): 1.00
Flash point: 166°C o.c.
Octanol/water partition coefficient as log Pow: -0.26
Viscosity: 13.9 mm²/s at 20°C
Nature:
-Colorless oily liquid, flammable, miscible with water.
-Soluble in methanol, ethanol, acetone, slightly soluble in ether.
-Boiling point 228 °c.
-Melting point 20.2 °c.
-Flash point (Open Cup) 121 °c.
-The relative density was 1. 0171.
-Refractive index 4461.
Tetramethylene glycol is flammable.
Tetramethylene glycol tastes bitter.
Tetramethylene glycol can be miscible with water.
Tetramethylene glycol is soluble in alcohol, slightly soluble in ether.
Tetramethylene glycol is solely solidified in the coolant to form colorless needle-like crystals, react with dilute nitric acid to form succinic acid, and produce precipitation when encountering potassium carbonate solution
Uses of Tetramethylene glycol:
Tetramethylene glycol is mainly used in the manufacture of tetrahydrofuran, γ-butyrolactone, polyurethane and thermoplastic engineering plastic PBT resin.
Tetramethylene glycol can also be prepared N-methyl pyrrolidone, N-vinyl pyrrolidone and other pyrrolidone derivatives, also used in the preparation of vitamin B6, pesticides, herbicides and used as a variety of process solvents, plasticizers, lubricants, moisturizers, softeners, adhesives and brighteners for the electroplating industry.
Appearance: Transparent micro viscous liquid
Color: Clear colorless
Odor: Odorless
BRN: 1633445
pKa: 14.73±0.10(Predicted)
PH: 7-8 (500g/l, H2O, 20℃)
Storage Condition: Store Tetramethylene glycol below +30°C.
Stability: Stable. Combustible. Incompatible with strong oxidizing agents, mineral acids, acid chlorides, acid anhydrides.
Sensitive: Hygroscopic
Explosive Limit: 1.95-18.3%(V)
Refractive Index: n20/D 1.445(lit.)
MDL: MFCD00002968
Physical and Chemical Properties of Tetramethylene glycol:
Tetramethylene glycol is a colorless oily liquid.
melting point: 20.2 ℃
boiling point: 228 ℃
relative density: 1.0171
refractive index: 1.4461
flash point: 121 ℃
Solubility of Tetramethylene glycol:
Tetramethylene glycol solubility is miscible with water.
Tetramethylene glycol is soluble in methanol, ethanol, acetone, slightly soluble in ether.
Uses of Tetramethylene glycol:
Tetramethylene glycol is used as solvents and moisturizers, but also for the preparation of plasticizers, drugs, polyester resins, polyurethane resins, etc
Synthesis of Tetramethylene glycol:
In industrial chemical synthesis, acetylene reacts with two equivalents of formaldehyde to form butyne-1,4-diol.
Hydrogenation of butyne-1,4-diol gives Tetramethylene glycol.
Tetramethylene glycol is also made on an industrial scale from maleic anhydride in the Davy process, which is first converted to the methyl maleate ester, then hydrogenated.
Other routes are from butadiene, allyl acetate and succinic acid.
A biological route to BD has been commercialized that uses a genetically modified organism.
The biosynthesis proceeds via 4-hydroxybutyrate.
Industrial uses of Tetramethylene glycol:
Tetramethylene glycol is used industrially as a solvent and in the manufacture of some types of plastics, elastic fibers and polyurethanes.
In organic chemistry, Tetramethylene glycol is used for the synthesis of γ-butyrolactone (GBL).
In the presence of phosphoric acid and high temperature, Tetramethylene glycol dehydrates to the important solvent tetrahydrofuran.
At about 200 °C in the presence of soluble ruthenium catalysts, the diol undergoes dehydrogenation to form butyrolactone.
Tetramethylene glycol is used to synthesize 1,4-Butanediol diglycidyl ether which is then used as a reactive diluent for epoxy resins.
Use as a recreational drug:
FDA warning against products containing GHB and its prodrugs, such as Tetramethylene glycol.
Tetramethylene glycol is also used as a recreational drug known by some users as "One Comma Four", "Liquid Fantasy", "One Four Bee" or "One Four B-D-O".
A few Federal Courts have stated that Tetramethylene glycol exerts effects similar to gamma-hydroxybutyrate (GHB), which is a metabolic product of 1,4-butanediol.
But other Federal courts have ruled that it is not.
Pharmacokinetics:
Tetramethylene glycol is rapidly converted into gamma-hydroxybutyric acid by the enzymes alcohol dehydrogenase and aldehyde dehydrogenase, and differing levels of these enzymes may account for differences in effects and side effects between users.
While co-administration of ethanol and GHB already poses serious risks, co-administration of ethanol with Tetramethylene glycol will interact considerably and has many other potential risks.
This is because the same enzymes that are responsible for metabolizing alcohol also metabolize Tetramethylene glycol so there is a strong chance of a dangerous drug interaction.
Emergency room patients who overdose on both ethanol and Tetramethylene glycol often present with symptoms of alcohol intoxication initially and as the ethanol is metabolized the Tetramethylene glycol is then able to better compete for the enzyme and a second period of intoxication ensues as the Tetramethylene glycol is converted into GHB.
Names:
Preferred IUPAC name
Butane-1,4-diol
Other names:
Tetramethylene glycol
Pharmacodynamics:
Tetramethylene glycol seems to have two types of pharmacological actions.
The major psychoactive effects of Tetramethylene glycol are because it is metabolized into GHB; however there is a study suggesting that 1,4-butanediol may have potential alcohol-like pharmacological effects on its own.
The study arrived at this conclusion based on the finding that Tetramethylene glycol coadministered with ethanol led to potentiation of some of the behavioral effects of ethanol.
However, potentiation of ethanol's effects may simply be caused by competition for the alcohol dehydrogenase and aldehyde dehydrogenase enzymes with co-administered 1,4-butanediol.
The shared metabolic rate-limiting steps thus leads to slowed metabolism and clearance for both compounds including ethanol's known toxic metabolite acetaldehyde.
Another study found no effect following intracerebroventricular injection of Tetramethylene glycol in rats.
This contradicts the hypothesis of Tetramethylene glycol having inherent alcohol-like pharmacological effects.
Like gamma-hydroxybutyric acid, Tetramethylene glycol is safe only in small amounts.
Adverse effects in higher doses include nausea, vomiting, dizziness, sedation, vertigo, and potentially death if ingested in large amounts.
Anxiolytic effects are diminished and side effects increased when used in combination with alcohol.
Identifiers of Tetramethylene glycol:
CAS Number: 110-63-4
CHEBI: 41189
ChEMBL: ChEMBL171623
ChemSpider: 13835209
DrugBank: DB01955
ECHA InfoCard: 100.003.443
EC Number: 203-786-5
PubChem CID: 8064
RTECS number: EK0525000
UNII: 7XOO2LE6G3
CompTox Dashboard (EPA): DTXSID2024666
Legality:
While Tetramethylene glycol is not currently scheduled federally in the United States, a number of states have classified 1,4-butanediol as a controlled substance.
Individuals have been prosecuted for possession of Tetramethylene glycol under the Federal Analog Act as substantially similar to GHB.
A federal case in New York in 2002 ruled that Tetramethylene glycol could not be considered an analog of GHB under federal law, but that decision was later overturned by the Second Circuit.
A jury in Federal District Court in Chicago found that Tetramethylene glycol was not an analog of GHB under federal law, which was not disputed on the case's appeal to the Seventh Circuit Court of Appeals, however this finding did not affect the outcome of the case.
In the United Kingdom, Tetramethylene glycol was scheduled in December 2009 (along with another GHB precursor, gamma-butyrolactone) as a Class C controlled substance.
In Germany, Tetramethylene glycol is not explicitly illegal, but might also be treated as illegal if used as a drug.
Tetramethylene glycol is controlled as a Schedule VI precursor in Canada.
A toy called "Bindeez" ("Aqua Dots" in North America) was recalled by the distributor in November 2007 because of the presence of Tetramethylene glycol.
The toy consists of small beads that stick to each other by sprinkling water.
Tetramethylene glycol was detected by GC-MS.
The production plant seems to have intended to cut costs by replacing less toxic pentane-1,5-diol with Tetramethylene glycol.
2021 poisoning at Darmstadt Technical University
In August 2021, several people fell severely ill after consuming drinks at building L2.01 at the Lichtwiese Campus of Darmstadt Technical University, Germany.
Seven showed severe symptoms, two were transported to a hospital in Frankfurt am Main, and a 30-year-old person was, for a time, in a critical state.
Tetramethylene glycol had been detected in milk packages, as well as in water filters.
At the location, detectives also found bromophenols and dicyclohexylamine.
Properties of Tetramethylene glycol:
Chemical formula: C4H10O2
Molar mass: 90.122 g·mol−1
Density: 1.0171 g/cm3 (20 °C)
Melting point: 20.1 °C (68.2 °F; 293.2 K)
Boiling point: 235 °C (455 °F; 508 K)
Solubility in water: Miscible
Solubility in ethanol: Soluble
Magnetic susceptibility (χ): -61.5·10−6 cm3/mol
Refractive index (nD): 1.4460 (20 °C)
Synonym(s):
Bis[2-(2-hydroxyethoxy)ethyl] ether
Tetra(ethylene glycol)
Tetraglycol
Linear Formula:
HO(CH2CH2O)3CH2CH2OH
CAS Number:
112-60-7
Molecular Weight:
194.23
Beilstein:
1634320
EC Number:
203-989-9
MDL number:
MFCD00002879
eCl@ss:
39020714
PubChem Substance ID:
24846965
NACRES:
NA.23
DESCRIPTION of Tetramethylene glycol:
General description of Tetramethylene glycol:
An oligomer of polyethylene glycol, tetra (ethylene glycol) (TEG) is a transparent, colorless, odorless, low volatility, hygroscopic liquid soluble in ethyl alcohol and very soluble in water.
Applications of Tetramethylene glycol:
Tetramethylene glycol is used for the synthesis of tetraethylene glycol metha acrylate monomer.
Glow discharge plasma deposition of TEG renders surfaces resistant to protein adsorption and cellular attachment.
PROPERTIES of Tetramethylene glycol:
vapor density:
6.7 (vs air)
Quality Level:
200
vapor pressure:
<0.01 mmHg
assay:
99%
mol wt:
average Mn 200
refractive index:
n20/D 1.459 (lit.)
bp:
314 °C (lit.)
mp:
−5.6 °C (lit.)
density:
1.125 g/mL at 25 °C (lit.)
Ω-end:
hydroxyl
α-end:
hydroxyl
SMILES string:
OCCOCCOCCOCCO
InChI:
1S/C8H18O5/c9-1-3-11-5-7-13-8-6-12-4-2-10/h9-10H,1-8H2
InChI key:
UWHCKJMYHZGTIT-UHFFFAOYSA-N
Synonym(s):
1,4-Butylene glycol
Tetramethylene glycol
Linear Formula:
HO(CH2)4OH
CAS No.:
110-63-4
Molecular Weight:
90.12
EC No.:
203-786-5
Beilstein No.:
1633445
Regulatory process names:
1,4-butanediyl diacrylate
1,4-butanediyl diacrylate
1,4-butyleneglycol diacrylate
2-Propenoic acid, 1,1'-(1,4-butanediyl) ester
tetramethylene diacrylate
tetramethylene diacrylate; 1,4-butyleneglycol diacrylate
Translated names:
(bután-1,4-diyl)-diakrylát (sk)
1,4- butilēnglikola diakrilāts (lv)
1,4-butandiol diacrilato (it)
1,4-butandiol diakrilat (sl)
1,4-butandioldiacrylat (da)
1,4-Butandioldiacrylat (de)
1,4-butandioldiakrilatas (lt)
1,4-butandioldiakrylat (no)
1,4-butandioldiakrylat (sv)
1,4-butileneglicol diacrilat (ro)
1,4-butilenglikol diakrilat (hr)
1,4-butilén-glikol-diakrilát (hu)
1,4-butylenglycoldiacrylat (da)
1,4-butylenglykol-diakrylát (cs)
1,4-Butylenglykoldiacrylat (de)
1,4-butylenglykoldiakrylat (no)
1,4-butüleenglükooldiakrülaat (et)
1,4-бутиленгликол диакрилат (bg)
butan-1,4-diyl-diakrylát (cs)
diacrilato de 1,4-butilenglicol (es)
diacrilato de 1,4-butilenoglicol (pt)
diacrilato de 1,4-tetrametileno (es)
diacrilato de tetrametileno (pt)
diacrylaat van 1,4-butaandiol (nl)
diacrylaat van 1,4-butyleenglycol (nl)
diacrylate de 1,4-butylèneglycol (fr)
diacrylate de tétraméthylène; diacrylate de 1,4-butylène glycol (fr)
diakrylan butano-1,4-diylu (pl)
diakrylan glikolu 1,4-butylenowego (pl)
diakrylan tetrametylenu (pl)
diakrylát 1,4-butylénglykolu (sk)
tetrametilen diacrilat (ro)
tetrametilen diakrilat (hr)
tetrametilen diakrilat (sl)
tetrametileno diakrilatas (lt)
tetrametilén-diakrilát (hu)
tetrametilēndiakrilāts (lv)
Tetrametyleenidiakrylaatti (fi)
Tetrametüleendiakrülaat (et)
διακρυλικός 1,4-βουτανοδιεστέρας (el)
тетраметилен диакрилат (bg)
CAS names:
2-Propenoic acid, 1,1'-(1,4-butanediyl) ester
IUPAC names:
1,4 butanedioldiacrylate
1,4-Bis(acryloyloxy)butane (stabilized with MEHQ)
1,4-Butandioldiacrylat
1,4-Butanediyl diacrylate
1,4-butanediyl diacrylate
1,4-butyleneglycol diacrylate
1-4-butyleneglycol diacrylate
4-(prop-2-enoyloxy)butyl prop-2-enoate
4-prop-2-enoyloxybutyl prop-2-enoate
BDDA
butane-1,4-diyl bisacrylate
TETRAMETHYLENE DIACRYLATE
Trade names:
1,4-Butanediol diacrylate
1,4-Butanediol, diacrylate (8CI)
1,4-Butylene diacrylate
1,4-Butylene glycol diacrylate
2-Propenoic acid, 1,4-butanediyl ester (9CI)
Acrylic acid, tetramethylene ester (6CI, 7CI, 8CI)
Laromer BDDA
SR 213
Tetramethylene diacrylate
Tetramethylene glycol diacrylate
Other identifiers:
1070-70-8
119518-37-5
119518-37-5
138790-64-4
138790-64-4
1934258-70-4
1934258-70-4
607-119-00-2
Synonyms:
BDO
1,4-Butanediol
1,4-BUTANEDIOL
butane-1,4-diol
butane-1,1-diol
BUTANEDIOL, 1,4-
AKOS BBS-00004303
1,4-DIHYDROXYBUTANE
1,4-BUTYLENE GLYCOL
1,4-Butylene glycol
TETRAMETHYLENE GLYCOL
Tetramethylene glycol
VERSALINK CURATIVE 1,4 BDO
1,4-BUTANEDIOL
Butane-1,4-diol
110-63-4
1,4-Butylene glycol
Tetramethylene glycol
1,4-Dihydroxybutane
1,4-Tetramethylene glycol
Tetramethylene 1,4-diol
Sucol B
1,4-BD
DIOL 14B
HO(CH2)4OH
NSC 406696
HOCH2CH2CH2CH2OH
7XOO2LE6G3
CHEBI:41189
NSC-406696
Agrisynth B1D
BDO
BU1
CAS-110-63-4
CCRIS 5984
HSDB 1112
EINECS 203-786-5
MFCD00002968
UNII-7XOO2LE6G3
BRN 1633445
AI3-07553
4-hydroxybutanol
1,4butanediol
1.4-butanediol
Dabco BDO
1,4-butandiol
1,4-butane diol
1,4-butane-diol
butane 1,4-diol
butane diol-1,4
butane-1-4-diol
1,4- butandiol
Butan-1.4-diol
1.4 - butanediol
1,4 butylene glycol
1,4-Butanediol, 99%
EC 203-786-5
WLN: Q4Q
4-01-00-02515 (Beilstein Handbook Reference)
MLS001061198
CHEMBL171623
1,4-BUTANEDIOL [MI]
DTXSID2024666
1,4-BUTANEDIOL [HSDB]
1,4-BUTANEDIOL [INCI]
HMS3039N12
ZINC1599375
Tox21_202245
Tox21_303040
NSC406696
STL283940
AKOS000118735
1,4-Butanediol, for synthesis, 98%
CS-W016669
DB01955
1,4-Butanediol, ReagentPlus(R), 99%
NCGC00090733-01
NCGC00090733-02
NCGC00257119-01
NCGC00259794-01
BP-21418
SMR000677930
1,4-Butanediol, ReagentPlus(R), >=99%
B0680
FT-0606811
F71206
1,4-Butanediol, Vetec(TM) reagent grade, 98%
Q161521
J-503971
J-512798
F0001-0222