Cyclopentolate (CED0004561)

Record Information
Version1.0
Creation Date2016-05-25 18:24:06 UTC
Update Date2026-08-19 21:39:16 UTC
SynCED IDCED0004561
Secondary Accession Numbers
  • CHEM022213
Identification
Common NameCyclopentolate
ClassSmall Molecule
Description
Cyclopentolate is an organic compound with the formula C17H25NO3 and an average molecular weight of 291.39 g/mol. Cyclopentolate belongs to the benzene and substituted derivatives, a class of benzenoids within the organic compounds. This compound is recorded as being found in or released from seven distinct sources. These include healthcare, pharmaceuticals, and veterinary products, specifically as mydriatics and cycloplegics. It is also associated with household cleaning and consumer products, such as tobacco smoke filters, cigar cigarettes, and other smoking requisites. Additionally, it is linked to electrical and electronic equipment, including electrodes, electrically stimulated smoking devices, and conductors or conductive bodies characterized by the conductive materials. The recorded route of exposure for this substance is ophthalmic. In terms of biological activity, cyclopentolate acts on two recorded protein targets. It functions as an antagonist of the muscarinic acetylcholine receptor M1 (CHRM1) and the muscarinic acetylcholine receptor M5 (CHRM5).
Contaminant Type
  • Human Neurotoxin
Chemical Structure
Synonyms
ValueSource
(+-)-CyclopentolateChEBI
1-Hydroxy-alpha-phenylcyclopentaneacetic acid 2-(dimethylamino)ethyl esterChEBI
2-(Dimethylamino)ethyl 1-hydroxy-alpha-phenylcyclopentaneacetateChEBI
2-(Dimethylamino)ethyl 2-(1-hydroxycyclopentyl)-2-phenylacetateChEBI
2-Phenyl-2-(1-hydroxycyclopentyl)ethanoic acid beta-(dimethylamino)ethyl esterChEBI
alpha-(1-Hydroxycyclopentyl)benzeneacetic acid 2-(dimethylamino)ethyl esterChEBI
beta-(Dimethylamino)ethyl (1-hydroxycyclopentyl)phenylacetateChEBI
beta-Dimethylaminoethyl (1-hydroxycyclopentyl)phenylacetateChEBI
CiclopentolatoChEBI
CyclopentolatumChEBI
Bell pentolateKegg
(+-)-Cyclopentolic acidGenerator
1-Hydroxy-a-phenylcyclopentaneacetate 2-(dimethylamino)ethyl esterGenerator
1-Hydroxy-a-phenylcyclopentaneacetic acid 2-(dimethylamino)ethyl esterGenerator
1-Hydroxy-alpha-phenylcyclopentaneacetate 2-(dimethylamino)ethyl esterGenerator
1-Hydroxy-α-phenylcyclopentaneacetate 2-(dimethylamino)ethyl esterGenerator
1-Hydroxy-α-phenylcyclopentaneacetic acid 2-(dimethylamino)ethyl esterGenerator
2-(Dimethylamino)ethyl 1-hydroxy-a-phenylcyclopentaneacetateGenerator
2-(Dimethylamino)ethyl 1-hydroxy-a-phenylcyclopentaneacetic acidGenerator
2-(Dimethylamino)ethyl 1-hydroxy-alpha-phenylcyclopentaneacetic acidGenerator
2-(Dimethylamino)ethyl 1-hydroxy-α-phenylcyclopentaneacetateGenerator
2-(Dimethylamino)ethyl 1-hydroxy-α-phenylcyclopentaneacetic acidGenerator
2-(Dimethylamino)ethyl 2-(1-hydroxycyclopentyl)-2-phenylacetic acidGenerator
2-Phenyl-2-(1-hydroxycyclopentyl)ethanoate b-(dimethylamino)ethyl esterGenerator
2-Phenyl-2-(1-hydroxycyclopentyl)ethanoate beta-(dimethylamino)ethyl esterGenerator
2-Phenyl-2-(1-hydroxycyclopentyl)ethanoate β-(dimethylamino)ethyl esterGenerator
2-Phenyl-2-(1-hydroxycyclopentyl)ethanoic acid b-(dimethylamino)ethyl esterGenerator
2-Phenyl-2-(1-hydroxycyclopentyl)ethanoic acid β-(dimethylamino)ethyl esterGenerator
a-(1-Hydroxycyclopentyl)benzeneacetate 2-(dimethylamino)ethyl esterGenerator
a-(1-Hydroxycyclopentyl)benzeneacetic acid 2-(dimethylamino)ethyl esterGenerator
alpha-(1-Hydroxycyclopentyl)benzeneacetate 2-(dimethylamino)ethyl esterGenerator
Α-(1-hydroxycyclopentyl)benzeneacetate 2-(dimethylamino)ethyl esterGenerator
Α-(1-hydroxycyclopentyl)benzeneacetic acid 2-(dimethylamino)ethyl esterGenerator
b-(Dimethylamino)ethyl (1-hydroxycyclopentyl)phenylacetateGenerator
b-(Dimethylamino)ethyl (1-hydroxycyclopentyl)phenylacetic acidGenerator
beta-(Dimethylamino)ethyl (1-hydroxycyclopentyl)phenylacetic acidGenerator
Β-(dimethylamino)ethyl (1-hydroxycyclopentyl)phenylacetateGenerator
Β-(dimethylamino)ethyl (1-hydroxycyclopentyl)phenylacetic acidGenerator
b-Dimethylaminoethyl (1-hydroxycyclopentyl)phenylacetateGenerator
b-Dimethylaminoethyl (1-hydroxycyclopentyl)phenylacetic acidGenerator
beta-Dimethylaminoethyl (1-hydroxycyclopentyl)phenylacetic acidGenerator
Β-dimethylaminoethyl (1-hydroxycyclopentyl)phenylacetateGenerator
Β-dimethylaminoethyl (1-hydroxycyclopentyl)phenylacetic acidGenerator
Bell pentolic acidGenerator
Cyclopentolic acidGenerator
CyclopentoiateHMDB
CyclopentylateHMDB
DiopentolateHMDB
CyclogylHMDB
Chemical FormulaC17H25NO3
Average Molecular Mass291.385 g/mol
Monoisotopic Mass291.183 g/mol
CAS Registry Number512-15-2
IUPAC Name2-(dimethylamino)ethyl 2-(1-hydroxycyclopentyl)-2-phenylacetate
Traditional Namecyclopentolate
SMILESCN(C)CCOC(=O)C(C1=CC=CC=C1)C1(O)CCCC1
InChI IdentifierInChI=1S/C17H25NO3/c1-18(2)12-13-21-16(19)15(14-8-4-3-5-9-14)17(20)10-6-7-11-17/h3-5,8-9,15,20H,6-7,10-13H2,1-2H3
InChI KeySKYSRIRYMSLOIN-UHFFFAOYSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as benzene and substituted derivatives. These are aromatic compounds containing one monocyclic ring system consisting of benzene.
KingdomOrganic compounds
Super ClassBenzenoids
ClassBenzene and substituted derivatives
Sub ClassNot Available
Direct ParentBenzene and substituted derivatives
Alternative Parents
Substituents
  • Monocyclic benzene moiety
  • Cyclopentanol
  • Cyclic alcohol
  • Tertiary alcohol
  • Amino acid or derivatives
  • Carboxylic acid ester
  • Tertiary aliphatic amine
  • Tertiary amine
  • Carboxylic acid derivative
  • Monocarboxylic acid or derivatives
  • Amine
  • Hydrocarbon derivative
  • Organic oxide
  • Organopnictogen compound
  • Alcohol
  • Carbonyl group
  • Organic oxygen compound
  • Organic nitrogen compound
  • Organonitrogen compound
  • Organooxygen compound
  • Aromatic homomonocyclic compound
Molecular FrameworkAromatic homomonocyclic compounds
External Descriptors
Biological Properties
StatusDetected and Not Quantified
OriginNot Available
Cellular LocationsNot Available
Biofluid LocationsNot Available
Tissue LocationsNot Available
ApplicationsNot Available
Biological Roles
Chemical RolesNot Available
Organoleptic EffectsNot Available
Physical Properties
StateNot Available
AppearanceNot Available
Experimental Properties
PropertyValue
Melting PointNot Available
Boiling PointNot Available
SolubilityNot Available
Predicted Properties
PropertyValueSource
Water Solubility1.5 g/LALOGPS
logP2.09ALOGPS
logP2.32ChemAxon
logS-2.3ALOGPS
pKa (Strongest Acidic)14.19ChemAxon
pKa (Strongest Basic)8.42ChemAxon
Physiological Charge1ChemAxon
Hydrogen Acceptor Count3ChemAxon
Hydrogen Donor Count1ChemAxon
Polar Surface Area49.77 ŲChemAxon
Rotatable Bond Count7ChemAxon
Refractivity82.81 m³·mol⁻¹ChemAxon
Polarizability32.51 ųChemAxon
Number of Rings2ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterYesChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Spectra
Spectra
Spectrum TypeDescriptionSplash KeyDeposition DateView
GC-MSGC-MS Spectrumsplash10-0a4i-9000000000-0f0d4362f3985858a9e0Not AvailableView Spectrum
GC-MSGC-MS Spectrumsplash10-0a4i-9000000000-0f0d4362f3985858a9e0Not AvailableView Spectrum
Predicted GC-MSPredicted GC-MS Spectrumsplash10-0a4i-9310000000-1b840cdae4d0a8b51c1cNot AvailableView Spectrum
Predicted GC-MSPredicted GC-MS Spectrumsplash10-0a4j-9160000000-9def24a4ea67412da486Not AvailableView Spectrum
Predicted GC-MSPredicted GC-MS SpectrumNot AvailableNot AvailableView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrumsplash10-00dl-5290000000-7db0b218f03ba755d12cNot AvailableView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrumsplash10-00di-9240000000-de729816cbf8bd6c1f4cNot AvailableView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrumsplash10-00rl-9200000000-f9603efdb4791c613d6aNot AvailableView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrumsplash10-0006-2190000000-a63273dff0bd060cba13Not AvailableView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrumsplash10-0aor-7980000000-2381615fef81f1f71dd9Not AvailableView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrumsplash10-004r-9200000000-4ae6271cc9d0bc0f9449Not AvailableView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrumsplash10-0006-0090000000-586236b5df6bd5b89376Not AvailableView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrumsplash10-00di-9870000000-c8300495640521c4c24aNot AvailableView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrumsplash10-05fu-9510000000-282f90927a86ab03806eNot AvailableView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrumsplash10-002f-2690000000-8f965caa4a5020612863Not AvailableView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrumsplash10-00bc-4920000000-2d0e7b93bf17b10c75c8Not AvailableView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrumsplash10-0005-9310000000-e6335b8c4b16ebf862afNot AvailableView Spectrum
Toxicity Profile
Toxicity Values
Toxicity ValueOrganismDose DescriptorRoute of ExposurePredicted or ExperimentalToxicity RatingReference
692.0 Log mg/kg [390:1200]RatLD50oralpredictedNot AvailableNot Available
Toxicity / Toxin ClassNot Available
Mechanism of ToxicityNot Available
Carcinogenicity (IARC Classification)Not Available
Minimum Risk LevelNot Available
SymptomsNot Available
TreatmentNot Available
Health Effects
Health EffectRelationshipDirectionDescriptionReference
corneal edemaNot AvailableNot AvailableNot AvailablePMC9077525
HyphemaNot AvailableNot AvailableNot AvailablePMC9077525
Exposure Sources
Source IDSourceSectorReference
CEDs000399Mydriatics and cycloplegics?Mydriatics and cycloplegics are synthetic chemicals used primarily in ophthalmology to dilate pupils and temporarily paralyze the ciliary muscle, respectively.Healthcare, pharmaceuticals & veterinary productsNot Available
CEDs000511Conductors Or Conductive Bodies Characterised By The Conductive Materials?Conductors, or conductive bodies, are materials that allow the flow of electrical current, typically made from metals such as copper, aluminum, or silver.Electrical & Electronic EquipmentPubChem
CEDs000518Electrically Stimulated Smoking Devices?Electrically stimulated smoking devices, commonly known as e-cigarettes or vape pens, utilize electrical components to heat a liquid solution, often containing nicotine, flavorings, and other additives, to produce an aerosol for inhalation.Electrical & Electronic EquipmentPubChem
CEDs000519Electrodes?Electrodes, used in various electrical and electronic applications, can be a source of synthetic chemical contamination due to the materials from which they are constructed and the processes involved in their manufacturing.Electrical & Electronic EquipmentPubChem
CEDs000556Cigar Cigarettes?Cigar cigarettes are a source of synthetic chemical contamination due to the combustion of various tobacco blends and additives.Household cleaning & consumer productsPubChem
CEDs000560Other Smoking Requisites?Other smoking requisites, including items such as lighters, matches, and rolling papers, can introduce synthetic chemical contamination through various components and additives.Household cleaning & consumer productsPubChem
CEDs000569Tobacco Smoke Filters?Tobacco smoke filters are designed to reduce the inhalation of harmful substances in cigarette smoke, including tar and other particulate matter.Household cleaning & consumer productsPubChem
CEDs000580Manufacture Preparation Of Tobacco Products?The manufacture and preparation of tobacco products involve various processes that can result in the introduction of synthetic chemicals into the environment.Industrial manufacturing & chemical processingPubChem
CEDs000610Aftersun Products?Aftersun products are designed to soothe and hydrate the skin after sun exposure, often containing various synthetic chemicals such as emollients, preservatives, and fragrances.Personal care & cosmeticsPubChem
CEDs000611Anti Perspirants Or Body Deoderants?Antiperspirants and body deodorants commonly contain synthetic chemicals such as aluminum compounds, parabens, and synthetic fragrances.Personal care & cosmeticsPubChem
CEDs000613Depilatories?Depilatories are products designed to remove unwanted hair through the application of synthetic chemicals that break down the protein structure of hair, facilitating its removal.Personal care & cosmeticsPubChem
CEDs000614Essential Oils Or Perfumes?Essential oils and perfumes are complex mixtures of volatile compounds derived from natural or synthetic sources, commonly used for their aromatic properties.Personal care & cosmeticsPubChem
CEDs000615Eye Makeup Products?Eye makeup products, including mascaras, eyeliners, and eyeshadows, often contain a variety of synthetic chemicals such as pigments, preservatives, and film-forming agents.Personal care & cosmeticsPubChem
CEDs000617Lip Care Products?Lip care products, including lipsticks, balms, and glosses, often contain a variety of synthetic chemicals such as parabens, phthalates, and synthetic fragrances.Personal care & cosmeticsPubChem
CEDs000618Lip Makeup Products?Lip makeup products, such as lipsticks, lip glosses, and lip liners, often contain a variety of synthetic chemicals, including pigments, preservatives, and emollients.Personal care & cosmeticsPubChem
CEDs000632Apparel?Apparel production often involves the use of various synthetic chemicals, including dyes, finishing agents, and preservatives.Textiles, leather & furnishingsPubChem
CEDs000685Ceramics?Ceramics can be a source of synthetic chemical contamination through various additives and processing agents used in their production.Building & ConstructionPubChem
CEDs000686Clay Wares?Clay wares are ceramic products made from natural clay, often utilized in various construction applications such as tiles, bricks, and sanitary ware.Building & ConstructionPubChem
CEDs000688Glass Coatings?Glass coatings are synthetic chemical formulations applied to glass surfaces to enhance properties such as durability, UV resistance, and aesthetic appeal.Building & ConstructionPubChem
CEDs000696Nanotechnology?Nanotechnology involves the manipulation of materials at the molecular or atomic level, typically within the range of 1 to 100 nanometers.Industrial manufacturing & chemical processingPubChem
CEDs000734Coating Compositions?Coating compositions, which include paints, sealants, and varnishes, are formulated with a variety of synthetic chemicals such as solvents, resins, pigments, and additives.Building & ConstructionPubChem
CEDs000739Inks?Inks are complex mixtures composed of pigments or dyes, solvents, resins, and additives used primarily for printing and writing applications.Paper, pulp & fiber productsPubChem
Pathways
2 pathwaysPathway Source: PathBank
Targets
StructureProteinUniProt IDOrganismRelationshipDetails
Sodium-dependent noradrenaline transporter structureClick to view 3D structureSodium-dependent noradrenaline transporterP23975HumansPredicted (SEA)
Prediction Confidence Score
0.39
Applicability Domain
0.432
Statistical Significance
0.0062
Supporting Reference Compounds
451
E-value
48.1887
Click to view 3D structureSodium-dependent serotonin transporterP31652Rattus norvegicusPredicted (SEA)
Prediction Confidence Score
0.379
Applicability Domain
0.389
Statistical Significance
0.0082
Supporting Reference Compounds
297
E-value
63.6807
Click to view 3D structureAlpha-1A adrenergic receptorP43140Rattus norvegicusPredicted (SEA)
Prediction Confidence Score
0.379
Applicability Domain
0.389
Statistical Significance
0.0063
Supporting Reference Compounds
208
E-value
49.2007
Sodium-dependent serotonin transporter structureClick to view 3D structureSodium-dependent serotonin transporterP31645HumansPredicted (SEA)
Prediction Confidence Score
0.378
Applicability Domain
0.389
Statistical Significance
0.0141
Supporting Reference Compounds
593
E-value
110.001
Muscarinic acetylcholine receptor M1 structureClick to view 3D structureMuscarinic acetylcholine receptor M1P11229HumansPredicted (SEA)
Prediction Confidence Score
0.374
Applicability Domain
0.432
Statistical Significance
0.0055
Supporting Reference Compounds
385
E-value
42.5057
Muscarinic acetylcholine receptor M2 structureClick to view 3D structureMuscarinic acetylcholine receptor M2P08172HumansPredicted (SEA)
Prediction Confidence Score
0.367
Applicability Domain
0.432
Statistical Significance
0.0047
Supporting Reference Compounds
373
E-value
36.5113
Click to view 3D structureNorepinephrine transporterQ9WTR4Rattus norvegicusPredicted (SEA)
Prediction Confidence Score
0.363
Applicability Domain
0.389
Statistical Significance
0.0036
Supporting Reference Compounds
112
E-value
28.415
Muscarinic acetylcholine receptor M3 structureClick to view 3D structureMuscarinic acetylcholine receptor M3P20309HumansPredicted (SEA)
Prediction Confidence Score
0.355
Applicability Domain
0.432
Statistical Significance
0.005
Supporting Reference Compounds
310
E-value
39.3139
Muscarinic acetylcholine receptor M4 structureClick to view 3D structureMuscarinic acetylcholine receptor M4P08173HumansPredicted (SEA)
Prediction Confidence Score
0.355
Applicability Domain
0.432
Statistical Significance
0.0047
Supporting Reference Compounds
297
E-value
36.8227
Sigma non-opioid intracellular receptor 1 structureClick to view 3D structureSigma non-opioid intracellular receptor 1Q99720HumansPredicted (SEA)
Prediction Confidence Score
0.355
Applicability Domain
0.415
Statistical Significance
0.0242
Supporting Reference Compounds
562
E-value
188.084
Click to view 3D structureTransporterQ63380Rattus norvegicusPredicted (SEA)
Prediction Confidence Score
0.351
Applicability Domain
0.389
Statistical Significance
0.0015
Supporting Reference Compounds
54
E-value
11.5995
Click to view 3D structureSodium-dependent dopamine transporterP23977Rattus norvegicusPredicted (SEA)
Prediction Confidence Score
0.35
Applicability Domain
0.415
Statistical Significance
0.0075
Supporting Reference Compounds
203
E-value
58.6983
5-hydroxytryptamine receptor 2C structureClick to view 3D structure5-hydroxytryptamine receptor 2CP28335HumansPredicted (SEA)
Prediction Confidence Score
0.348
Applicability Domain
0.432
Statistical Significance
0.0261
Supporting Reference Compounds
823
E-value
203.186
5-hydroxytryptamine receptor 2A structureClick to view 3D structure5-hydroxytryptamine receptor 2AP28223HumansPredicted (SEA)
Prediction Confidence Score
0.348
Applicability Domain
0.432
Statistical Significance
0.0354
Supporting Reference Compounds
955
E-value
275.742
Muscarinic acetylcholine receptor M5 structureClick to view 3D structureMuscarinic acetylcholine receptor M5P08912HumansPredicted (SEA)
Prediction Confidence Score
0.342
Applicability Domain
0.432
Statistical Significance
0.0055
Supporting Reference Compounds
266
E-value
42.8949
5-hydroxytryptamine receptor 2B structureClick to view 3D structure5-hydroxytryptamine receptor 2BP41595HumansPredicted (SEA)
Prediction Confidence Score
0.337
Applicability Domain
0.432
Statistical Significance
0.0242
Supporting Reference Compounds
686
E-value
188.551
Voltage-gated inwardly rectifying potassium channel KCNH2 structureClick to view 3D structureVoltage-gated inwardly rectifying potassium channel KCNH2Q12809HumansPredicted (SEA)
Prediction Confidence Score
0.335
Applicability Domain
0.432
Statistical Significance
0.0841
Supporting Reference Compounds
1498
E-value
654.634
Sodium-dependent dopamine transporter structureClick to view 3D structureSodium-dependent dopamine transporterQ01959HumansPredicted (SEA)
Prediction Confidence Score
0.329
Applicability Domain
0.377
Statistical Significance
0.0208
Supporting Reference Compounds
506
E-value
161.926
Histamine H1 receptor structureClick to view 3D structureHistamine H1 receptorP35367HumansPredicted (SEA)
Prediction Confidence Score
0.326
Applicability Domain
0.432
Statistical Significance
0.0288
Supporting Reference Compounds
507
E-value
224.595
Click to view 3D structureMuscarinic acetylcholine receptor M2P10980Rattus norvegicusPredicted (SEA)
Prediction Confidence Score
0.319
Applicability Domain
0.415
Statistical Significance
0.0032
Supporting Reference Compounds
98
E-value
24.6004
Cytochrome P450 2D6 structureClick to view 3D structureCytochrome P450 2D6P10635HumansPredicted (SEA)
Prediction Confidence Score
0.312
Applicability Domain
0.373
Statistical Significance
0.078
Supporting Reference Compounds
1130
E-value
607.302
Click to view 3D structureMuscarinic acetylcholine receptor M1P08482Rattus norvegicusPredicted (SEA)
Prediction Confidence Score
0.312
Applicability Domain
0.415
Statistical Significance
0.0046
Supporting Reference Compounds
109
E-value
35.8885
Click to view 3D structure5-hydroxytryptamine receptor 1AP19327Rattus norvegicusPredicted (SEA)
Prediction Confidence Score
0.306
Applicability Domain
0.377
Statistical Significance
0.0462
Supporting Reference Compounds
541
E-value
359.897
Click to view 3D structurePancreatic alpha-amylaseP00689Rattus norvegicusPredicted (SEA)
Prediction Confidence Score
0.306
Applicability Domain
0.315
Statistical Significance
2.20e-04
Supporting Reference Compounds
2
E-value
1.71268
5-hydroxytryptamine receptor 6 structureClick to view 3D structure5-hydroxytryptamine receptor 6P50406HumansPredicted (SEA)
Prediction Confidence Score
0.306
Applicability Domain
0.373
Statistical Significance
0.0401
Supporting Reference Compounds
536
E-value
311.942
Concentrations
Not Available
External Links
DrugBank IDDB00979
HMDB IDHMDB0015114
FooDB IDNot Available
Phenol Explorer IDNot Available
KNApSAcK IDNot Available
BiGG IDNot Available
BioCyc IDNot Available
METLIN IDNot Available
PDB IDNot Available
Wikipedia LinkCyclopentolate
Chemspider ID2802
ChEBI ID4024
PubChem Compound ID2905
Kegg Compound IDC06932
YMDB IDNot Available
ECMDB IDNot Available
References
Synthesis ReferenceNot Available
MSDSNot Available
General ReferencesNot Available