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1-Pentanol

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Products Intro: Product Name:1-Pentanol
CAS:71-41-0
Purity:99% Package:25KG
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Products Intro: Product Name:1-Pentanol
CAS:71-41-0
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Products Intro: Product Name:1-Pentanol
CAS:71-41-0
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Products Intro: Product Name:1-Pentanol
CAS:71-41-0
Purity:99.5 Package:1ASSAYS;1USD

1-Pentanol manufacturers

  • 1-Pentanol
  • 1-Pentanol pictures
  • $0.00 / 200KG
  • 2023-09-06
  • CAS:71-41-0
  • Min. Order: 1KG
  • Purity: 99%
  • Supply Ability: 500000kg
  • 1-Pentanol
  • 1-Pentanol pictures
  • $1.50 / 1g
  • 2023-07-27
  • CAS:71-41-0
  • Min. Order: 1g
  • Purity: 99.0% Min
  • Supply Ability: 100 Tons
  • 1-Pentanol
  • 1-Pentanol pictures
  • $0.00 / 25KG
  • 2023-06-20
  • CAS:71-41-0
  • Min. Order: 1KG
  • Purity: 99%
  • Supply Ability: 50000KG/month
1-Pentanol Basic information
Product Name:1-Pentanol
Synonyms:1-Pentanol ACS reagent, >=99%;1-Pentanol puriss. p.a., ACS reagent, >=99.0% (GC);1-Pentanol ReagentPlus(R), >=99%;1-Pentanol, ACS, 99.0% min.;Amyl Alcohol Butylcarbinol Pentan-1-ol n-Amyl alcohol Pentyl alcohol;n-Amyl alcohol (Pentan-1-ol) for analysis EMSURE;Alcool amylique;primaryamylalcohol
CAS:71-41-0
MF:C5H12O
MW:88.15
EINECS:200-752-1
Product Categories:ACS and Reagent Grade Solvents;ACS Grade Solvents;Analytical Reagents;Lavandula angustifolia (Lavendar tea);Biochemicals and Reagents;Carbon Steel Flex-Spout Cans;Carthamus tinctorius (Safflower oil);Citrus aurantium (Seville orange);Fatty Acyls;Fatty Alcohols;Lipids;Nutrition Research;Phytochemicals by Plant (Food/Spice/Herb);ReagentPlus;Semi-Bulk Solvents;Solvent Packaging Options;Solvents;Analytical Reagents for General Use;Analytical/Chromatography;O-P;Puriss p.a. ACS;Solvent by Application;1-Alkanols;Monofunctional & alpha,omega-Bifunctional Alkanes;Monofunctional Alkanes;K00001
Mol File:71-41-0.mol
1-Pentanol Structure
1-Pentanol Chemical Properties
Melting point -78 °C (lit.)
Boiling point 136-138 °C (lit.)
density 0.811 g/mL at 25 °C (lit.)
vapor density 3 (vs air)
vapor pressure 1 mm Hg ( 13.6 °C)
FEMA 2056 | AMYL ALCOHOL
refractive index n20/D 1.409(lit.)
Fp 120 °F
storage temp. Store below +30°C.
solubility water: soluble22.8g/L at 25°C
form Liquid
pka15.24±0.10(Predicted)
color APHA: ≤30
Relative polarity0.568
PH Range7
OdorPleasant 0.1 ppm
Odor Typefermented
Odor Threshold0.1ppm
explosive limit10%, 100°F
Water Solubility 22 g/L (22 ºC)
Merck 14,7118
JECFA Number88
BRN 1730975
Dielectric constant15.8(20℃)
Stability:Stable. Flammable. Incompatible with strong oxidizing agents.
LogP1.51
CAS DataBase Reference71-41-0(CAS DataBase Reference)
NIST Chemistry Reference1-Pentanol(71-41-0)
EPA Substance Registry System1-Pentanol (71-41-0)
Safety Information
Hazard Codes Xn,F,Xi
Risk Statements 10-20-37-66-37/38
Safety Statements 46-36/37
RIDADR UN 1105 3/PG 3
WGK Germany 1
RTECS SB9800000
Autoignition Temperature572 °F
Hazard Note Irritant/Flammable
TSCA Yes
HS Code 2905 19 00
HazardClass 3
PackingGroup II
Hazardous Substances Data71-41-0(Hazardous Substances Data)
ToxicityLD50 orally in Rabbit: 3670 mg/kg LD50 dermal Rabbit 2306 mg/kg
MSDS Information
ProviderLanguage
ACROS English
SigmaAldrich English
ALFA English
1-Pentanol Usage And Synthesis
Description1-Pentanol is a monohydroxy alcohol. It is a colorless liquid with a characteristic odor. Its combustion properties have been studied as it shows promising features to be an alternative to gasoline and diesel fuels. The conversion of 1-pentanol to di-n-pentyl ether (DNPE) in liquid phase at 423K in a batch reactor using ion exchange resins as catalysts.
Chemical Properties1-Pentanol is a clear, colorless liquid at ambient temperatures.The air odor detection level (lowest perceptible level) was reported as 10 ppm for 1-pentanol .
Chemical PropertiesAmyl alcohols (pentanols) have eight isomers. All are flammable, colorless liquids, except the isomer 2,2- dimethyl-1-propanol, which is a crystalline solid.
Amyl alcohol has a characteristic fusel-like sweet and pleasant odor and burning taste. It is somewhat more toxic than ethyl alcohol.
OccurrenceReported found in banana, sweet cherry, cranberry, bourbon, vanilla, rice bran and Brazil nut.
UsesRaw material for pharmaceutical preparations;organic synthesis solvent.
1-Pentanol is used as a key starting material in the production of dichloro-acetic acid pentyl ester, 2-methyltetrahydrofuran, di-n-penyl ether (DNPE), pentyl butyrate and amyl acetate. As a solvent, it is used for coating CDs and DVDs. It has been considered to be a replacement for gasoline and diesel fuels due to its combustion properties. Further, it is used as a reagent to prepare derivatives of ferulic acid and caffeic acid, which shows anticancer properties.
Uses1-Pentanol may be used as a cosurfactant in the water-in-oil mixed surfactant microemulsions.
Production Methods1-Pentanol is made primarily by the oxo process, which involves the reaction of butenes with carbon monoxide and hydrogen in the presence of a catalyst, followed by hydrogenation. 1-Pentanol is used as a solvent, as a chemical intermediate for esters, and as a food additive and flavoring substance. The primary routes of industrial exposure are by dermal contact and inhalation.
DefinitionChEBI: An alkyl alcohol that is pentane in which a hydrogen of one of the methyl groups is substituted by a hydroxy group. It has been isolated from Melicope ptelefolia.
Aroma threshold valuesDetection at 1.6 to 70 ppm
Taste threshold valuesTaste characteristics at 50 ppm: intense fusel, fermented, bready and cereal with a fruity undertone
General DescriptionA colorless liquid with a mild to moderately strong odor. Less dense than water. Flash point 91°F. Boiling point 280°F. Vapors heavier than air. Moderately toxic by ingestion. Vapors may irritate skin and eyes. Used as a solvent and to make other chemicals.
Pentanol is incompatible with strong oxidising agents, alkali metals, alkaline earth metals, halogens, hydrogen trisulphide, acids, acetaldehyde, acid anhydrides, acid chlorides, lithium aluminium hydride, isocyanates, dialkylmagnesiums, n-halomides, ethylene oxide, hypochlorous acid, hydrogen peroxide and sulphuric acid, nitrogen tetraoxide, nitryl hypochlorite, permonosulphuric acid, and tri-isobutyl aluminium.
Air & Water ReactionsHighly flammable. Soluble in water.
Reactivity ProfileModerately toxic, flammable if exposed to powerful oxidizers. Incompatible with oxidizing materials, hydrogen trisulfide [Sax, 9th ed., 1996, p. 224].
HazardLower explosive level in air 1.2% by volume. Moderate fire risk.
Health HazardIrritation of skin, eyes, and respiratory tract; headache and vertigo; dyspnea and cough; nausea, vomiting, and diarrhea. Double vision, deafness, delirium, and occasionally fatal poisoning, preceded by severe nervous symptoms, have been reported. Coma, glycosuria, and methemoglobinemia can occur.
Fire HazardHIGHLY FLAMMABLE: Will be easily ignited by heat, sparks or flames. Vapors may form explosive mixtures with air. Vapors may travel to source of ignition and flash back. Most vapors are heavier than air. They will spread along ground and collect in low or confined areas (sewers, basements, tanks). Vapor explosion hazard indoors, outdoors or in sewers. Runoff to sewer may create fire or explosion hazard. Containers may explode when heated. Many liquids are lighter than water.
Safety ProfileModerately toxic by ingestion and skin contact. An eye and upper respiratory irritant by inhalation. A severe skin and eye irritant. Ingestion can cause headache, nausea, vomiting, delirium, and methemoglobin formation. Mutation data reported. Extremely flammable if exposed to heat, flame, or powerful oxiduers. Moderately explosive when exposed to flame. Incompatible with oxidzing materials, hydrogen trisulfide. To fight fire, use alcohol foam, dry chemical.
Potential Exposure(n-isomer); Suspected reprotoxic hazard, Primary irritant (w/o allergic reaction), (iso-, primary): Possible risk of forming tumors, Primary irritant (w/o allergic reaction), (sec-, active primary-, and other isomers) Primary irritant (w/o allergic reaction). Used as a solvent in organic synthesis and synthetic flavoring, pharmaceuticals, corrosion inhibitors; making plastics and other chemicals; as a flotation agent. The (n-isomer) is used in preparation of oil additives, plasticizers, synthetic lubricants, and as a solvent.
First aidSkin contact contributes significantly to overallexposure. If this chemical gets into the eyes, remove anycontact lenses at once and irrigate immediately for at least15 min, occasionally lifting upper and lower lids. Seek medical attention immediately. If this chemical contacts theskin, remove contaminated clothing and wash immediatelywith soap and water. Seek medical attention immediately. Ifthis chemical has been inhaled, remove from exposure,begin rescue breathing (using universal precautions, including resuscitation mask) if breathing has stopped and CPR ifheart action has stopped. Transfer promptly to a medicalfacility. When this chemical has been swallowed, get medical attention. Give large quantities of water and inducevomiting. Do not make an unconscious person vomit.
storageColor Code—Red: Flammability Hazard: Store ina flammable liquid storage area or approved cabinet awayfrom ignition sources and corrosive and reactive materials.Prior to working with this chemical you should be trained onits proper handling and storage. Before entering confinedspace where amyl alcohols may be present, check to makesure that an explosive concentration does not exist. Store intightly closed containers in a cool, well-ventilated area awayfrom strong oxidizers; strong acids and hydrogen trifluoride;since violent reactions occur. Metal containers involving thetransfer of this chemical should be grounded and bonded.Where possible, automatically pump liquid from drums orother storage containers to process containers. Drums mustbe equipped with self-closing valves, pressure vacuumbungs; and flame arresters. Use only nonsparking tools andequipment, especially when opening and closing containersof this chemical. Sources of ignition, such as smoking andopen flames, are prohibited where this chemical is used,handled, or stored in a manner that could create a potentialfire or explosion hazard.
ShippingUN2811 Pentanols, Hazard Class: 3; Labels: 3- Flammable liquid. UN1987 Alcohols, n.o.s., Hazard Class: 3; Labels: 3-Flammable liquid.
Purification MethodsDry 1-pentanol with anhydrous K2CO3 or CaSO4, filter and fractionally distil it. It has also been treated with 1-2% of sodium and heated at reflux for 15hours to remove water and chlorides. Traces of water can be removed from the near-dry alcohol by refluxing it with a small amount of sodium in the presence of 2-3% n-amyl phthalate or succinate followed by distillation (see ethanol). Small amounts of amyl alcohol have been purified by esterifying with p-hydroxybenzoic acid, recrystallising the ester from CS2, saponifying with ethanolic-KOH, drying with CaSO4 and fractionally distilling [Olivier Recl Trav Chim Pays-Bas 55 1027 1936]. [Beilstein 1 IV 1640.]
IncompatibilitiesForms an explosive mixture with air. Contact with strong oxidizers and hydrogen trisulfide may cause fire and explosions. Incompatible with strong acids. Violent reaction with alkaline earth metals forming hydrogen, a flammable gas.
Waste DisposalDissolve or mix the material with a combustible solvent and burn in a chemical incinerator equipped with an afterburner and scrubber. All federal, state, and local environmental regulations must be observed.
Tag:1-Pentanol(71-41-0) Related Product Information
5-Amino-1-pentanol Tebuconazole Ethyl acetate Dipentaerythritol 2-Methyl-2-butanol Isoamyl nitrite 4-Methyl-1-pentanol Pentaerythritol triacrylate Rosin pentaerythrityl ester 5-Bromopentan-1-ol Potassium Amylxanthate Amylamine N-OCTANE Valeronitrile Valeric acid Pentane Valeraldehyde PENTYL VALERATE Amyl Alcohol