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Tetrahydrofurfuryl alcohol
Tetrahydrofurfuryl alcohol

Tetrahydrofurfuryl alcohol

Price USD1.00
Packge 1IU
  • Min. Order:1KG
  • Supply Ability:100kg
  • Time:2019-12-29

Product Details

  • Product NameTetrahydrofurfuryl alcohol
  • CAS No.97-99-4
  • EINECS No.202-625-6
  • MFC5H10O2
  • MW102.13
  • InChIKeyBSYVTEYKTMYBMK-UHFFFAOYSA-N
  • AppearanceLiquidClear
  • Water Solubility soluble
  • Melting point -80 °C (lit.)
  • density 1.054 g/mL at 25 °C (lit.)
  • Boiling point 178 °C (lit.)
  • storage temp. Store below +30°C.
Synonyms:
tetrahydro-furfurylalcoho;Tetrahydrofurfurylalkohol;Tetrahydrofuryl carbinol;Tetrahydrofurylalkohol;tetrahydrofurylalkohol(czech);tetrahydrofurylcarbinol;TETRAHYDROFURFURYL ALCOHOL, 98%TETRAHYDROFURFURYL ALCOHOL, 98%TETRAHYDROFURFURYL ALCOHOL, 98%;Tetrahydrofurylmethanol
CAS:
MF:
C5H10O2
MW:
102.13
EINECS:
202-625-6
Mol File:
Tetrahydrofurfuryl alcohol Structure
 
Tetrahydrofurfuryl alcohol Chemical Properties
Melting point 
-80 °C
Boiling point 
178 °C(lit.)
density 
1.0543
vapor density 
3.52 (vs air)
vapor pressure 
2.3 mm Hg ( 39 °C)
refractive index 
n20/D 1.452(lit.)
Fp 
183 °F
storage temp. 
Store below +30°C.
solubility 
acetone: miscible(lit.)
pka
14.44±0.10(Predicted)
form 
Liquid
color 
Clear
explosive limit
1.5-9.7%(V)
Water Solubility 
soluble
Sensitive 
Hygroscopic
JECFA Number
1443
Merck 
14,9213
BRN 
102723
InChIKey
BSYVTEYKTMYBMK-UHFFFAOYSA-N
CAS DataBase Reference
NIST Chemistry Reference
EPA Substance Registry System
 
Safety Information
Hazard Codes 
Risk Statements 
Safety Statements 
RIDADR 
NA 1993 / PGIII
WGK Germany 
2
RTECS 
LU2450000
Autoignition Temperature
282 °C
TSCA 
Yes
HS Code 
29321300
Hazardous Substances Data
Toxicity
LD50 orally in Rabbit: 1600 mg/kg
MSDS Information
Provider
Language
English
English
English
English
 
Tetrahydrofurfuryl alcohol Usage And Synthesis
Chemical Properties
Colorless to light yellow liqui
Chemical Properties
Tetrahydrofurfuryl alcohol has a faint, warm, oily, caramellic odor with a coffee and nut-like flavor at very low levels (0.03 to 1 ppm).
Occurrence
Reported found in shoyu (fermented soya hydrolysate), coffee and fresh mango.
Uses
Solvent for vinyl resins; dyes for leather; chlorinated rubber; cellulose esters; solvent softener for nylon; vegetable oils; coupling agent; organic synthesis.
Preparation
By catalytic reduction of furfural with Raney-Ni; also by destructive hydrogenation of lignin.
General Description
A clear colorless liquid with a mild odor. Flash point 167°F. Vapors are heavier than air.
Air & Water Reactions
Denser than water and soluble in water.
Reactivity Profile
Acetyl bromide reacts violently with alcohols or water [Merck 11th ed. 1989]. Mixtures of alcohols with concentrated sulfuric acid and strong hydrogen peroxide can cause explosions. Example: An explosion will occur if dimethylbenzylcarbinol is added to 90% hydrogen peroxide then acidified with concentrated sulfuric acid. Mixtures of ethyl alcohol with concentrated hydrogen peroxide form powerful explosives. Mixtures of hydrogen peroxide and 1-phenyl-2-methyl propyl alcohol tend to explode if acidified with 70% sulfuric acid [Chem. Eng. News 45(43):73. 1967; J, Org. Chem. 28:1893. 1963]. Alkyl hypochlorites are violently explosive. They are readily obtained by reacting hypochlorous acid and alcohols either in aqueous solution or mixed aqueous- carbon tetrachloride solutions. Chlorine plus alcohols would similarly yield alkyl hypochlorites. They decompose in the cold and explode on exposure to sunlight or heat. Tertiary hypochlorites are less unstable than secondary or primary hypochlorites [NFPA 491 M 1991]. Base-catalysed reactions of isocyanates with alcohols should be carried out in inert solvents. Such reactions in the absence of solvents often occur with explosive violence [Wischmeyer 1969].
Health Hazard
Inhalation or contact with material may irritate or burn skin and eyes. Fire may produce irritating, corrosive and/or toxic gases. Vapors may cause dizziness or suffocation. Runoff from fire control or dilution water may cause pollution.
Carcinogenicity
Tetrahydro-2-furanmethanol was not mutagenic to S. typhimurium strains TA100, TA1535, TA1537, or TA98 in an in vitro gene mutation assay or to E. coliWP2uvrA/pKM101 with or withoutmetabolic activation. No chromosomal aberrations or polypoidy were observed when tetrahydro-2-furanmethanol was added to cultured Chinese hamster lung cells with or without metabolic activation .
 

Company Profile Introduction

Established in 2014,Career Henan Chemical Co. is a manufacturerspecializing in the sale of fine chemicals. Mainly deals in the sales of: Pharmaceutical intermediates OLED intermediates: Pharmaceutical intermediates; OLED intermediates;
  • Since:2014-12-17
  • Address: Room 702, Floor 7, Building 10, National University Science Park, High-Tech Zone, Zhengzhou City, H
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