Description References
ChemicalBook > CAS DataBase List > Furfuryl alcohol

Furfuryl alcohol

Description References
Product Name
Furfuryl alcohol
CAS No.
98-00-0
Chemical Name
Furfuryl alcohol
Synonyms
FA;2-FURANMETHANOL;FURANMETHANOL;FURFURAL ALCOHOL;Furfuranol;2-FURYLMETHANOL;2-furanemethanol;HPFA;2-Furanylmethanol;Furfuryl Alchohol
CBNumber
CB7854741
Molecular Formula
C5H6O2
Formula Weight
98.1
MOL File
98-00-0.mol
More
Less

Furfuryl alcohol Property

Melting point:
-29 °C (lit.)
Boiling point:
170 °C (lit.)
Density 
1.135 g/mL at 25 °C (lit.)
vapor density 
3.4 (vs air)
vapor pressure 
0.5 mm Hg ( 20 °C)
refractive index 
n20/D 1.486(lit.)
FEMA 
2491 | FURFURYL ALCOHOL
Flash point:
149 °F
storage temp. 
Store below +30°C.
solubility 
alcohol: soluble
form 
Liquid
pka
14.02±0.10(Predicted)
color 
Clear yellow
PH
6 (300g/l, H2O, 20℃)
Odor
Mildly irritating.
Odor Threshold
8 ppm
Odor Type
bready
explosive limit
1.8-16.3%(V)
Water Solubility 
MISCIBLE
FreezingPoint 
-29℃
Merck 
14,4305
JECFA Number
451
BRN 
106291
Exposure limits
NIOSH REL: TWA 10 ppm (40 mg/m3), STEL 15 ppm (60 mg/m3), IDLH 75 ppm; OSHA PEL: TWA 50 ppm; ACGIH TLV: TWA 10 ppm, STEL 15 ppm (adopted).
LogP
0.3 at 25℃
CAS DataBase Reference
98-00-0(CAS DataBase Reference)
NIST Chemistry Reference
2-Furanmethanol(98-00-0)
IARC
2B (Vol. 119) 2019
EPA Substance Registry System
2-Furanmethanol (98-00-0)
More
Less

Safety

Hazard Codes 
Xn,T
Risk Statements 
20/21/22-48/20-40-36/37-23-21/22
Safety Statements 
23-36/37/39-63-45-36/37-24/25
RIDADR 
UN 2874 6.1/PG 3
WGK Germany 
1
RTECS 
LU9100000
8
Autoignition Temperature
915 °F
TSCA 
Yes
HS Code 
2932 13 00
HazardClass 
6.1
PackingGroup 
III
Hazardous Substances Data
98-00-0(Hazardous Substances Data)
Toxicity
LC50 (4 hr) in rats: 233 ppm (Jacobson)
IDLA
75 ppm
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H319Causes serious eye irritation

H331Toxic if inhaled

H335May cause respiratory irritation

H351Suspected of causing cancer

H373May cause damage to organs through prolonged or repeated exposure

Precautionary statements

P280Wear protective gloves/protective clothing/eye protection/face protection.

P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

P308+P313IF exposed or concerned: Get medical advice/attention.

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
W249166
Product name
Furfuryl Alcohol
Purity
natural, ≥95%, FG
Packaging
1kg
Price
$135
Updated
2024/03/01
Sigma-Aldrich
Product number
W249166
Product name
Furfuryl Alcohol
Purity
natural, ≥95%, FG
Packaging
10Kg
Price
$805
Updated
2024/03/01
Sigma-Aldrich
Product number
W249166
Product name
Furfuryl Alcohol
Purity
natural, ≥95%, FG
Packaging
25kg
Price
$1880
Updated
2024/03/01
Sigma-Aldrich
Product number
W249106
Product name
Furfuryl Alcohol
Purity
≥97%, FG
Packaging
1kg
Price
$76.5
Updated
2024/03/01
Sigma-Aldrich
Product number
W249106
Product name
Furfuryl Alcohol
Purity
≥97%, FG
Packaging
5kg
Price
$142
Updated
2024/03/01
More
Less

Furfuryl alcohol Chemical Properties,Usage,Production

Description

Furfuryl alcohol is clear colorless organic liquid having a furan substituted with a hydroxymethyl group. It is primarily used for the synthesis of furans resins which are used in thermoset polymer matrix composites, cements, adhesive and coatings. It plays an essential role in the production of foundry sand binder and has long been used to produce cores and molds for metal casting. Other applications include as a fuel and wood treatment. In industry, it is manufactured through either direct reduction of furfural, or through the disproportionation via the Cannizaro reaction in NaOH solution. The basic raw materials for its manufacturing are waste vegetable materials such as rice hulls, sugar cane bagasse, oat hulls or corncobs.

References

https://en.wikipedia.org/wiki/Furfuryl_alcohol
http://www.furan.com/furfuryl_alcohol_applications.html

Description

Furfural alcohol is a colorless to amber liquidthat darkens on exposure to light. It has a faint, burningodor. Molecular weight=98.11; Specific gravityFurfuryl alcohol 1371(H2O:1)=1.13; Boiling point: 171℃; Melting point:215℃; Vapor pressure=6 mmHg at 25℃; Flash point =65℃ (cc); 75℃ (oc); Autoignition temperature=491℃.Explosive limits: LEL=1.8%; UEL=16.3%. HazardIdentification (based on NFPA-704 M Rating System):Health 1, Flammability 2, Reactivity 1. Soluble in water.

Chemical Properties

clear yellow liquid

Chemical Properties

Furfural alcohol is a colorless to amber liquid that darkens on exposure to light. It has a faint, burning odor.

Chemical Properties

Furfuryl alcohol has a very mild, warm, oily, “burnt” odor and a cooked sugar taste.

Physical properties

Clear, colorless to pale yellow liquid with an irritating odor. Darkens to yellowish-brown on exposure to air. A detection odor threshold concentration of 32 mg/m3 (8.0 ppmv) was determined by Jacobson et al. (1958).

Occurrence

Reported found in roasted almonds, cooked apple, apple juice, roasted barley, beans, beef fat, canned beef stew, beer, brandy, white bread, cocoa, cocoa bean, roasted coffee, roasted flberts, honey, heated skim milk, dried mushrooms, roasted onion, yellow passion fruit, roasted peanuts, pineapple, popcorn, potato chips, roasted sesame seeds, cheeses, milk, meats, grape wines, cognac, whiskies, soybean products, coconut, corn oil, shrimps, clams and other sources

Uses

Colorless liquid that turns dark in air

Uses

Furfuryl Alcohol has been obtained by yeast reduction of furfural. Furfuryl Alcohol is used as solvent and in the manufacturing of wetting agents, resins.

Uses

Solvent; manufacture of wetting agents, resins.

Preparation

Usually prepared from furfural that is obtained by the processing of corncobs; oil obtained by steam distillation of roasted coffee bean meal consists of 50% furfuryl alcohol; prepared industrially by the catalytic reduction of furfural using nickel and Cu-CrO catalysts.

Definition

ChEBI: A member of the class of furans bearing a hydroxymethyl substituent at the 2-position.

Aroma threshold values

Detection: 1 to 2 ppm.

Taste threshold values

Taste characteristics at 50 ppm: burnt, sweet, caramellic and brown.

Synthesis Reference(s)

Synthesis, p. 246, 1977
Tetrahedron Letters, 33, p. 5417, 1992 DOI: 10.1016/S0040-4039(00)79109-X

General Description

A clear colorless liquid. Flash point 167°F. Boiling point 171°F. Denser than water. Contact may irritate skin, eyes and mucous membranes. May be toxic by ingestion and skin contact and moderately toxic by inhalation.

Air & Water Reactions

Slightly soluble in water.

Hazard

May react explosively with mineral acids and some organic acids. Toxic by inhalation and skin absorption. Approved for food products. Toxic by skin absorption.

Health Hazard

Inhalation causes headache, nausea, and irritation of nose and throat. Vapor irritates eyes; liquid causes inflammation and corneal opacity. Contact of skin with liquid causes dryness and irritation. Ingestion causes headache, nausea, and irritation of mouth and stomach.

Fire Hazard

Combustible material: may burn but does not ignite readily. When heated, vapors may form explosive mixtures with air: indoors, outdoors and sewers explosion hazards. Contact with metals may evolve flammable hydrogen gas. Containers may explode when heated. Runoff may pollute waterways. Substance may be transported in a molten form.

Chemical Reactivity

Reactivity with Water No reaction; Reactivity with Common Materials: No reactions; Stability During Transport: The product darkens and forms water insoluble material on exposure to air or acids. This reaction is accelerated at elevated temperatures; Neutralizing Agents for Acids and Caustics: Not pertinent; Polymerization: Not pertinent; Inhibitor of Polymerization: Not pertinent.

Biochem/physiol Actions

Taste at 20-40ppm

Safety Profile

Poison by ingestion, skin contact, and subcutaneous routes.Moderately toxic by inhalation and intraperitoneal routes. Mutation data reported. An eye irritant. Flammable when exposed to heat or flame; can react with oxidtzing materials. Moderate explosion hazard when exposed to heat or flame. Reacts violently with acids (e.g., formic acid, cyanoacetic acid + heat). Ignites on contact with 85% hydrogen peroxide. To fight fire, use alcohol foam, CO2, dry chemical. When heated to decomposition it emits acrid smoke and fumes.

Potential Exposure

Used as a starting monomer in the production of furan resins and used to produce tetrahydro furfural alcohol (THFA).

First aid

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.

Carcinogenicity

The NTP conducted a 2-year inhalation study on furfuryl alcohol. F344 rats and B6C3F1 mice were exposed to 0, 2, 8, or 32 ppm furfuryl alcohol for 6 h/day, 5 days/week. All rats exposed to 32 ppm died by week 99; survival of all other animals was similar to control animals. There were increased incidences of nasal tumors in the male rats and increased incidences of kidney tubule tumors in male mice. Increased incidences of nonneoplastic lesions of the nose and increased severities of nephropathy were observed in male and female rats and male mice. Nonneoplastic lesions of nose and corneal degeneration occurred in female mice.

Source

Furfuryl occurs naturally in yarrow, licorice, sesame seeds, clove flowers, and tea leaves (Duke, 1992). Also detected in barrel-aged red, white, and model wines. Concentrations ranged from 3.5 mg/L in white wine after 55 wk of aging to 9.6 mg/L after 11 wk of aging (Spillman et al., 1998). Identified as one of 140 volatile constituents in used soybean oils collected from a processing plant that fried various beef, chicken, and veal products (Takeoka et al., 1996).

Environmental Fate

Biological. In activated sludge inoculum, following a 20-d adaptation period, 97.3% COD removal was achieved. The average rate of biodegradation was 41.0 mg COD/g?h (Pitter, 1976).
Chemical/Physical. Easily resinified by acids (Windholz et al., 1983). Furfuryl alcohol will not hydrolyze because it has no hydrolyzable functional group.
In barrel-aged red, white, and model wines, naturally occurring furfuryl alcohol decreased in concentration with time. In red wine, furfuryl ethyl ether was identified as a degradation product after 55 wk of storage. The average percentage decrease of furfuryl alcohol was 73% (Spillman et al., 1998).

storage

Color Code—Blue: Health Hazard/Poison: Storein a secure poison location. Prior to working with thischemical you should be trained on its proper handling andstorage. Metal containers involving the transfer of=gallonsor more of ethyl acetate should be grounded and bonded.Drums must be equipped with self-closing valves, pressurevacuum bungs, and flame arresters. Use only nonsparkingtools and equipment, especially when opening and closingcontainers of ethyl acetate. Store in containers that are properly labeled with health hazard information and safe handling procedures. Wherever ethyl acetate is used, handled,manufactured, or stored, use explosion-proof electricalequipment and fittings. Furfuryl alcohol must be stored toavoid contact with strong oxidizers (such as chlorine, bromine, and fluorine) and any acid, since violent reactionsoccur. Store in tightly closed containers in a cool, well-ventilated area away from heat. Sources of ignition, such assmoking and open flames, are prohibited where furfurylalcohol is used, handled, or stored in a manner that couldcreate a potential fire or explosion hazard. Wherever furfuryl alcohol is used, handled, manufactured, or stored, useexplosion-proof electrical equipment and fittings.

Shipping

UN2874 Furfuryl alcohol, Hazard Class: 6.1; Labels: 6.1-Poisonous materials.

Purification Methods

Distil it under reduced pressure to remove tarry material, shake with aqueous NaHCO3, dry it with Na2SO4 and fractionally distil it under reduced pressure from Na2CO3. It can be further dried by shaking with Linde 5A molecular sieves. [Beilstein 17/3 V 338.]

Incompatibilities

Incompatible with oxidizers (chlorates, nitrates, peroxides, permanganates, perchlorates, chlorine, bromine, fluorine, etc.); contact may cause fires or explo sions. Keep away from alkaline materials, strong bases, strong acids, oxoacids, epoxides. Contact with acids can cause polymerization. Strong reaction with oxidizers. Incompatible with alkaline earth and alkali metals; strong caustics; aliphatic amines; isocyanates, acetaldehyde, benzoyl peroxide; chromic acid, chromium trioxide; cyanoacetic acid; dialkylzincs, dichlorine oxide; ethylene oxide; hydrogen per oxide; isopropyl chlorocarbonate; lithium tetrahydroalumi nate; nitric acid; nitrogen dioxide; pentafluoroguanidine, phosphorus pentasulfide; tangerine oil; triethylaluminum, trii sobutylaluminum. Attacks some plastics, coatings and rubber.

Waste Disposal

Incineration in admixture with a more flammable solvent.

More
Less

Furfuryl alcohol Suppliers

Changxin Chemical Science-Tech Co., Ltd.
Tel
18006408869
Email
cxyx@sdcxchem.com
Country
China
ProdList
5
Advantage
58
Shandong chuangying chemical co., ltd
Tel
155-8990-1131; 15589901131
Email
2235633711@qq.com
Country
China
ProdList
162
Advantage
58
Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
4006608290; 18621169109
Fax
86-21-61259102
Email
market03@meryer.com
Country
China
ProdList
40241
Advantage
62
Alfa Aesar
Tel
400-6106006
Fax
021-67582001/03/05
Email
saleschina@alfa-asia.com
Country
China
ProdList
30132
Advantage
84
TCI (Shanghai) Development Co., Ltd.
Tel
021-67121386
Fax
021-67121385
Email
Sales-CN@TCIchemicals.com
Country
China
ProdList
24539
Advantage
81
ShangHai DEMO Chemical Co.,Ltd
Tel
400-021-7337 2355568890
Fax
0086-21-50182339
Email
sales@demochem.com
Country
China
ProdList
2572
Advantage
57
Energy Chemical
Tel
021-021-58432009 400-005-6266
Fax
021-58436166
Email
sales8178@energy-chemical.com
Country
China
ProdList
44751
Advantage
61
Capot Chemical Co., Ltd
Tel
+86 (0) 571 85 58 67 18
Fax
0086-571-85864795
Email
sales@capotchem.com
Country
China
ProdList
18217
Advantage
66
Beijing Ouhe Technology Co., Ltd
Tel
010-82967028 13552068683
Fax
+86-10-82967029
Email
2355560935@qq.com
Country
China
ProdList
12426
Advantage
60
Shanghai Hanhong Scientific Co.,Ltd.
Tel
021-54306202 13764082696;
Email
info@hanhongsci.com
Country
China
ProdList
42982
Advantage
64
Chemsky(shanghai)International Co.,Ltd.
Tel
021-50135380
Email
shchemsky@sina.com
Country
China
ProdList
32344
Advantage
50
jiliang chemicals
Tel
21-62165282 15801962796;
Fax
021 61153784
Email
bidingchem@163.com
Country
China
ProdList
1165
Advantage
60
Shandong Xiya Chemical Co., Ltd
Tel
13355009207 13355009207
Fax
0539-6365991
Email
3007715519@qq.com
Country
China
ProdList
18739
Advantage
57
Syntechem Co.,Ltd
Tel
Fax
E-Mail Inquiry
Email
info@syntechem.com
Country
China
ProdList
12990
Advantage
57
BEST-REAGENT
Tel
400-1166-196 18981987031
Fax
028-84555506 800101999
Email
cdhxsj@163.com
Country
China
ProdList
11726
Advantage
57
Sinopharm Chemical Reagent Co,Ltd.
Tel
86-21-63210123
Fax
86-21-63290778 86-21-63218885
Email
sj_scrc@sinopharm.com
Country
China
ProdList
9823
Advantage
79
Maya High Purity Chemicals
Tel
+86 (573) 82222445 (0)18006601000 452520369
Fax
+86 (573) 82222643
Email
sales@maya-r.com
Country
China
ProdList
11714
Advantage
57
Spectrum Chemical Manufacturing Corp.
Tel
021-021-021-67601398-809-809-809 15221380277
Fax
021-57711696
Email
marketing_china@spectrumchemical.com
Country
China
ProdList
9664
Advantage
60
Chengdu Ai Keda Chemical Technology Co., Ltd.
Tel
4008-755-333 18080918076
Fax
028-86757656
Email
800078821@qq.com
Country
China
ProdList
9725
Advantage
55
Qingdao Free Trade Zone United International Co.,Ltd.
Tel
0532-83893697 18561902820
Fax
83893695
Email
sissili@unitedint.com
Country
China
ProdList
352
Advantage
58
Shanghai civi chemical technology co.,Ltd
Tel
86-21-34053660
Fax
86-21-34053661
Email
sale@labgogo.com
Country
China
ProdList
9872
Advantage
52
Thermo Fisher Scientific
Tel
800-810-5118
Fax
+86-10-84193589
Email
cnchemical@thermofisher.com
Country
China
ProdList
17779
Advantage
75
Beijing innoChem Science & Technology Co.,Ltd.
Tel
400-810-7969 010-59572699
Fax
010-59572688
Email
ningzi.li@inno-chem.com.cn
Country
China
ProdList
6139
Advantage
55
Shanghai T&W Pharmaceutical Co., Ltd.
Tel
+86 21 61551611
Fax
+86 21 50676805
Country
China
ProdList
9901
Advantage
58
9ding chemical ( Shanghai) Limited
Tel
4009209199
Fax
86-021-52271987
Email
sales@9dingchem.com
Country
China
ProdList
22519
Advantage
55
Shanghai Aladdin Bio-Chem Technology Co.,LTD
Tel
400-6206333 18521732826;
Fax
021-50323701
Email
market@aladdin-e.com
Country
China
ProdList
25015
Advantage
65
The future of Shanghai Industrial Co., Ltd.
Tel
021-61552785
Fax
021-55660885
Email
sales@shshiji.com
Country
China
ProdList
9552
Advantage
55
Shanghai Tauto Biotech Co., Ltd.
Tel
021-51320588
Fax
0086-21-51320502
Email
tauto@tautobiotech.com
Country
China
ProdList
3989
Advantage
66
Zouping Mingxing Chemical Co.,Ltd.
Tel
86-13605431940 13605431940
Fax
0086-0543-2240079
Email
zpmxchemical@126.com
Country
China
ProdList
2002
Advantage
62
Wuxi Zhangkun Biochemical Technology Co., Ltd.
Tel
+86 0510-85629785
Fax
+86 0510-85625359
Country
China
ProdList
2331
Advantage
58
Shandong Xinhua Pharmceutical Co.,LTD
Tel
0533-2196801
Fax
0533-2196817
Email
yaojianyong@xhzy.com
Country
China
ProdList
70
Advantage
60
Vientiane Tianjin Hengyuan Technology Co., Ltd.
Tel
15722085254
Fax
022-26358246
Email
phytochemical@126.com
Country
China
ProdList
813
Advantage
55
Chengdu HuaXia Chemical Reagent Co. Ltd
Tel
400-1166-196 13458535857
Fax
QQ:800101999
Email
cdhxsj@163.com
Country
China
ProdList
13358
Advantage
58
Wuxi Zhongkun Biochemical Technology Co., Ltd.
Tel
0510-85629785 18013409632
Fax
051085625359
Email
sales@reading-chemicals.com
Country
China
ProdList
15185
Advantage
58
Wuhan Dahua Pharmaceutical Co., Ltd.
Tel
027-59262863 13277907145 3091977954
Fax
027-59420980
Country
China
ProdList
4951
Advantage
58
Shanghai YuLue Chemical Co., Ltd.
Tel
021-60345187 13671753212
Fax
021-34702061
Email
lzz841106@aliyun.com
Country
China
ProdList
10287
Advantage
55
Shanghai Macklin Biochemical Co.,Ltd.
Tel
15221275939 15221275939
Fax
021-50706099
Email
shenlinxing@macklin.cn
Country
China
ProdList
15878
Advantage
55
Shanghai Kewel Chemical Co., Ltd.
Tel
021-64609169 18901607656
Fax
021-64609160
Email
greensnown@163.com
Country
China
ProdList
9911
Advantage
50
SHANGHAI BANGCHENG CHEMICAL Co.,Ltd.
Tel
021-69106960 13701823733
Fax
021-69106780
Email
13701823733@163.com
Country
China
ProdList
4775
Advantage
60
Shanghai YouPeng Chemical Co. Ltd.
Tel
021-69005955 13701776567
Fax
021-69005775
Email
youpengchem@163.com
Country
China
ProdList
4303
Advantage
56
Shanghai TongYuan Chemical Co., Ltd.
Tel
021-021-69182866 13701855675
Fax
021-69182022
Email
tongyuanchem@126.com
Country
China
ProdList
4331
Advantage
58
Shanghai Kaisai Chemical Co., Ltd
Tel
021-33516722 13701817765
Fax
021-33516776
Email
kaisaichem@163.com
Country
China
ProdList
4751
Advantage
58
Chengdu RunZeBenTu Chemical Co., Ltd
Tel
13096311329 028-88469284 616445927
Fax
028-88469284
Email
616445927@qq.com
Country
China
ProdList
2876
Advantage
50
Shanghai LanRun Chemical Co., Ltd.
Tel
021-69515658 ; 69515628 13701998368
Fax
021-69515998
Email
longrunchem@163.com
Country
China
ProdList
3920
Advantage
50
Shanghai Rolead Chemical Technology Co., Ltd.
Tel
021-69992220 13701886816
Fax
021-69992237
Email
roleadchem@163.com
Country
China
ProdList
4759
Advantage
50
Shanghai Kangtuo Chemical Co., Ltd.
Tel
021-69185552 13701777608
Fax
021-69186006
Email
kangtuochem@163.com
Country
China
ProdList
4369
Advantage
55
Chizhou Kailong Import and Export Trade Co., Ltd.
Tel
Fax
-
Email
xg01_gj@163.com
Country
China
ProdList
9503
Advantage
50
Changsha Jing Kang New Material Technology Co., Ltd.
Tel
0731-85118349 18874718518
Fax
0731-85118349
Email
ma_haihong@sina.com
Country
China
ProdList
1597
Advantage
50
Sigma-Aldrich
Tel
021-61415566 800-8193336
Email
orderCN@merckgroup.com
Country
China
ProdList
51471
Advantage
80
Zhengzhou KeYulong chemical products Co., Ltd
Tel
17319789407
Fax
0371-53335504
Email
Keyulongchem@163.com
Country
China
ProdList
1993
Advantage
55
More
Less

View Lastest Price from Furfuryl alcohol manufacturers

Guangzhou PI PI BIOTECH INC
Product
Furosemide Impurity 5
Price
US $0.00-0.00/mg
Min. Order
10mg
Purity
90%+
Supply Ability
10g
Release date
2020-05-31
Hebei Mojin Biotechnology Co., Ltd
Product
Furfuryl alcohol 98-00-0
Price
US $0.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
50000KG/month
Release date
2023-08-18
Hebei Guanlang Biotechnology Co,.LTD
Product
2-(Hydroxymethyl)Furan 98-00-0
Price
US $10.50/KG
Min. Order
1KG
Purity
99%
Supply Ability
10 ton
Release date
2021-07-01

98-00-0, Furfuryl alcoholRelated Search:


  • (2-furyl)-methano
  • 2-furanemethanol
  • 2-Furanmethanol (furfuryl alcohol)
  • 2-Furanylmethanol
  • 2-Furfurylalkohol
  • 2-furfurylalkohol(czech)
  • 2-Hydroxymethyklfuran
  • 2-hydroxymethylfurane
  • 5-Hydroxymethylfuran
  • 5-Hydroxymethylfuranal
  • alcoolfurfurylique
  • alpha-Furfuryl alcohol
  • alpha-furfurylalcohol
  • Furan-2-yl-methanol
  • furfuryl alcohol (furfurol)
  • Furyl alcohol
  • furylalcohol
  • Furylcarbinol
  • Methanol, (2-furyl)-
  • FURAN-2-METHANOL
  • FEMA 2491
  • FA(R)
  • FA
  • FURFURYL ALCOHOL 98+%
  • FurfurylAlcoholForSynthesis
  • FurfurylAlcohol,>99%
  • Furfurylalcohol,98%min
  • TIMTEC-BB SBB004373
  • RARECHEM AL BD 0007
  • furfurylalcohol,2-hydroxymethylfuran
  • Pyr-2-ylmethanol
  • 2-FURYLALCOHOL
  • FURANMETHANOL
  • Furfurylalkohol
  • 2-furfurylalkoho
  • furfralcohol
  • FURFURYL ALCOHOL WITH GC
  • (Fur-2-yl)methanol, Furfuryl alcohol
  • Furfuryl alcohol, 98% 1LT
  • Furfuryl alcohol, 98% 250ML
  • NCI-C56224
  • Qo furfuryl alcohol
  • ALPHA-FURYLCARBINOL
  • AKOS BBS-00004319
  • A-FURYLCARBINOL
  • 2-(HYDROXYMETHYL)FURAN
  • 2-FURYLMETHANOL
  • 2-FURFURYLALCOHOL
  • 2-FURANMETHANOL
  • 2-FURYLCARBINOL
  • 2-FURANCARBINOL
  • LABOTEST-BB LT01986403
  • HPFA
  • FURFURYL ALCOHOL
  • FURFURAL ALCOHOL
  • FURFURALCOHOL
  • 2-FurylMethyl Alcohol
  • CheM-Rez 200