1,8-Octanediol supplier | CasNO.629-41-4

Name
Octane-1,8-diol
EINECS 211-090-8
CAS No. 629-41-4
Article Data87
CAS DataBase
Density 0.939 g/cm³
Solubility Soluble in water and methanol.
Melting Point 57-61 °C(lit.)
Formula C₈H₁₈O₂
Boiling Point 278.8 °C at 760 mmHg
Molecular Weight 146.23
Flash Point 128 °C
Transport Information
Appearance colorless to white crystals or flakes
Safety 26-37/39
Risk Codes 20/21/22-36/37/38
Molecular Structure
Hazard Symbols Xn, Xi
Synonyms Octane-1,8-diol;18-Octanediol;1,8-Octandiol;
PSA 40.46000
LogP 1.31160

Synthetic route

: 1,8-bis(benzyloxy)octane

: 629-41-4
1,8-Octanediol

Conditions

Conditions	Yield
With Pd(OH)2/C In methanol for 5h; Reflux;	96%

: 51326-52-4
8-(tetrahydro-2H-pyran-2-yloxy)octan-1-ol

: 629-41-4
1,8-Octanediol

Conditions

Conditions	Yield
With tin(ll) chloride In methanol Substitution;	95%
With cerium(III) chloride In methanol at 20℃; for 2h; detetrahydropyranylation;	90%

: 91898-31-6
tert-Butyl-[8-(2-methoxy-ethoxymethoxy)-octyloxy]-dimethyl-silane

: 629-41-4
1,8-Octanediol

Conditions

Conditions	Yield
With cerium(III) chloride In acetonitrile for 1h; Heating;	92%

: 69891-87-8
1,8-di(2-terahydropyranyloxy)-octane

: 629-41-4
1,8-Octanediol

Conditions

Conditions	Yield
With toluene-4-sulfonic acid In methanol; water for 8h; Heating;	89%

: 871-84-1
1,7-Octadiyne

: 629-41-4
1,8-Octanediol

Conditions

Conditions	Yield
With formic acid; F6P(1-)*C16H22N3Ru(1+); water In 1-methyl-pyrrolidin-2-one at 25℃; for 24h; Inert atmosphere; Sealed tube;	89%
With 1-hydroxytetraphenylcyclopentadienyl(tetraphenyl-2,4-cyclopentadien-1-one)-μ-hydrotetracarbonyldiruthenium(II); Ru(Cp)(PPh2PytBu)2(MeCN)PF6; water In isopropyl alcohol at 80℃; for 3h; Inert atmosphere; regioselective reaction;	80%

: 50816-19-8
8-bromooctanol

A: 629-41-4
1,8-Octanediol

B: 22054-14-4
8-hydroxyoctanal

Conditions

Conditions	Yield
With 4-methylmorpholine N-oxide In dimethyl sulfoxide at 20℃; for 65.5h;	A 26% B 83%

: 2050-23-9
diethyl suberate

: 629-41-4
1,8-Octanediol

Conditions

Conditions	Yield
With lithium aluminium tetrahydride	81%
With copper chromite at 250℃; under 308913 Torr; Hydrogenation;
With ethanol; sodium
With lithium aluminium tetrahydride; diethyl ether

: 91898-33-8
tert-Butyl-(8-methoxymethoxy-octyloxy)-dimethyl-silane

A: 629-41-4
1,8-Octanediol

B: 91898-32-7
8-(tert-butyldimethylsiloxy)octan-1-ol

Conditions

Conditions	Yield
With dimethylboron bromide; sodium hydrogencarbonate 1) CH2Cl2, -78 deg C, 1h, 2) THF, 5 min; Yield given. Multistep reaction;	A n/a B 81%
With dimethylboron bromide; sodium hydrogencarbonate 1) CH2Cl2, -78 deg C, 1h, 2) THF, 5 min; Yield given. Multistep reaction;	A 10% B n/a

: 114058-33-2
C30H50O3Si2

A: 629-41-4
1,8-Octanediol

B: 91898-32-7
8-(tert-butyldimethylsiloxy)octan-1-ol

Conditions

Conditions	Yield
With tetrabutyl ammonium fluoride In tetrahydrofuran; dichloromethane for 8h; Ambient temperature;	A 4% B 80%
With tetrabutyl ammonium fluoride In tetrahydrofuran; dichloromethane for 8h; Product distribution; Ambient temperature; var. silyl ethers; other reagents; selectivity of protecting group removal;	A 4% B 80%

: 1403675-09-1
(1-(allyloxy)(8-(tert-butyl)dimethylsiloxy))octane

: 629-41-4
1,8-Octanediol

Conditions

Conditions	Yield
With Pd(OH)2/C In isopropyl alcohol for 1.5h; Reflux;	78%

: 931-88-4, 22770-27-0, 3958-30-3
1,2-cyclooctene

: 629-41-4
1,8-Octanediol

Conditions

Conditions	Yield
With potassium permanganate; Tulsion T-40 exchange resin In dichloromethane; tert-butyl alcohol at 20℃; for 4h; oxidative cleavage;	73%

: 3710-30-3
1,7-Octadiene

A: 629-41-4
1,8-Octanediol

B: 2736-67-6
(5RS)-octane-1,5-diol

Conditions

Conditions	Yield
With 9-borabicyclo[3.3.1]nonane dimer; dimethylsulfide borane complex Product distribution;	A 11% B 67%

: 153164-82-0
1-(allyloxy)-8-(prop-2-yn-1-yloxy)octane

A: 629-41-4
1,8-Octanediol

B: 153164-83-1
8-allyloxyoctan-1-ol

Conditions

Conditions	Yield
With Pd(OH)2/C In isopropyl alcohol for 2h; Reflux;	A 54% B 36%

: (1-((8-benzyloxy)octyloxy)methyl)-4-methoxybenzene

A: 629-41-4
1,8-Octanediol

B: 162843-88-1
8-((4-methoxybenzyl)oxy)octan-1-ol

Conditions

Conditions	Yield
With Pd(OH)2/C In isopropyl alcohol for 3h; Reflux;	A 47% B 49%

: 1403675-07-9
1,8-bis(4-methoxybenzyloxy)octane

A: 629-41-4
1,8-Octanediol

B: 162843-88-1
8-((4-methoxybenzyl)oxy)octan-1-ol

Conditions

Conditions	Yield
With Pd(OH)2/C In methanol for 5h; Reflux;	A 46% B 24%

: 86565-05-1
1,8-Bis(trifluorosilyl)octane

: 629-41-4
1,8-Octanediol

Conditions

Conditions	Yield
With 3-chloro-benzenecarboperoxoic acid In N,N-dimethyl-formamide for 3h; r.t. then 50 deg C;	35%

: 71-36-3
butan-1-ol

: 629-41-4
1,8-Octanediol

Conditions

Conditions	Yield
Multistep reaction;	33%

: lithium (4-oxidobutyl)lithium

: 629-41-4
1,8-Octanediol

Conditions

Conditions	Yield
With copper dichloride In tetrahydrofuran at -78℃; for 0.75h;	33%

: 505-48-6
octane-1,8-dioic acid

: 629-41-4
1,8-Octanediol

Conditions

Conditions	Yield
With potassium hydroxide; samarium diiodide In tetrahydrofuran; water for 0.01h; Ambient temperature;	23%
With cobalt(II) oxide; hydrogen In 1,4-dioxane at 189.84℃; under 30003 Torr; for 10h; Autoclave;	94.8 %Chromat.

: 50601-65-5
octa-2,4,6-triyne-1,8-diol

: 629-41-4
1,8-Octanediol

Conditions

Conditions	Yield
With ethyl acetate; platinum Hydrogenation;
With diethyl ether; nickel at 150℃; under 73550.8 Torr; Hydrogenation;

: 15808-23-8
3,5-octadiyn-1,8-diol

: 629-41-4
1,8-Octanediol

Conditions

Conditions	Yield
With platinum(IV) oxide; acetic acid ester Hydrogenation;

: 58471-75-3
2,6-octadiyne-1,8-diol

A: 629-41-4
1,8-Octanediol

B: 111-87-5
octanol

Conditions

Conditions	Yield
With ethanol; hydrogen; platinum

: 1732-09-8
dimethyl subarate

: 629-41-4
1,8-Octanediol

Conditions

Conditions	Yield
With lithium aluminium tetrahydride; diethyl ether
With ethanol; sodium
With ethanol; sodium
With ethanol; sodium

: 106-99-0
buta-1,3-diene

: 629-41-4
1,8-Octanediol

Conditions

Conditions	Yield
With Dimethyl ether; sodium; sodium chloride at -23℃; beim Einleiten von Sauerstoff in Gegenwart von p-Terphenyl und Isooctan und Hydrieren des Reaktionsprodukts an Palladium/Kohle in Aether;

: 3049-34-1
octa-2,4,6-trienedial

: 629-41-4
1,8-Octanediol

Conditions

Conditions	Yield
With hydrogen; nickel In methanol

: 672-22-0
5tF,6rF,13tF',14rF'-tetrahydroxy-docosanoic acid

: 629-41-4
1,8-Octanediol

Conditions

Conditions	Yield
(i) NaIO4, aq. H2SO4, EtOH, (ii) NaBH4, NaOH; Multistep reaction;

: 55110-76-4
(8Z)-heptadec-8-en-1-ol

: 629-41-4
1,8-Octanediol

Conditions

Conditions	Yield
(i) O3, AcOEt, (ii) LiAlH4, Py; Multistep reaction;

: 75-21-8
oxirane

: 110-52-1
1,4-dibromo-butane

: 629-41-4
1,8-Octanediol

Conditions

Conditions	Yield
With magnesium; iodine 1. THF, reflux, 1h; 2. THF, r.t., 1h; Yield given. Multistep reaction;

: 5698-29-3
oxonan-2-one

: 629-41-4
1,8-Octanediol

Conditions

Conditions	Yield
With lithium triethylborohydride In various solvent(s) for 0.416667h; Thermodynamic data; ΔH;

: 931-88-4, 931-87-3
(Z)-Cyclooctene

A: 286-62-4
Cyclooctene oxide

B: 629-41-4
1,8-Octanediol

C: 27607-33-6
(1R,2S)-Cyclooctane-1,2-diol

Conditions

Conditions	Yield
With lithium aluminium tetrahydride; oxygen 1.) 80 deg C; Yield given. Multistep reaction. Yields of byproduct given. Title compound not separated from byproducts;
With lithium aluminium tetrahydride; oxygen 1) 80 grad C,101.3 kPa; Yield given. Multistep reaction. Yields of byproduct given. Title compound not separated from byproducts;

...Expand

: 629-41-4
1,8-Octanediol

: 50816-19-8
8-bromooctanol

Conditions

Conditions	Yield
With hydrogen bromide In water; toluene for 8h; Reflux;	100%
With hydrogen bromide In water; toluene for 8h; Reflux;	100%
With hydrogen bromide In toluene Heating;	99%

aqueous sodium hypochlorite: aqueous sodium hypochlorite

: 629-41-4
1,8-Octanediol

: sodium phosphate

A: 638-54-0
1,8-octanedial

B: 105910-44-9
dodeca-1,11-diene-3,10-diol

Conditions

Conditions	Yield
With potassium bromide; cyfluthrin In dichloromethane; water	A 100% B n/a

...Expand

: 629-41-4
1,8-Octanediol

: 53742-62-4
anilino(tert-butyldimethyl)silane

: 1,8-bis(tert-butyldimethylsiloxy)octane

Conditions

Conditions	Yield
With tetrabutyl ammonium fluoride In N,N-dimethyl-formamide at 20℃; for 1h;	99%

: 629-41-4
1,8-Octanediol

: 2162-99-4
1,8-dichlorooctane

Conditions

Conditions	Yield
With Amberlite IRA 93 (PCl5 form) In hexane for 5h; Heating;	98%
With oxalyl dichloride; chloro(triphenyl)phosphonium chloride In chloroform-d1 at 20℃; for 7h; Appel reaction;	71%
With toluene-4-sulfonic acid; 1-butyl-3-methylimidazolium chloride In toluene at 200℃; under 10343 Torr; for 0.166667h; microwave irradiation;	50%
With pyridine; thionyl chloride
Multi-step reaction with 2 steps 1: cooling 2: 94 percent / hexabutylguanidinium chloride / 4 h / 120 °C View Scheme

: 110-87-2
3,4-dihydro-2H-pyran

: 629-41-4
1,8-Octanediol

: 51326-52-4
8-(tetrahydro-2H-pyran-2-yloxy)octan-1-ol

Conditions

Conditions	Yield
With Dowex 50X2 In toluene at 30℃; for 5h;	98%
With Dowex50WX2 In toluene at 30℃; for 5h;	98%
With Dowex 50x2 In toluene at 30℃; for 5h;	98%

: 629-41-4
1,8-Octanediol

: 18162-48-6
tert-butyldimethylsilyl chloride

: 91898-32-7
8-(tert-butyldimethylsiloxy)octan-1-ol

Conditions

Conditions	Yield
Stage #1: 1,8-Octanediol With 1H-imidazole In dichloromethane at 0℃; for 0.25h; Stage #2: tert-butyldimethylsilyl chloride In dichloromethane at 0 - 20℃; for 1h;	98%
With dmap; triethylamine In dichloromethane Ambient temperature;	72%
Stage #1: 1,8-Octanediol With sodium hydride In tetrahydrofuran at 20℃; for 2h; Stage #2: tert-butyldimethylsilyl chloride In tetrahydrofuran at 20℃;	67%

: 124-04-9
Adipic acid

: 629-41-4
1,8-Octanediol

: 97-67-6
(S)-Malic acid

poly(octanedioladipate-co-octanediolmaleate), Mw: 11200, Mw/Mn: 2.44; Monomer(s): 1,8-octanediol; adipic acid; L-malic acid: poly(octanedioladipate-co-octanediolmaleate), Mw: 11200, Mw/Mn: 2.44; Monomer(s): 1,8-octanediol; adipic acid; L-malic acid

Conditions

Conditions	Yield
With novozyme 435 at 70℃; under 15.0015 - 45.0045 Torr; for 48h; Enzymatic reaction;	98%

...Expand

: 629-41-4
1,8-Octanediol

: 1609-86-5
Tert-butyl isocyanate

: 1417339-51-5
1,8-bis(N-tert-butylcarbamoyloxy)octane

Conditions

Conditions	Yield
With MoCl2O2(dmf)2 In dichloromethane at 20℃; for 0.5h; Inert atmosphere;	98%

: 629-41-4
1,8-Octanediol

: 505-48-6
octane-1,8-dioic acid

Conditions

Conditions	Yield
With C24H33IrN4O3; water; sodium hydroxide for 18h; Reflux;	97%
With sodium bromate; sodium hydrogensulfite In acetonitrile for 2h; Heating;	91%
With Iron(III) nitrate nonahydrate; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; potassium chloride; oxygen In 1,2-dichloro-ethane at 25℃; for 48h;	86%
With Iron(III) nitrate nonahydrate; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; potassium chloride; oxygen In 1,2-dichloro-ethane at 20℃; for 48h; Schlenk technique;	86%

: 629-41-4
1,8-Octanediol

: 100-39-0
benzyl bromide

: 1,8-bis(benzyloxy)octane

Conditions

Conditions	Yield
Stage #1: 1,8-Octanediol With sodium hydride In N,N-dimethyl-formamide at 0℃; for 0.25h; Stage #2: benzyl bromide In N,N-dimethyl-formamide at 0 - 20℃; for 3h;	97%
Stage #1: 1,8-Octanediol With sodium hydride In tetrahydrofuran at 60℃; for 0.5h; Substitution; Stage #2: benzyl bromide In tetrahydrofuran at 60℃; for 12h; Substitution;

: 124-04-9
Adipic acid

: 629-41-4
1,8-Octanediol

: 97-67-6
(S)-Malic acid

poly(octanedioladipate-co-octanediolmaleate), Mw: 17800, Mw/Mn: 3.42; Monomer(s): 1,8-octanediol; adipic acid; L-malic acid: poly(octanedioladipate-co-octanediolmaleate), Mw: 17800, Mw/Mn: 3.42; Monomer(s): 1,8-octanediol; adipic acid; L-malic acid

Conditions

Conditions	Yield
With novozyme 435 In hexane at 70℃; for 48h; Enzymatic reaction;	97%

...Expand

: 629-41-4
1,8-Octanediol

: 2130-96-3
O-benzyl-N-tert-butoxycarbonyl-L-tyrosine

: bis-N-Boc-O-benzl-L-tyrosine-octane-1,8-diester

Conditions

Conditions	Yield
With 4-(dimethylamino)pyridinium tosylate; diisopropyl-carbodiimide In dichloromethane at 0℃; Inert atmosphere;	97%

: 629-41-4
1,8-Octanediol

: 22054-14-4
8-hydroxyoctanal

Conditions

Conditions	Yield
With copper(l) iodide; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; N,N,N,N,-tetramethylethylenediamine; oxygen In acetonitrile at 20℃; for 30h;	97%

: 629-41-4
1,8-Octanediol

: 109216-50-4
(1S,5R,7S)-1,5,7-Trimethyl-2,4-dioxo-3-aza-bicyclo[3.3.1]nonane-7-carbonyl chloride

: 129786-98-7
C32H48N2O8

Conditions

Conditions	Yield
With dmap; triethylamine In dichloromethane Heating;	96%

: 629-41-4
1,8-Octanediol

: 98-59-9
p-toluenesulfonyl chloride

: 36247-32-2
1,8-bis(p-toluenesulfonyloxy)octane

Conditions

Conditions	Yield
With pyridine at 0℃; for 3h;	96%
With pyridine at 0℃; for 2.5h;	91%
With pyridine In dichloromethane at 5 - 15℃; for 0.333333h;	90.9%

: 629-41-4
1,8-Octanediol

: 76-83-5
trityl chloride

: 38257-96-4
8-[(triphenylmethyl)oxy]octanol

Conditions

Conditions	Yield
With dmap; triethylamine In dichloromethane at 20℃; for 24h;	96%
With triethylamine In dichloromethane at 20℃; for 24h; Inert atmosphere;	60%
In pyridine; dichloromethane Ambient temperature;	55%
With pyridine In N,N-dimethyl-formamide at 20℃; for 1h;
With dmap; triethylamine In dichloromethane at 20℃; for 24h;

: 629-41-4
1,8-Octanediol

: 754-05-2
ethenyltrimethylsilane

: 16654-42-5
1,8-bis(trimethylsiloxy)octane

Conditions

Conditions	Yield
Wilkinson's catalyst In toluene at 130℃; for 3h;	96%

: 124-04-9
Adipic acid

: 629-41-4
1,8-Octanediol

: 97-67-6
(S)-Malic acid

poly(octanedioladipate-co-octanediolmaleate), Mw: 12400, Mw/Mn: 2.15; Monomer(s): 1,8-octanediol; adipic acid; L-malic acid: poly(octanedioladipate-co-octanediolmaleate), Mw: 12400, Mw/Mn: 2.15; Monomer(s): 1,8-octanediol; adipic acid; L-malic acid

Conditions

Conditions	Yield
With novozyme 435 In toluene at 70℃; for 48h; Enzymatic reaction;	96%

...Expand

: 124-04-9
Adipic acid

: 629-41-4
1,8-Octanediol

: 97-67-6
(S)-Malic acid

poly(octanedioladipate-co-octanediolmaleate), Mw: 14500, Mw/Mn: 3.14; Monomer(s): 1,8-octanediol; adipic acid; L-malic acid: poly(octanedioladipate-co-octanediolmaleate), Mw: 14500, Mw/Mn: 3.14; Monomer(s): 1,8-octanediol; adipic acid; L-malic acid

Conditions

Conditions	Yield
With novozyme 435 In 2,2,4-trimethylpentane at 70℃; for 48h; Enzymatic reaction;	96%

...Expand

: 110-87-2
3,4-dihydro-2H-pyran

: 629-41-4
1,8-Octanediol

A: 51326-52-4
8-(tetrahydro-2H-pyran-2-yloxy)octan-1-ol

B: 69891-87-8
1,8-di(2-terahydropyranyloxy)-octane

Conditions

Conditions	Yield
With Dowex 50W x 2 (50-100 mesh) In toluene at 30℃; for 4.5h;	A 95% B 2%
With aluminium trichloride; silica gel In 1,2-dichloro-ethane at 20℃; for 1.9h;	A 92% B 3%
copper(II) sulfate In acetonitrile at 20℃; for 12h;	A 83% B n/a

...Expand

: 629-41-4
1,8-Octanediol

: 124-63-0
methanesulfonyl chloride

: 15886-83-6
octane-1,14-diol dimesylate

Conditions

Conditions	Yield
With triethylamine In dichloromethane at 0 - 20℃;	95%
With pyridine at 0℃;	69%

: 629-41-4
1,8-Octanediol

: 3768-55-6
N-trimethylsilylaniline

: 16654-42-5
1,8-bis(trimethylsiloxy)octane

Conditions

Conditions	Yield
With tetrabutyl ammonium fluoride In N,N-dimethyl-formamide at 20℃; for 0.0833333h;	95%

: 124-04-9
Adipic acid

: 629-41-4
1,8-Octanediol

polymer, Mw 26100 Da by SEC, PDI 2.8 by SEC; monomer(s): adipic acid; 1,8-octanediol: polymer, Mw 26100 Da by SEC, PDI 2.8 by SEC; monomer(s): adipic acid; 1,8-octanediol

Conditions

Conditions	Yield
With novozyme 435 at 80℃; for 42h;	95%

: 629-41-4
1,8-Octanediol

: 408322-03-2
2,2,5-trimethyl-1,3-dioxane-5-carboxylic anhydride

: 1431636-36-0
1,8-bis-((2,2,5-trimethyl-1,3-dioxan-5-yl)propanoyloxy)octane

Conditions

Conditions	Yield
With dmap In pyridine; dichloromethane at 20℃; for 4h; Inert atmosphere;	95%

: 629-41-4
1,8-Octanediol

: 629-40-3
octanedinitrile

Conditions

Conditions	Yield
With ammonium hydroxide; 1,3-Diiodo-5,5-dimethyl-2,4-imidazolidinedione at 60℃; for 24h;	94%
With ammonium hydroxide; 1,3-Diiodo-5,5-dimethyl-2,4-imidazolidinedione at 60℃; for 24h;	94%

: 124-04-9
Adipic acid

: 629-41-4
1,8-Octanediol

: 97-67-6
(S)-Malic acid

poly(octanedioladipate-co-octanediolmaleate), Mw: 5400, Mw/Mn: 1.95; Monomer(s): 1,8-octanediol; adipic acid; L-malic acid: poly(octanedioladipate-co-octanediolmaleate), Mw: 5400, Mw/Mn: 1.95; Monomer(s): 1,8-octanediol; adipic acid; L-malic acid

Conditions

Conditions	Yield
With novozyme 435 In tetrahydrofuran at 55℃; for 48h; Enzymatic reaction;	94%

...Expand

: 629-41-4
1,8-Octanediol

: 64-19-7
acetic acid

: 40646-17-1
8-hydroxyoctan-1-ol acetate

Conditions

Conditions	Yield
With HY-Zeolite In chloroform for 3.5h; Heating;	93%
With sulfuric acid In toluene at 75℃; for 15h;	89%
With sulfuric acid In water; pentane for 12h; Reflux;	68%

: 110-87-2
3,4-dihydro-2H-pyran

: 629-41-4
1,8-Octanediol

: 69891-87-8
1,8-di(2-terahydropyranyloxy)-octane

Conditions

Conditions	Yield
copper(II) sulfate In acetonitrile at 20℃; for 12h;	93%

1,8-Octanediol Chemical Properties

IUPAC Name: Octane-1,8-diol
Synonyms of 1,8-Octanediol (CAS NO.629-41-4): EINECS 211-090-8 ; Octane-1,8-diol
CAS NO: 629-41-4
Molecular Formula of 1,8-Octanediol (CAS NO.629-41-4): C₈H₁₈O₂
Molecular Weight: 146.2273
Molecular Structure:

Product Categories: Industrial/Fine Chemicals ; Miscellaneous ; alpha,omega-Alkanediols ; alpha,omega-Bifunctional Alkanes ; Monofunctional & alpha,omega-Bifunctional Alkanes ; Linear hydrocarbon series
Melting Point: 57-61 °C
Polar Surface Area: 18.46 Å²
Index of Refraction: 1.454
Molar Refractivity: 42.18 cm³
Molar Volume: 155.6 cm³
Surface Tension: 37 dyne/cm
Density of 1,8-Octanediol (CAS NO.629-41-4): 0.939 g/cm³
Flash Point: 128 °C
Enthalpy of Vaporization: 60.07 kJ/mol
Boiling Point: 278.8 °C at 760 mmHg
Vapour Pressure: 0.000507 mmHg at 25°C

1,8-Octanediol Uses

It can be used as intermediates of cosmetics, plasticizers and specialty additives.

1,8-Octanediol Production

It is derived by OCTYLDODECYL ETHYLHEXANOATE as raw materials, copper - chromium oxide as catalyst and hydrogenation at high temperature under high pressure.

1,8-Octanediol Safety Profile

Hazard Codes: Irritant Xi,Xn
Risk Statements: 20/21/22-36/37/38
R20/21/22: Harmful by inhalation, in contact with skin and if swallowed.
R36/37/38: Irritating to eyes, respiratory system and skin.
Safety Statements: 26-37/39
S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S37/39: Wear suitable gloves and eye/face protection.
WGK Germany: 3
HS Code: 29053980

Product Name

Octane-1,8-diol

Synthetic route

1,8-Octanediol Chemical Properties

1,8-Octanediol Uses

1,8-Octanediol Production

1,8-Octanediol Safety Profile

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