Chemical Properties of Xylotriose, permethyl

Xylotriose, permethyl

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InChI
InChI=1S/C23H42O13/c1-24-12-9-33-22(19(29-6)15(12)25-2)36-14-11-34-23(20(30-7)17(14)27-4)35-13-10-32-21(31-8)18(28-5)16(13)26-3/h12-23H,9-11H2,1-8H3/t12-,13-,14-,15+,16+,17+,18-,19-,20-,21-,22+,23+/m0/s1
InChI Key
IVVVORJOYSYZNI-HGKZIHKDSA-N
Formula
C23H42O13
SMILES
COC1COC(OC2COC(OC3COC(OC)C(OC)C3OC)C(OC)C2OC)C(OC)C1OC
Molecular Weight1
526.57
Sources

Physical Properties

Property Value Unit Source
Δf -1161.62 kJ/mol Joback Calculated Property
Δfgas -2256.35 kJ/mol Joback Calculated Property
Δfus 76.29 kJ/mol Joback Calculated Property
Δvap 102.93 kJ/mol Joback Calculated Property
logPoct/wat -0.42 Crippen Calculated Property
Pc 915.50 kPa Joback Calculated Property
Tboil 1047.31 K Joback Calculated Property
Tc 1282.23 K Joback Calculated Property
Tfus 634.96 K Joback Calculated Property
Vc 1.36 m3/kg-mol Joback Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas 1481.53 J/mol×K 1047.31 Joback Calculated Property
η 0.00 Pa×s 1047.31 Joback Calculated Property

Molecular Descriptors

Joback and Reid Groups
-O- (nonring) 10
-O- (ring) 3
-CH3 8
>CH- (ring) 12
-CH2- (ring) 3

Similar Compounds

Xylobiose, permethyl. Xylotetraose, permethyl. Maltotetraose, permethyl. Maltotriose, permethyl. «beta»-D-Mannopyranoside, 1-(2-butyl), permethylated, # 2. «alpha»-D-Mannopyranoside, 1-(2-butyl), permethylated, # 1. «alpha»-D-Galactopyranoside, 1-(2-butyl), permethylated, # 2. «beta»-D-Glucopyranoside, 1-(2-butyl), permethylated, # 2. «beta»-D-Mannopyranoside, 1-(2-butyl), permethylated, # 1. «alpha»-D-Mannopyranoside, 1-(2-butyl), permethylated, # 2. «alpha»-D-Galactopyranoside, 1-(2-butyl), permethylated, # 1. «alpha»-D-Glucopyranoside, 1-(2-butyl), permethylated, # 1. «beta»-D-Galactopyranoside, 1-(2-butyl), permethylated, # 2. «beta»-D-Galactopyranoside, 1-(2-butyl), permethylated, # 1. «alpha»-D-Glucopyranoside, 1-(2-butyl), permethylated, # 2.

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