N29600
1,9-Nonanediol
98%
Synonym(s):
Nonamethylene glycol
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About This Item
Linear Formula:
HO(CH2)9OH
CAS Number:
Molecular Weight:
160.25
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
223-517-5
Beilstein/REAXYS Number:
1737531
MDL number:
Product Name
1,9-Nonanediol, 98%
InChI
1S/C9H20O2/c10-8-6-4-2-1-3-5-7-9-11/h10-11H,1-9H2
InChI key
ALVZNPYWJMLXKV-UHFFFAOYSA-N
SMILES string
OCCCCCCCCCO
assay
98%
form
crystals
bp
177 °C/15 mmHg (lit.)
mp
45-47 °C (lit.)
Quality Level
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Related Categories
hcodes
pcodes
Hazard Classifications
Aquatic Chronic 3
Storage Class
11 - Combustible Solids
wgk
WGK 2
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
Eyeshields, Gloves, type N95 (US)
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Lucila Navarro et al.
Journal of pharmaceutical sciences, 106(8), 2106-2114 (2017-05-26)
Paclitaxel (PTX) incorporation in poly(lactic-co-glycolic acid) (PLGA) matrices produce films with high tensile rigidity and slow release that fail to deliver the required release rate for most biomedical applications such as in drug eluting stents and cancer treatments. To modify
Leila Hojabri et al.
Biomacromolecules, 11(4), 911-918 (2010-03-18)
An unsaturated terminal diol, 1,18-octadec-9-endiol (ODEDO), and a saturated terminal diol, 1,9-nonanediol (NDO), were synthesized from oleic acid. The feasibility of utilizing these new diols for the production of thermoplastic polyurethanes (TPUs) was demonstrated by reacting them with a fatty
Yuta Toyama et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 197, 148-152 (2018-01-10)
Even-odd alternation of the melting points of α,ω-disubstituted linear alkanes such as alkane-α,ω-diols, alkane-α,ω-dinitriles and α,ω-diaminoalkanes is well known. Melting points for compounds with an even number of carbons in their alkyl chains are systematically higher than those for compounds
M Y Ma et al.
Biochemistry, 32(7), 1751-1758 (1993-02-23)
Double-stranded oligodeoxyribonucleotides or single-stranded oligoribonucleotides with specific secondary structure have been proposed as potential antagonists to target nucleic acid-binding proteins (the sense approach). A major limitation of this strategy is that these derivatives are generally considered to be too large
Kashif Ahmad Ghaffar et al.
Pharmaceutics, 12(2) (2020-02-27)
Triterpenes from the outer bark of birch have many beneficial biological and pharmacological activities. In particular, its wound healing efficacy is of paramount importance. Apart from that, particles of a birch bark dry extract aggregate into a three dimensional network
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