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Key Documents

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N29600

Sigma-Aldrich

1,9-Nonanediol

98%

Sinónimos:

Nonamethylene glycol

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About This Item

Fórmula lineal:
HO(CH2)9OH
Número de CAS:
3937-56-2
Peso molecular:
160.25
Beilstein/REAXYS Number:
1737531
EC Number:
223-517-5
MDL number:
MFCD00002991
UNSPSC Code:
12352100
PubChem Substance ID:
24897607
NACRES:
NA.22

assay

98%

form

crystals

bp

177 °C/15 mmHg (lit.)

mp

45-47 °C (lit.)

SMILES string

OCCCCCCCCCO

InChI

1S/C9H20O2/c10-8-6-4-2-1-3-5-7-9-11/h10-11H,1-9H2

InChI key

ALVZNPYWJMLXKV-UHFFFAOYSA-N

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hcodes

H412

Hazard Classifications

Aquatic Chronic 3

Storage Class

11 - Combustible Solids

wgk_germany

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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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
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
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
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
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

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