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N29600

Sigma-Aldrich

1,9-Nonanediol

98%

Synonym(s):

Nonamethylene glycol

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About This Item

Linear Formula:
HO(CH2)9OH
CAS Number:
3937-56-2
Molecular Weight:
160.25
Beilstein:
1737531
EC Number:
223-517-5
MDL number:
MFCD00002991
UNSPSC Code:
12352100
PubChem Substance ID:
24897607
NACRES:
NA.22

Quality Level

100

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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Hazard Statements

H412

Precautionary Statements

P273 - P501

Hazard Classifications

Aquatic Chronic 3

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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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
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
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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