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1,4-Nonanediol is an organic compound with the chemical formula C9H20O2. It is a diol, meaning it contains two hydroxyl (-OH) groups, and is part of the alkane family with a nine-carbon chain. The hydroxyl groups are located at the first and fourth carbon atoms, hence the name 1,4-Nonanediol. This colorless liquid is soluble in water and has a sweet, floral odor. It is used in the synthesis of various chemicals, including fragrances, pharmaceuticals, and plasticizers. Due to its potential health risks, it is important to handle 1,4-Nonanediol with care, as it can cause irritation to the eyes, skin, and respiratory system.

2430-73-1

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2430-73-1 Usage

Physical state

Colorless, viscous liquid

Uses

a. Production of pharmaceuticals
b. Production of cosmetics
c. Production of plasticizers

Primary utilization

Synthetic intermediate in the manufacturing of fragrances, lubricants, and surfactants

Additional uses

a. Solvent
b. Curing agent for epoxy resins

Toxicity

Low toxicity

Safety

Generally regarded as a safe ingredient in consumer products

Handling

Should be handled with caution and in accordance with proper safety measures

Check Digit Verification of cas no

The CAS Registry Mumber 2430-73-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,3 and 0 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2430-73:
(6*2)+(5*4)+(4*3)+(3*0)+(2*7)+(1*3)=61
61 % 10 = 1
So 2430-73-1 is a valid CAS Registry Number.

2430-73-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4-dihydroxynonane

1.2 Other means of identification

Product number -
Other names 1,4-nonanediol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:2430-73-1 SDS

2430-73-1Relevant academic research and scientific papers

Oxygen-directed intramolecular hydroboration

Rarig, Robert-Andre F.,Scheideman, Matthew,Vedejs, Edwin

supporting information; body text, p. 9182 - 9183 (2009/02/03)

Metal-free homoallylic oxygen-directed intramolecular hydroboration is reported. Regioselectivities from 20:1 to 82:1 favoring the 1,3-dioxy-substituted products have been achieved using Me2S·BH3/TfOH followed by standard oxidative workup. Branching at the C5 position improves regioselectivity. Copyright

Synthesis and Occurrence of Oxoaldehydes in Used Frying Oils

Takeoka, Gary R.,Buttery, Ron G.,Perrino, Charles T.

, p. 22 - 26 (2007/10/02)

As part of our efforts to identify volatile decomposition products in used frying oils, a series of 4- and 5-oxoaldehydes were synthesized, purified, and characterized by gas chromatography, gas chromatography-mass spectrometry, gas-chromatography-Fourier transform infrared spectrometry, and nuclear magnetic resonance spectrometry.Oxoaldehydes have been proposed as possible precursors of alkylfurans, which have potential anticancer effects.In a model reaction 4-oxononanal was refluxed in hexane for 40 days and only trace amounts of 2-pentylfuran were produced, suggesting that it is not a major precursor of the furan.The volatile constituents of used frying oils obtained from commercial food processors were studied, and 4-oxohexanal, 4-oxooctanal, 4-oxononanal, and 4-oxodecanal were identified.Keywords: Oxoaldehydes; odor threshold; frying oil

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