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Nonanoic acid

CAS No.
112-05-0
Chemical Name:
Nonanoic acid
Synonyms
NONANE;PELARGONIC ACID;nonanoic;pelargonic;N-NONANOIC ACID;NONOIC ACID;Pelargic acid;pelargonate (9:0);n-Nonanoic acid,97%;Nonanoic acid (Pelargonic)
CBNumber:
CB9203118
Molecular Formula:
C9H18O2
Molecular Weight:
158.24
MDL Number:
MFCD00004433
MOL File:
112-05-0.mol
MSDS File:
SDS
Last updated:2024-11-15 19:19:13

Nonanoic acid Properties

Melting point 9 °C (lit.)
Boiling point 268-269 °C (lit.)
Density 0.906 g/mL at 25 °C (lit.)
vapor density 5.5 (vs air)
vapor pressure <0.1 mm Hg ( 20 °C)
refractive index n20/D 1.432(lit.)
FEMA 2784 | NONANOIC ACID
Flash point 212 °F
storage temp. 2-8°C
solubility 0.3g/l
form Liquid
pka 4.96(at 25℃)
color Clear colorless
PH 4(1 mM solution);3.49(10 mM solution);2.98(100 mM solution);
Odor at 10.00 % in dipropylene glycol. waxy dirty cheese cultured dairy
Odor Type waxy
explosive limit 0.8-9%(V)
Water Solubility NEGLIGIBLE
Merck 14,7070
JECFA Number 102
BRN 1752351
Dielectric constant 13.9(25℃)
LogP 3.4 at 25℃
Substances Added to Food (formerly EAFUS) NONANOIC ACID
FDA 21 CFR 172.515
CAS DataBase Reference 112-05-0(CAS DataBase Reference)
EWG's Food Scores 1
FDA UNII 97SEH7577T
NIST Chemistry Reference Nonanoic acid(112-05-0)
EPA Substance Registry System Nonanoic acid (112-05-0)
Pesticides Freedom of Information Act (FOIA) Pelargonic acid

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H315-H319-H412
Precautionary statements  P264-P273-P280-P302+P352-P305+P351+P338-P332+P313
Hazard Codes  C
Risk Statements  34
Safety Statements  26-28-36/37/39-45-28A
RIDADR  UN 3265 8/PG 3
WGK Germany  1
RTECS  RA6650000
Autoignition Temperature 405 °C
TSCA  Yes
HazardClass  8
PackingGroup  III
HS Code  29159080
Toxicity LD50 i.v. in mice: 224±4.6 mg/kg (Or, Wretlind)
NFPA 704
0
2 0

Nonanoic acid price More Price(38)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich W278430 Nonanoic Acid natural, 98%, FG 112-05-0 500g $270 2024-03-01 Buy
Sigma-Aldrich W278430 Nonanoic Acid natural, 98%, FG 112-05-0 1kg $380 2024-03-01 Buy
Sigma-Aldrich W278430 Nonanoic Acid natural, 98%, FG 112-05-0 5kg $1900 2024-03-01 Buy
Sigma-Aldrich W278408 Nonanoic Acid ≥96%, FG 112-05-0 1kg $89.6 2024-03-01 Buy
Sigma-Aldrich W278408 Nonanoic Acid ≥96%, FG 112-05-0 5kg $193 2024-03-01 Buy
Product number Packaging Price Buy
W278430 500g $270 Buy
W278430 1kg $380 Buy
W278430 5kg $1900 Buy
W278408 1kg $89.6 Buy
W278408 5kg $193 Buy

Nonanoic acid Chemical Properties,Uses,Production

Description

Nonanoic acid (also known as pelargonic acid; chemical formula: CH3 (CH2)7COOH) is a kind of organic carboxylic acid compound. It is naturally existed in the oil of pelargonium in the form of esters. It is commonly used in conjunction with glyphosate which is a kind of non-selective herbicide in order to obtain a quick burn-down effect in the control of weeds in turfgrass. It is also a potent antifungal agent which can inhibit spore germination and mycelial growth of pathogenic fungi. Its synthetic esters, such as methyl nonanoate can be used as flavorings. Moreover, it can also be used in the preparation of plasticizers and lacquers. It can also be potentially used for the treatment of seizures.

References

https://en.wikipedia.org/wiki/Nonanoic_acid
http://www.abcam.com/nonanoic-acid-pelargonic-acid-ab143891.html

Description

Nonanoic acid , also called pelargonic acid, is an organic compound composed of a nine - carbon chain terminating in a carboxylic acid with structural formula CH3(CH2)7COOH. Nonanoic acid forms esters—nonanoates. It is a clear, oily liquid with an unpleasant, rancid odor. It is nearly insoluble in water, but very soluble in chloroform, ether, and hexane.
Its refractive index is 1.4322. Its critical point is at 712 K ( 439 °C ) and 2.35 MPa.

Chemical Properties

Colorless or yellowish, combustible, oily liquid. Faint odor.

Chemical Properties

clear colorless liquid

Chemical Properties

Nonanoic acid has a fatty, characteristic odor and a corresponding unpleasant taste. This compound is also reported as having a cheese, waxy flavor

Chemical Properties

Nonanoic acid has a fatty, characteristic odor and a corresponding unpleasant taste. May be prepared by oxidation of methylnonyl ketone; by oxidation of oleic acid; or from heptyl iodide via malonic ester synthesis.

Originator

Pellar,Crookes Barnes, US ,1960

Occurrence

Nonanoic acid is a fatty acid which occurs naturally as esters in the oil of pelargonium. Synthetic esters, such as methyl nonanoate, are used as flavorings.
Nonanoic acid is also used in the preparation of plasticizers and lacquers.
The derivative 4-nonanoylmorpholine is an ingredient in some pepper sprays.
The ammonium salt of nonanoic acid, ammonium nonanoate, is used as an herbicide.

Uses

The primary uses of this acid are in organic synthesis and in the manufacture of lacquers, plastics, pharmaceuticals, synthetic odors and flavorings, gasoline additives, flotation agents, lubricants, and vinyl plasticizers. Nonanoic acid has found some use in pharmaceutical preparations and as a topical bactericide and fungicide. It is also used in herbicides.

Uses

In the production of hydrotropic salts (hydrotropic salts form aqueous solutions which dissolve sparingly soluble substances to a greater extent than water); in the manufacture of lacquers, plastics.

Uses

Intermediates of Liquid Crystals

Definition

ChEBI: A C9 straight-chain saturated fatty acid which occurs naturally as esters of the oil of pelargonium. Has antifungal properties, and is also used as a herbicide as well as in the preparation of plasticisers and lacquers.

Preparation

Nonanoic acid is produced by malonic ester synthesis, from Heptyl iodide.

Manufacturing Process

A body of liquid, 18 inches high, comprising a 35% (by weight) solution of technical (95%) oleic acid in n-propanol, is maintained at a temperature of 86°C in a reactor. The solution also contains dissolved therein 0.042% by weight of cobalt, in the form of cobalt naphthenate. From the bottom of the reactor very fine bubbles of air are passed into and through the solution at the rate of about 0.3 cubic feet per minute, measured at standard conditions, per square foot for 72 hours. The gases leaving the reactor are first passed through an ice water reflux condenser and then vented to the atmosphere. At the end of the 72 hour period the reaction mixture is separated into its components. It is found that 60% of the oleic acid has been consumed in the reaction. For each pound of oleic acid consumed there are obtained 0.30 pound of azelaic acid (representing an efficiency of 46%, calculated on the basis that the technical oleic acid is 100% oleic acid), 0.13 pound of pelargonic acid (representing an efficiency of 23%) and 0.21 pound of 9,10dihydroxystearic acid (representing an efficiency of 19%).

Therapeutic Function

Fungicide

Aroma threshold values

Detection: 3 to 9 ppm

Taste threshold values

Taste characteristics at 10 ppm: fatty, waxy, and cheesy with a mild, sweet, creamy background

Synthesis Reference(s)

Journal of the American Chemical Society, 93, p. 195, 1971 DOI: 10.1021/ja00730a033
Organic Syntheses, Coll. Vol. 2, p. 474, 1943
Tetrahedron Letters, 9, p. 5689, 1968

General Description

Nonanoic acid occurs naturally in Pelargonium L′Her. It one of the flavor constituents of cooked rice, acerola fruit, licorice and yogurt.

Agricultural Uses

Herbicide, Fungicide: Pelargonic acid occurs naturally in many plants and animals. It is used to control the growth of weeds and as a blossom thinner for apple and pear trees. It is also used as a food additive; as an ingredient in solutions used to commercially peel fruits and vegetables

Trade name

CIRRASOL®-185A; ECONOSAN®; EMERY® 202 (mixture with n-octoic acid); EMFAC®-1202; HEXACID® C-9; PELARGON®; SCYTHE®; WEST AGRO ACID SANITIZER®

Safety Profile

Poison by intravenous route. Moderately toxic by ingestion. A severe skin and eye irritant. When heated to decomposition it emits acrid smoke and irritating fumes.

Synthesis

By oxidation of methylnonyl ketone; by oxidation of oleic acid; or from heptyl iodide via malonic ester synthesis

Potential Exposure

Pelargonic acid, a naturally occurring fatty acid herbicide/fungicide. It is used to control the growth of weeds and as a blossom thinner for apple and pear trees. It is also used as a food additive; as an ingredient in solutions used to commercially peel fruits and vegetables; in the manufacture of lacquers, plastics and pharmaceuticals.

Purification Methods

Esterify the acid with ethylene glycol and distil the ester. (This removes dibasic acids as undistillable residues.) The acid is regenerated by hydrolysing the ester in the usual way and is distilled in vacuo. [Beilstein 2 IV 1018.]

Incompatibilities

Heated vapors may form explosive mixture with air. May react violently with strong oxidizers, bromine, 90% hydrogen peroxide, phosphorus trichloride, silver powders or dust. Incompatible with strong bases and silver compounds; mixture with some silver compounds may form explosive salts of silver oxalate.

Waste Disposal

Do not discharge into drains or sewers. Dispose of waste material as hazardous waste using a licensed disposal contractor to an approved landfill. Contact a licensed disposal facility about surplus and non-recyclable solutions. Burn in a chemical incinerator equipped with an afterburner and scrubber. Extra care must be exercised as the material in an organic solvent is highly flammable. Consult with environmental regulatory agencies for guidance on acceptable disposal practices. Incineration with effluent gas scrubbing is recommended. Containers must be disposed of properly by following package label directions or by contacting your local or federal environmental control agency, or by contacting your regional EPA office.

64-18-6
111-66-0
112-05-0
Synthesis of Nonanoic acid from Formic acid and 1-OCTENE
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View Lastest Price from Nonanoic acid manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Nonanoic acid pictures 2024-11-15 Nonanoic acid
112-05-0
US $39.00 / mL 99.1% 10g TargetMol Chemicals Inc.
Nonanoic Acid/Pelargonic Acid pictures 2024-11-15 Nonanoic Acid/Pelargonic Acid
112-05-0
US $180.00 / kg 1kg 99% 20ton Hebei Zhuanglai Chemical Trading Co.,Ltd
Nonanoic acid pictures 2024-11-15 Nonanoic acid
112-05-0
US $60.00 / kg 1kg 99 5000 Hebei Zhuanglai Chemical Trading Co.,Ltd
  • Nonanoic acid pictures
  • Nonanoic acid
    112-05-0
  • US $39.00 / mL
  • 99.1%
  • TargetMol Chemicals Inc.
  • Nonanoic acid pictures
  • Nonanoic acid
    112-05-0
  • US $60.00 / kg
  • 99
  • Hebei Zhuanglai Chemical Trading Co.,Ltd
n-Nonanoic acid,90%,tech. Acid C9, Pelargonic acid nonanoic acid >=99.0% Nonanoic acid,Acid C9, Pelargonic acid n-Nonanoic acid, 97% 100GR n-Nonanoic acid, 97% 1KG Nonanoic-d4 Acid NONANOIC ACID FOR SYNTHESIS 1 L NONANOIC ACID FOR SYNTHESIS 100 ML Nonoic aci cirrasol185a Emery 1202 Emery's L-114 Emfac 1202 emfac1202 Hexacid C-9 hexacidc-9 n-Nonoic acid n-nonoicacid nonanoicacid(non-specificname) Nonansαure Nonylsαure n-Pelargonicacid pelargicacid Pelargon pelargon(russian) Pelargonsαure Pergonicacid PELARGONIC ACID (NONANOIC ACID) NONANOIC ACID 96+% NONANOIC ACID GRADE I NONANOIC ACID GRADE II Nonanoic acid 96% Grantrico n-Nonanoic acid Pelargonicacid,98% AKOS 222-43 SCYTHE RARECHEM AL BO 0187 OCTANE-1-CARBOXYLIC ACID N-NONYLIC ACID NONANOIC ACID NONYLIC ACID 1-nonanoic acid 1-Octanecarboxylic acid 1-octanecarboxylicacid acidenonyliquenormal acidepelargonique Cirrasol 185a n-Nonanoic acid, pract. n-Nonanoic acid, tech., 90% C9:0 FATTY ACID C9 ACID CARBOXYLIC ACID C9 GRANTRICO FEMA 2784 Nonanoic?Acid?(Pelargonic?Acid) acid c-9 AMMONIUMNONANOATE