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Sebacic acid

CAS No.
111-20-6
Chemical Name:
Sebacic acid
Synonyms
DECANEDIOIC ACID;sebacic;USAF hc-1;acidesebacique;SEBACIC ACID pure;n-Decanedioic acid;1,10-Decanedioic acid;Decanedicarboxylic acid;sebacate (decanedioate);1,8-OCTANEDICARBOXYLIC ACID
CBNumber:
CB0329394
Molecular Formula:
C10H18O4
Molecular Weight:
202.25
MDL Number:
MFCD00004440
MOL File:
111-20-6.mol
MSDS File:
SDS
Last updated:2024-11-05 19:05:58

Sebacic acid Properties

Melting point 133-137 °C (lit.)
Boiling point 294.5 °C/100 mmHg (lit.)
Density 1.21
vapor pressure 1 mm Hg ( 183 °C)
refractive index 1.422
Flash point 220 °C
storage temp. Store below +30°C.
solubility ethanol: 100 mg/mL
form Powder or Granules
pka 4.59, 5.59(at 25℃)
color White to off-white
Odor monoclinic prismatic tablets, wh. powd., fatty acid odor
Water Solubility 1 g/L (20 ºC)
Merck 14,8415
BRN 1210591
Stability Stable. Combustible. Incompatible with strong oxidizing agents, bases, reducing agents.
InChIKey CXMXRPHRNRROMY-UHFFFAOYSA-N
LogP 1.5 at 23℃
Indirect Additives used in Food Contact Substances SEBACIC ACID
FDA 21 CFR 175.105; 175.300; 175.320
CAS DataBase Reference 111-20-6(CAS DataBase Reference)
EWG's Food Scores 1
FDA UNII 97AN39ICTC
NIST Chemistry Reference Decanedioic acid(111-20-6)
EPA Substance Registry System Sebacic acid (111-20-6)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313-P261-P280a-P304+P340-P305+P351+P338-P405-P501a
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-36-24/25
WGK Germany  1
RTECS  VS0875000
TSCA  Yes
HS Code  29171310
Toxicity LD50 orally in Rabbit: 3400 - 14500 mg/kg LD50 dermal Rat > 2000 mg/kg
NFPA 704
0
1 0

Sebacic acid price More Price(52)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 8.00753 Sebacic acid for synthesis 111-20-6 100g $32.6 2024-03-01 Buy
Sigma-Aldrich 8.00753 Sebacic acid for synthesis 111-20-6 500g $91.4 2024-03-01 Buy
Sigma-Aldrich 8.00753 Sebacic acid for synthesis 111-20-6 1kg $147 2024-03-01 Buy
Sigma-Aldrich 8.00753 Sebacic acid for synthesis 111-20-6 50kg $1280 2024-03-01 Buy
Sigma-Aldrich 283258 Sebacic acid 99% 111-20-6 5g $56.6 2024-03-01 Buy
Product number Packaging Price Buy
8.00753 100g $32.6 Buy
8.00753 500g $91.4 Buy
8.00753 1kg $147 Buy
8.00753 50kg $1280 Buy
283258 5g $56.6 Buy

Sebacic acid Chemical Properties,Uses,Production

The main method of preparation

(1) Castor oil is as raw material, ricinoleate is separated from castor oil, with the condition of inflating and 280~300℃, caustic soda proceeds alkali fusion and the reaction is heated for 10h, sebum acid sodium salt can obtain, deputy product is 2-octanol. The sodium salt is dissolved in water, adding sulfuric acid to neutralize, after bleaching, the solution is cooled to precipitate sebum acid, it is washed with cold water, and finally recrystallized.
CH3 (CH2) 5CH (OH) CH2CH = CH (CH2) 7COOH +
2NaOH → CH3 (CH2) 5CH (OH) CH3 + NaOOC (CH2) 8COONa + H2
NaOOC (CH2) 3COONa + H2SO4 → HOOC (CH2) 8COOH + Na2SO4
(2) Adipic acid (hexane diacid) is as raw material to synthesize. Adipic acid and methanol can proceed esterification reaction to form dimethyl adipate, ion exchange membrane proceeds electrolytic oxidation to get dimer, i.e., dimethyl sebacate, and then reacts with sodium hydroxide to form the disodium salt, hydrochloric acid (or sulfuric acid) is used to neutralize and Sebacic acid can obtain.
Chemical properties, uses and methods of preparation of sebacic acid are edited by Chemicalbook andy.(2016-12-04)

Chemical properties

It is white flaky crystal. It is slightly soluble in water, soluble in alcohol and ether.

Uses

Sebacic acid is widely used in the preparation of sebacic acid esters, such as dibutyl sebacate, dioctyl sebacate, diisooctyl sebacate. These esters can be used as plasticizers for plastics and cold-resistant rubber, as well as for polyamide, polyurethane, alkyd resin, synthetic lubricating oil, lubricating oil additives, spices, coatings, cosmetics, etc. It can also be used as raw material for producing nylon 1010, nylon 910, nylon 810, nylon 610, nylon 9 and high temperature resistant lubricating oil diethylhexyl ester. It is also the raw material for the production of alkyd resins (used as surface coatings, plasticized nitrocellulose coatings, and urea resin varnishes) and polyurethane rubber, cellulose resins, vinyl resins, and synthetic rubber plasticizers, softeners, and solvents.

Production method

Almost all of the current industrial production of sebacic acid is using castor oil as raw material.
Castor oil cracking method: castor oil is heated under the action of alkali hydrolysis to generate ricinoleic acid sodium soap, and then add sulfuric acid acid to generate ricinoleic acid; in the presence of diluent cresol, add alkali heated to 260-280 ℃ for cracking to generate sebacic acid double sodium salt and secoctanol and hydrogen, cracked material diluted by water, heated and neutralized with acid, the double sodium salt into a monosodium salt; and then boiled with acid after decolorization of activated carbon neutralization solution. The monosodium salt of sebacic acid is turned into sebacic acid crystals, and then separated and dried to obtain the finished product.

Toxicity

Sebacic acid, also known as 1, 10-decanedioic acid, belongs to aliphatic dibasic acid. Sebacic acid was present in the leaves of flue-cured tobacco, burley tobacco and aromatic tobacco. Sebacic acid was white crystal in flake form at room temperature. Slightly soluble in water, sebacic acid was insoluble in benzene, petroleum ether, carbon tetrachloride. In contrast, sebacic acid was soluble in ethanol and ethyl ether. Irritant to the eyes, respiratory system and skin irritation, sebacic acid oral harmful. However, sebacic acid was low toxic and flammable.

Hazards & Safety Information

Category: Flammable liquid
Toxicity: grading toxicity
Acute oral toxicity-rat LD50: 14375 mg/kg; Oral-Mouse LD50: 6000 mg/kg
Flammability hazard characteristics: flammable, the fire discharges acrid smoke
Storage characteristics: Treasury ventilation low-temperature drying
Extinguishing agent: Dry powder, foam, sand, water

Description

Sebacic acid is a dicarboxylic acid with structure (HOOC)(CH2)8(COOH), and is naturally occurring.
In its pure state it is a white flake or powdered crystal. The product is described as non-hazardous, though in its powdered form it can be prone to flash ignition (a typical risk in handling fine organic powders).
Sebaceus is Latin for tallow candle, sebum (tallow) is Latin for tallow, and refers to its use in the manufacture of candles. Sebacic acid is a derivative of castor oil, with the vast majority of world production occurring in China which annually exports over 20,000 metric tonnes, representing over 90 % of global trade of the product.
In the industrial setting, sebacic acid and its homologues such as azelaic acid can be used in plasticizers, lubricants, hydraulic fluids, cosmetics, candles, etc. Sebacic acid is also used as an intermediate for aromatics, antiseptics, and painting materials.

Chemical Properties

White flaky crystals. Slightly soluble in water, soluble in alcohol and ether.

Uses

Sebacic Acid is a urinary metabolite that has been identified as an anti-fatigue biomarker.

Uses

Decanedioic acid was named by Thenard LJ (1802) from the Latin sebaceus(tallow candle) or sebum (tallow) in reference to its use in the manufacture of candles. Thenard LJ isolated this compound from distillation products of beef tallow. In 1954, it was reported that it was produced in excess of 10,000 tons annually by alkali fission of castor oil. Sebacic acid and its derivatives, as azelaic acid, have a variety of industrial uses as plasticizers, lubricants, diffusion pump oils, cosmetics, candles, etc. It is also used in the synthesis of polyamide, as nylon, and of alkyd resins. An isomer, isosebacic acid, has several applications in the manufacture of vinyl resin plasticizers, extrusion plastics, adhesives, ester lubricants, polyesters, polyurethane resins and synthetic rubber.

Definition

ChEBI: Sebacic acid is an alpha,omega-dicarboxylic acid that is the 1,8-dicarboxy derivative of octane. It has a role as a human metabolite and a plant metabolite. It is an alpha,omega-dicarboxylic acid and a dicarboxylic fatty acid. It is a conjugate acid of a sebacate(2-) and a sebacate. It derives from a hydride of a decane.

Preparation

Sebacic acid is normally made from castor oil, which is essentially glycerol triricinoleate. The castor oil is heated with sodium hydroxide at about 250??e. This treatment results in saponification of the castor oil to ricinoleic acid which is then cleaved to give 2-octanol and sebacic acid:

111-20-6 synthesis


This process results in low yields of sebacic acid (about 50% based on the castor oil) but, nevertheless, other routes have not proved competitive. Sebacic acid is a colourless crystalline solid, m.p. 134??.

General Description

White granular powder. Melting point 153°F. Slightly soluble in water. Sublimes slowly at 750 mm Hg when heated to melting point.

Air & Water Reactions

Insoluble in water.

Reactivity Profile

Sebacic acid reacts exothermically to neutralize bases, both organic and inorganic. May react rapidly with aqueous solutions containing a chemical base and dissolve as the neutralization generates a soluble salt. Can react with active metals to form gaseous hydrogen and a metal salt. Such reactions are slow in the dry, but systems may absorb enough water from the air to allow corrosion of iron, steel, and aluminum parts and containers. Reacts slowly with cyanide salts to generate gaseous hydrogen cyanide. Reacts with solutions of cyanides to cause the release of gaseous hydrogen cyanide. May generate flammable and/or toxic gases and heat with diazo compounds, dithiocarbamates, isocyanates, mercaptans, nitrides, and sulfides. May react with sulfites, nitrites, thiosulfates (to give H2S and SO3), dithionites (SO2), to generate flammable and/or toxic gases and heat. Can be oxidized exothermically by strong oxidizing agents and reduced by strong reducing agents. May initiate polymerization reactions.

Fire Hazard

Flash point data for Sebacic acid are not available. Sebacic acid is probably combustible.

Flammability and Explosibility

Not classified

Purification Methods

Purify sebacic acid via the disodium salt which, after crystallisation from boiling water (charcoal), is again converted to the free acid. The free acid is crystallised repeatedly from hot distilled water or from Me2CO/pet ether and dried under vacuum. [Beilstein 2 IV 2078.]

5169-82-4
111-20-6
Synthesis of Sebacic acid from Decanedioic acid, 4,7-dioxo-
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View Lastest Price from Sebacic acid manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Decanedioic acid pictures 2024-11-05 Decanedioic acid
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US $86.00 / g 99% 10g TargetMol Chemicals Inc.
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US $99.00-35.00 / kg 1kg 99% 5000 ton Hebei Zhuanglai Chemical Trading Co.,Ltd
Sebacic acid pictures 2024-11-05 Sebacic acid
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US $100.00-75.00 / kg 1kg 99% 5000Ton HEBEI SHENGSUAN CHEMICAL INDUSTRY CO.,LTD
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  • Sebacic Acid
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  • US $99.00-35.00 / kg
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  • Hebei Zhuanglai Chemical Trading Co.,Ltd
  • Sebacic acid pictures
  • Sebacic acid
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  • US $100.00-75.00 / kg
  • 99%
  • HEBEI SHENGSUAN CHEMICAL INDUSTRY CO.,LTD
RARECHEM AL BO 0380 SEBACIC ACID SEBACINIC ACID 1,10-decanedioicacid Ipomic acid n-decanedioicacid 1,8-OctanedicarbozylicAcid SebacicAcidForSynthesis SebacicAcid,>95% Sebacic acid, 98+% SEBCIC ACID Decanedioic SEBACICACID,REAGENT Sebacinsure octane dicarboxylic acid Sebacic acid,90%,pract. Sabacic acid Sebacic acid, 98% 100GR Decanedioic Acid 1,8-Octanedicarboxylic Acid 1.8-Octanedica Sebacic acid >=95.0% (GC) Dicarboxylic acid C10 Octane-1,8-dicarboxylicacid sebacinsaure Sebacylicacid Seracic acid usafhc-1 SEBACIC ACID MIN 98% Sebacic acid≥ 99% (Titration) Sebacic Acid > SEBACIC ACID FOR SYNTHESIS 100 G SEBACIC ACID FOR SYNTHESIS 1 KG SEBACIC ACID FOR SYNTHESIS 50 KG SEBACIC ACID FOR SYNTHESIS 500 G DecanedioicacidCAS: DECANEDIOIC ACID 1,8-OCTANEDICARBOXYLIC ACID 1,10-Decanedioic acid acidesebacique Decanedicarboxylic acid n-Decanedioic acid SEBACIC ACID pure sebacic USAF hc-1 sebacate (decanedioate) Sebacic acidTAINS CA. 35% MONOPALMITATE) 1,8-Octanedicarboxylic Acid (Decanedioic Acid) Nandrolone Decanoate Impurity 13 111-20-6 11/20/2006 11-20-6 CH28COOH2 COCHCH28COOH HO2CCH28CO2H HOOCCH28COOH Building Blocks Carboxylic Acids Carbonyl Compounds