CAPRIC ALCOHOL

PRODUCT IDENTIFICATION
CAS NO. 112-30-1, 36729-58-5

CAPRIC ALCOHOL
EINECS NO. 203-956-9, 253-173-1
FORMULA CH3(CH2)8CH2OH
MOL WT. 158.28
H.S. CODE 2905.17

TOXICITY

  
SYNONYMS Caprinic alcohol; Decanol; Nonylcarbinol; Decylic Alcohol;
1-Decanol; Alcohol C-10; Decan-1-ol; Decyl alcohol; decanol; n-Decyl Alcohol; Nonyl acarbinol;

DERIVATION

 

CLASSIFICATION

 

PHYSICAL AND CHEMICAL PROPERTIES
PHYSICAL STATE clear oily liquid
MELTING POINT 5 - 7 C
BOILING POINT 231 C
SPECIFIC GRAVITY 0.825 - 0.835
SOLUBILITY IN WATER Insoluble
pH

 
VAPOR DENSITY 5.46
AUTOIGNITION

255 C
NFPA RATINGS Health: 21; Flammability: 2; Reactivity: 0

REFRACTIVE INDEX

  
FLASH POINT

82 C
STABILITY Stable under ordinary conditions

GENERAL DESCRIPTION AND APPLICATIONS
Fatty alcohols, derived from natural fats and oils, are high molecular straight chain primary alcohols. They include lauryl (C12), MyrIstyl (C14), Cetyl ( or palmityl: C16), stearyl (C18), Oleyl (C18, unsaturated), and Linoleyl (C18, polyunsaturated) alcohols. There are synthetic fatty alcohols equivalent physically and chemically to natural alcohols obtained from oleochemical sources such as coconut and palm kernel oil. Fatty alcohols are emulsifiers and emollients to make skin smoother and prevent moisture loss. Identical fatty esters are used to improve rub-out of formulas and to control viscosity and dispersion characteristics in cosmetics, personal care products and pharmaceutical ingredients. As chemical intermediates, the primary use of fatty alcohols are as raw material for the production of fatty sulfate salts and alcohol ethoxylates for foaming and cleaning purposes in the field of detergent industry. Chemical reactions of primary alcohols include esterifications, ethoxylation, sulfation, oxidation and many other reactions. Their derivatives and end use applications include;
  • Nonionic surfactants (Ethoxylates and propoxylates)
  • Anionic surfactants (Alkyl sulfates and alkyl ethoxy sulfates)
  • Chemical intermediates and  polymerization modifiers (Alkyl halides, Alkyl mercaptans)
  • Quaternary ammonium compounds for detergent sanitisers, softner for textiles, phase transfer catalyst and biocides
  • Antioxidants for plastics (Alkyl thiopropionates and alkyl phosphites)
  • Lubricant additives (Metallic and thio alkylphosphates)
  • Flavor and Fragrance (Aldehydes and ketones)
  • PVC plasticizers (Dialkyl Phthalates, adipates and trimellitates)
  • Coatings and inks (acrylate and methacrylate esters)
  • Water treatment (acrylate and methacrylate esters)

Large amount of fatty alcohols are used as special solvents, fillers in plasticizer and insulating materials for the building industry. Fatty alcohols are used as ingredients in the industries of agricultural, foodstuff, metal processing, cosmetics, lube additive, pharmaceutical, rubber, textile, perfume and flavouring as well as synthetic detergent.

LSALES SPECIFICATION

APPEARANCE

 clear oily liquid

TOTAL ALCOHOL

99.5% min
IODINE VALUE 0.1 max

ACID VALUE

0.1 max

SAP VALUE

0.5 max

HYDROXYL VALUE

351 - 356

SOLIDIFICATION

4 - 7 C

COLOR, APHA

10 max

WATER

0.1% max

C DISTRIBUTION

C8 (2.0% max) + C10 (98.0% min) + C12 (2.0% max)
TRANSPORTATION
PACKING 160kgs in drum
HAZARD CLASS 9 (Packing Group: III)
UN NO. 3082
OTHER INFORMATION
Hazard Symbols: XI N, Risk Phrases: 20-36/37/38-51/53, Safety Phrases: 26-60

GENERAL DESCRIPTION OF FATTY ACID
Fatty Acids are aliphatic carboxylic acid with varying hydrocarbon lengths at one end of the chain joined to terminal carboxyl (-COOH) group at the other end. The general formula is R-(CH2)n-COOH. Fatty acids are predominantly unbranched and those with even numbers of carbon atoms between 12 and 22 carbons long react with glycerol to form lipids (fat-soluble components of living cells) in plants, animals, and microorganisms. Fatty acids all have common names respectively lilk lauric (C12), MyrIstic (C14), palmitic (C16), stearic (C18), oleic (C18, unsaturated), and linoleic (C18, polyunsaturated) acids. The saturated fatty acids have no double bonds, while oleic acid is an unsaturated fatty acid has one double bond (also described as olefinic) and polyunsaturated fatty acids like linolenic acid contain two or more double bonds. Lauric acid (also called Dodecanoic acid) is the main acid in coconut oil (45 - 50 percent) and palm kernel oil (45 - 55 percent). Nutmeg butter is rich in myristic acid (also called Tetradecanoic acid ) which constitutes 60-75 percent of the fatty-acid content. Palmitic acid(also called Hexadecylic acid ) constitutes between 20 and 30 percent of most animal fats and is also an important constituent of most vegetable fats (35 - 45 percent of palm oil). Stearic acid ( also called Octadecanoic Acid)  is nature's most common long-chain fatty acids, derived from animal and vegetable fats. It is widely used as a lubricant and as an additive in industrial preparations. It is used in the manufacture of metallic stearates, pharmaceuticals, soaps, cosmetics, and food packaging. It is also used as a softener, accelerator activator and dispersing agent in rubbers. Oleic acid (systematic chemical name is cis-octadec-9-enoic acid) is the most abundant of the unsaturated fatty acids in nature.
  • SATURATED FATTY ACIDS

COMMON NAME

SYSTEMATIC NAME

CAS RN

Length

MELTING POINT

Undecylic Acid

 n-Hendecanoic Acid 112-37-8 Straight 11:0

30 C
Lauric Acid n-Dodecanoic Acid 143-07-7 Straight 12:0

44 C

Tridecylic Acid

n-Tridecanoic Acid

 638-53-9 Straight 13:0

42 C
Myristic Acid n-Tetradecanoic Acid 544-63-8 Straight 14:0

54 C
Pentadecanoic Acid n-Pentadecanoic Acid 1002-84-2 Straight 15:0

52 C
Palmitic Acid n-Hexadecanoic Acid 57-10-3 Straight 16:0

62 C

Margaric Acid

n-Heptadecanoic Acid

 506-12-7 Straight 17:0

61 C
Stearic Acid n-Octadecanoic Acid 57-11-4 Straight 18:0

70 C

Nondecylic Acid

n-Nonadecanoic Acid

 646-30-0 Straight 19:0

70 C
Arachidic Acid n-Eicosanoic Acid 506-30-9 Straight 20:0

75 C
Henicosanoic acid

n-Heneicosanoic Acid

 2363-71-5 Straight 21:0

74 C
Behenic Acid

n-Docosanoic Acid

 112-85-6 Straight 22:0

81 C
Tricosanoic acid n-Tricosanoic acid 2433-96-7 Straight 23:0

80 C
Lignoceric Acid n-Tetracosanoic Acid 557-59-5 Straight 24:0

85 C

Pentacosanoic Acid

n-Pentacosanoic Acid

 506-38-7 Straight 25:0

85 C
Cerotinic acid n-Hexacosanoic acid 506-46-7 Straight 26:0

87 C

Heptacosanoic Acid

n-Heptacosanoic Acid

 7138-40-1 Straight 27:0

87 C
Montanic acid n-Octacosanoic acid 506-48-9 Straight 28:0

91 C

Nonacosanoic Acid

n-Nonacosanoic Acid

 4250-38-8 Straight 29:0

91 C
Melissic acid n-Triacontanoic acid 506-50-3 Straight 30:0

93 C
 

n-Hentriacontanoic Acid

 38232-01-8 Straight 31:0

 

Lacceroic Acid

 n-Dotriacontanoic Acid

 

 Straight 32:0

 
Ceromelissic Acid n-Tritriacontanoic acid

 

 Straight 33:0

 
Geddic Acid n-Tetratriacontanoic acid

 

 Straight 34:0

 
Ceroplastic Acid n-Pentatriacontanoic acid

 

 Straight 35:0