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TALLOW ALCOHOL

Tallow alcohol is a Mixt of fatty alcohols derived from tallow Tallow alcohol uses and applications include: Emollient, emulsifier, consistency agent, cosolvent for cosmetics, skin creamslotions; defoamer;in paperpaperboard in contact with aqueousfatty foods.Waxy white solid with a mild soapy odor. Floats on water.

CAS NO:99561-04-3
EC NO:308-980-4

SYNONYMS
alcohols, tallow;Alkohole, Talg;tallow alcohols;İÇ YAĞI ALKOLU;içyağı alkolü;Einecs 308-980-4

SYNONYMS
alcohols, tallow;Alkohole, Talg;tallow alcohols;İÇ YAĞI ALKOLU;içyağı alkolü;Einecs 308-980-4;Alcohols, tallow;Alkohole, Talg;tallow alcohols;Einecs 308-980-4;Alcohols, tallow;99561-04-3;Alcohols, tallow;EINECS 308-980-4

Tallow alcohol is a Mixt of fatty alcohols derived from tallow Tallow alcohol uses and applications include: Emollient, emulsifier, consistency agent, cosolvent for cosmetics, skin creamslotions; defoamer;in paperpaperboard in contact with aqueousfatty foods.Waxy white solid with a mild soapy odor. Floats on water.

Organoleptic Properties:
Odor and/or flavor descriptions from others (if found).
 
Cosmetic Information:
Cosing:    cosmetic data
Cosmetic Uses:    emollients
emulsifying agents
emulsion stabilisers
refatting agents
viscosity controlling agents

Potential Uses:
 emollients
 emulsifying agents

Tallow alcohol is a Mixt. of fatty alcohols derived from tallow Tallow alcohol uses and applications include: Emollient, emulsifier, consistency agent, cosolvent for cosmetics, skin creamslotions; defoamer; in paperpaperboard in contact with aqueousfatty foods

Properties

Appearance , solid.

Solubility    insoluble in water.

Stability    stable. Easily oxidized.

Risk    Solid form: flammable material; irritation, irritation to skin, eye, respiratory system. Harmful products of combustion are CO, CO2 and so on. Contact with strong oxidants, can cause to burn.

Ecology    may be hazardous to environment. Water body should be given special attention.

Biodegradability    biodegradable.

Characteristics    excellent dispersing, emulsifying, lubricating, solubilizing abilities.

Synthesis

Quality Standards & Test Methods

1, Physical and chemical indexes

Physical and chemical indexes

Solid

Actives, %,C 95.0

Test Methods

Actives

GB/T 13173 Surface active agents - Detergents - Testing methods

2, Hazardous substances indexes

Item

Hazardous substances indexes

Solid

Heavy metals (as Pb), mg/Kg,C 20

As, mg/Kg,C 3

Test Methods

Heavy metals (as Pb)

Safety and Technical Standards for Cosmetics 

GB/T 30799 The test method of food detergents - Determination of heavy metals as

Safety and Technical Standards for Cosmetics

GB/T 30797 The test method of food detergents - Determination of total arsenic

3, Further explanation

(a), On physical and chemical indexes: firstly, shall be indicated carbon atom distribution; secondly, shall be indicated average molecular weight.

(b), Used in cosmetics, should be test for harmful substances or furtherly test for microorganisms, according to local regulations and standards.

Major Uses

1, Typical applications

Use as dispersing agent, emulsifying agent.

Use as lubricant.

Use as intermediate in organic synthesis.

2, Personal care products

Conditioning agent, emollient, viscosity controlling agent, emulsifying agent, emulsion stabilizer, refatting agent in personal care products.

Production and occurrence
Most fatty alcohols in nature are found as waxes which are esters with fatty acids and fatty alcohols.They are produced by bacteria, plants and animals for purposes of buoyancy, as source of metabolic water and energy, biosonar lenses (marine mammals) and for thermal insulation in the form of waxes (in plants and insects).Fatty alcohols were unavailable until the early 1900s. They were originally obtained by reduction of wax esters with sodium by the Bouveault–Blanc reduction process. In the 1930s catalytic hydrogenation was commercialized, which allowed the conversion of fatty acid esters, typically tallow, to the alcohols. In the 1940s and 1950s, petrochemicals became an important source of chemicals, and Karl Ziegler had discovered the polymerization of ethylene. These two developments opened the way to synthetic fatty alcohols.

From natural sources
The traditional sources of fatty alcohols have largely been various vegetable oils and these remain a large-scale feedstock. Animal fats (tallow) were of historic importance, particularly whale oil, however they are no longer used on a large scale. Tallows produce a fairly narrow range of alcohols, predominantly C16–C18, the chain lengths from plant sources are more variable (C6–C24) making them the preferred source. The alcohols are obtained from the triglycerides (fatty acid triesters), which form the bulk of the oil. The process involves the transesterification of the triglycerides to give methyl esters which are then hydrogenated to give the fatty alcohols.Higher alcohols (C20–C22) can be obtained from rapeseed oil or mustard seed oil. Midcut alcohols are obtained from coconut oil (C12–C14) or palm kernel oil (C16–C18)

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