LAURYL ALCOHOL 70%

CAS No:112-53-8

Synonyms:
Dodecyl alcohol;n-Dodecan-1-ol;n-Dodecanol;n-Dodecyl alcohol;Alcohol C-12;Alfol 12;CO 12;Dodecanol-1;Dytol J-68;Karukoru 20;Lauric Alcohol;Laurinic alcohol;Lauryl alcohol;Lauryl 24;Pisol;S 1298;Sipol L12;Siponol L2;Siponol L5;Siponol 25;1-Dodecyl Alcohol;Duodecyl alcohol;n-Lauryl alcohol;Dodecan-1-ol;Cachalot l-50;Cachalot l-90;Co-1214S1-dodecanol;Lorol;Lorol 11;Lorol 5;Lorol 7;CO-1214;CO-1214N;CO-1214S;Epal 12;n-Lauryl alcohol, primary;MA-1214;D; Dodecanol; n-Dodecanol; lauryl alcohol; Dodecan-1-ol; Dodecyl alcohol; n-Dodecan-1-ol; n-Dodecyl alcohol; Alcohol C-12; Alfol 12; Dodecanol-1; Dytol J-68; Karukoru 20; Lauric Alcohol; Laurinic alcohol; Lauryl 24; Pisol; S 1298; Sipol L12; Siponol L2; Siponol L5; Siponol 25; 1-Dodecyl Alcohol; Duodecyl alcohol; n-Lauryl alcohol; Cachalot l-50; Cachalot l-90; Lorol 11; Lorol 5; Lorol 7; CO-1214; CO-1214N; CO-1214S; Epal 12; n-Lauryl alcohol, primary; MA-1214; 1-Hydroxydodecane; Hydroxydodecane; Lorol C12; Undecyl carbinol; Adol 10; Adol 12; NAA 42; Nacol 12-96; Hainol 12SS; Conol 20P; Conol 20PP; 1322-35-6; 68855-55-0; 8014-32-2; 8032-08-4; 8032-09-5; 1-Dodecanol, Alcohol C12, Dodecyl alcohol, Lauryl alcohol;Alcohol C12, Dodecyl alcohol, Lauryl alcohol;Fatty Acid Derivatives; CS-AE-00084; DODECYL 112-53-8; 186.3342; C12H26O;Hydroxydodecane; Undecyl carbinol;Alcohol C12;oleachemicals;fatty acid;FATTY ACID;OLEACHEMICALS;Dodécane-1-ol (French);;1-DODECANOL;Dodecyl alcohol;Lauryl alcohol;Dodecan-1-ol;Dodecanol;112-53-8;n-Dodecyl alcohol;Lauric alcohol;Laurinic alcohol;Undecyl carbinol;1-Dodecyl alcohol;Pisol;n-Dodecan-1-ol;n-Dodecanol;Duodecyl alcohol;1-Hydroxydodecane;Siponol L5;Karukoru 20;Siponol 25;Lorol 5;Lorol 7;Lauryl 24;Alcohol C-12;Alfol 12;Lorol 11;Sipol L12,Dytol J-68;Siponol L2;Dodecylalcohol;Cachalot L-50;Cachalot L-90;Lauroyl alcohol;n-Lauryl alcohol;C12 alcohol;Hainol 12SS;Hydroxydodecane;Conol 20P;Conol 20PP;Lorol;EPAL 12;Adol 10;Adol 12;Dodecanol-1;n-Lauryl alcohol, primary;Nacol 12-96;Alcohols, C8-18;Fatty alcohol(C12);Adol 11;Lorol C 12;NAA 42;FEMA Number 2617;Dytol J-68 (VAN);Lorol C 12/98;CO-1214N;CO-1214S;Alcohol C12;CCRIS 662;Dodecanol, 1-;S 1298;UNII-178A96NLP2;CO-1214;MA-1214;FEMA No. 2617;Lorol C12;HSDB 1075,NSC 3724;Co-1214S1-dodecanol;EINECS 203-982-0;EPA Pesticide Chemical Code 001509;BRN 1738860;AI3-00309;CHEBI:28878;LQZZUXJYWNFBMV-UHFFFAOYSA-N;MFCD00004753;SBB008734;DSSTox_CID_6918;DSSTox_RID_78253;DSSTox_GSID_26918;27342-88-7;68551-07-5;1DO;CAS-112-53-8;C8-18 Alcohols;75782-86-4;Fatty (C8-C18) alcohol;laurylalcohol;Dodecyl alcoho;Lorol special;Lipocol L;EINECS 271-359-0;Philcohol 1200;Lorol C8-C10 special;AC1Q7CPX;Lorol C12-C14;1-Dodecanol, 98.0%;AC1L1QH4;AC1Q2W6M;SCHEMBL6844;ACMC-1C59L;4-01-00-01844 ;KSC175C0L;CHEMBL24722;WLN: Q12;Lauryl alcohol, >=98%, FG;1-Dodecanol, 98% 250g;DTXSID5026918;1-dodecanol (ACD/Name4.0);1-Dodecanol, analytical standard;CTK0H5105;HMDB11626;NSC3724;MolPort-001-779-974;178A96NLP2;1-Dodecanol, reagent grade, 98%;CS-D1360;NSC-3724;ZINC1529403;Tox21_202124;Tox21_300120;ANW-16485;LMFA05000001;STL301829;Co 12Co-1214Co-1214N;AKOS009031450;DB06894;LS-2878;MCULE-9381688904;NE10351;RTR-002445;TRA0037635;1-Dodecanol, ACS reagent, >=98.0%;NCGC00164341-01;NCGC00164341-02;NCGC00164341-03;NCGC00253987-01;NCGC00259673-01;AN-43138;KB-12051;LP003195;DB-003637;TR-002445;1-Dodecanol, SAJ special grade, >=97.0%;1-Dodecanol, Selectophore(TM), >=98.0%;D0978;FT-0607710;FT-0619169;FT-0638555;FT-0638873;FT-0693265;Oxo alcohol still bottoms(C8-18 alcohols);ST51046177;1-Dodecanol, Vetec(TM) reagent grade, 98%;EN300-20043;C02277;Q-200121;I14-17885;I14-59074;I14-94627;3B1-001845;UNII-2C8M6XLB5C component LQZZUXJYWNFBMV-UHFFFAOYSA-N;UNII-B1K89384RJ component LQZZUXJYWNFBMV-UHFFFAOYSA-N;UNII-S4827SZE3L component LQZZUXJYWNFBMV-UHFFFAOYSA-N;UNII-T7ZJT3I9X2 component LQZZUXJYWNFBMV-UHFFFAOYSA-N;Lauryl alcohol, United States Pharmacopeia (USP) Reference Standard;1173838-88-4;322-35-6;68855-55-0;8014-322;8032-08-4;8032-09-5;8032-10-8;LAURYL ALCOHOL, 1-HYDROXYDODECANE; DIDECYL ALCOHOL; DODECAN-1-OL; ALCOHOL C-12; ALFOL 12; CACHALOT L-50; CACHALOT L-90; CO 12; CO-1214; CO-1214N; CO-1214S;Oleochemicals: Fatty Acids, Fatty Alcohol & more , Industrial Chemicals , Green Chemicals - Eco-Friendly , Dodecan-1-ol;112-53-8 [RN];1-Dodecanol [ACD/Index Name] [ACD/IUPAC Name],1-Dodecanol [German] [ACD/Index Name] [ACD/IUPAC Name];-Dodécanol [French] [ACD/IUPAC Name];1-Dodecyl alcohol;1-Hydroxydodecane;203-982-0 [EINECS];278-306-0 [EINECS];DODECANOL [Wiki];Dodecyl alcohol;Hydroxydodecane;Lauryl Alcohol;n-Dodecanol;n-Lauryl alcohol;1,1-DIDEUTERO-1-DODECANOL;178A96NLP2;264-118-6 [EINECS];272-490-6 [EINECS];4-01-00-01844 (Beilstein Handbook Reference) [Beilstein];4-01-00-01864 (Beilstein Handbook Reference) [Beilstein];4-01-00-01876 (Beilstein Handbook Reference) [Beilstein];4-01-00-01888 [Beilstein];Adol 52 NF [NF];Adol 52NF;AIDS471017;AIDS-471017;Alcohol stearylicus;AtalcozC;Atalco S;Cetaffine,CETAL;Cetalol CA;Cetyl alcohol [NF],Conol 20P;Conol 20PP,Crodacol C;Crodacol-CAS;Crodacol-CAT;Crodacol-S;Dodecan-1-al;Dodecanol, 1-;dodecyl-1-ol;Duodecyl alcohol;Dytol F-11;Dytol J-68 (VAN);Dytol R-52;Elfacos C;Ethal ;Ethol;Exxal 12;Hainol 12SS;Hyfatol;Hyfatol 16;Karukoru 20;Lanette K;Lanette Wax KS;Lanol C;Lanol S;Lauric alcohol;Laurinic alcohol,Lauroyl alcohol,LAURYL ALCOHOL[11,12-3H];Lipocol L;LMFA05000061;Lorol;Lorol C 12;Lorol C12;Lorol special,Loxanol K;Loxanol K extra;LOXANOLV;Loxanwachs SK;Nacol 12-96;n-Cetyl alcohol;n-Dodecan-1-ol,n-dodecanol|dodecyl alcohol|dodecan-1-ol|lauric alcohol|lauryl alcohol|laurinic alcohol|lorol;N-DODECYL ALCOHOL;Pisol;Polaax;Q12 [WLN];Sipol L12;SipolS;Siponol CC;Siponol L2;Siponol L5;Siponol S;Siponol SC;Siponol wax-A;SSD AF;SSD RP;stenol,Steraffine;Undecyl carbinol;UNII:178A96NLP2;USP XIII stearyl alcohol [USP],WLN: Q12;十二烷醇 [Chinese];co12;CO 12;Lorol;Pisol;s1298;epal12;lauryl;lorol5;lorol7;S 1298Dodecyl gallate; Tetradecanedioic acid; TRIDECANOIC ACID; PALMITIC ACID; SODIUM SALT; AGARIC ACID; 12-HYDROXYDODECANOIC ACID; 4-Dodecyloxybenzoic acid; 1,11-Undecanedicarboxylic acid; HEXADECANOIC ACID-1-13C; HEXADECANEDIOIC ACID; Dodecanedioic acid; 11-CYANO-1-UNDECANOIC ACID; 12-Bromododecanoic acid; PENTADECANOIC ACID; Myristic acid; 4-HEXADECYLOXYBENZOIC ACID; Palmitic acid; DODECANOIC ACID-1-13C;RARECHEM AL BD 0157; TIMTEC-BB; SBB008734; N-DODECYL ALCOHOL; Fatty Acids; Fatty Alcohols; Oxygen Compounds; Saturated fatty acids derivatives; Lipids Organic Building Blocks; 1-Hydroxydodecane; Alfol 12; alfol12 ;Cachalot l-50; Cachalot l-90; cachalot l-50; cachalotl-90; CO 12; co12; CO-1214; CO-1214N; CO-1214S; Co-1214S1-dodecanol; Didecylalcohol; dodecan-1- dodecanol(non-specificname); Dodecanol-1 dodecyl; Dodecylalkohol; Duodecyl alcohol; duodecylalcohol; Dytol J-68; dytolj-68; Emery 3326; Emery 3332; Emery 3357; Epal 12; epal12; Exxal 12; Fatty alcohol; femanumber2617; Hydroxydodecane; Karukoru 20; karukoru20; Lauric Alcohol; lauricalcohol; Laurinic alcohol; laurinicalcohol;lauryl; Lauryl 24; lauryl24; Lipocol; L Lorol; Lorol 11; Lorol 5 ;Lorol 7; Lorol C12; Lorol C12-C14; Lorol C8-C10 special;(US EPA PC Code ) , (US EPA PC Code ) , 001509 (US EPA PC Code Text ) , 1-Dodecanol , 1-Hydroxydodecane , 112-53-8 (CAS number) , 112538 , 112538 (CAS number without hyphens) , 2343 (CA DPR Chem Code) ) , 27342-88-7 (CAS number) , 27342887 (CAS number without hyphens) , 900284 (US EPA PC Code Text ) , Alcohol, C12 , çlcool Laur?lico , çlcoolLaur?lico , Codling moth pheromone , dodecan-1-ol , Dodecanol , Dodecyl alcohol , Hickory shuckworm phereomone , Lauryl alcohol , LAURYL ALCOHOL (CA DPR Chem Code Text ) , Laurylalcohol , Oblique-banded leafroller pheromone;1-Dodecanol; Dodecyl alcohol; n-Dodecan-1-ol; n-Dodecanol; n-Dodecyl alcohol; Alcohol C-12; Alfol 12; CO 12; Dodecanol-1; Dytol J-68; Karukoru 20; Lauric Alcohol; Laurinic alcohol; Lauryl alcohol; Lauryl 24; Pisol; S 1298; Sipol L12; Siponol L2; Siponol L5; Siponol 25; 1-Dodecyl Alcohol; Duodecyl alcohol; n-Lauryl alcohol; Dodecan-1-ol;LIPOCAL;lipocal;Dodecan-1-ol;Cachalot l-50;Cachalot l-90;Co-1214S1-dodecanol;Lorol;Lorol 11;Lorol 5;Lorol 7;CO-1214;CO-1214N;CO-1214S;Epal 12;n-Lauryl alcohol, primary;MA-1214;D;Alkoxylates;Ether sulfates;esters;Sulfates; Ethoxylates;Lauril ALKOL;loril alkol;Lauril alkol;LAURİL ALKOL;lauril alkol;Lauryl alcohol prices;lauryl alcohol suppliers.; 1-DODECANOL; Dodecan-1-ol;lauril alkol; Dodecyl alcohol; Lauryl alcohol; 112-53-8; n-Dodecyl alcohol; Undecyl carbinol; Dodecylalcohol; Lauric alcohol; Laurinic alcohol; 1-Dodecyl alcohol; Pisol; n-Dodecan-1-ol; Duodecyl alcohol; 1-Hydroxydodecane; Siponol L5; Karukoru 20; Lauroyl alcohol; Siponol 25; lauril alkol;lauril alkole; louroyl alcohol; lauroil alcohol; lauril alcohol; lauryle alcohole;  Dodecanol; 1-Dodecanol

Lauryl alcohol 70%

Lauryl alcohol

Dodecanol[1]
Skeletal formula
Space-filling model
Names
IUPAC name
Dodecan-1-ol
Other names
Lauryl alcohol
1-Dodecanol
Dodecyl alcohol
Lauryl alcohol
Identifiers
CAS Number    
112-53-8 ☑
3D model (JSmol)    
Interactive image
ChEBI    
CHEBI:28878 ☑
ChEMBL    
ChEMBL24722 ☑
ChemSpider    
7901 ☑
DrugBank    
DB06894 ☑
ECHA InfoCard    100.003.620
KEGG    
C02277 ☑
PubChem CID    
8193
UNII    
178A96NLP2 ☑
CompTox Dashboard (EPA)    
DTXSID5026918 Edit this at Wikidata
InChI[show]
SMILES[show]
Properties
Chemical formula    C12H26O
Molar mass    186.34
Appearance    Colorless solid
Density    0.8309
Melting point    24 °C (75 °F; 297 K)
Boiling point    259 °C (498 °F; 532 K)
Solubility in water    0.004 g/L[2]
Solubility in ethanol and diethyl ether    Soluble
Magnetic susceptibility (χ)    -147.70·10−6 cm3/mol
Related compounds
Related    
Dodecanal
Dodecanoic acid
1-Bromododecane
Hazards
R/S statement (outdated)    R36
Flash point    127 °C (261 °F; 400 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references
Lauryl alcohol /ˈdoʊˈdɛkɑːnɒl/, or lauryl alcohol, is an organic compound produced industrially from palm kernel oil or coconut oil. It is a fatty alcohol. Sulfate esters of lauryl alcohol, especially sodium lauryl sulfate, are very widely used as surfactants. Sodium lauryl sulfate, ammonium lauryl sulfate, and sodium laureth sulfate are all used in shampoos. Lauryl alcohol is tasteless and colorless with a floral odor.[3]

Production and use
In 1993, the European demand of Lauryl alcohol was around 60 thousand tons per year (Tt/a). It can be obtained from palm kernel or coconut oil fatty acids and methyl esters by hydrogenation.[4] It may also be produced synthetically via the Ziegler process. A classic laboratory method involves Bouveault-Blanc reduction of ethyl laurate.[3]

Lauryl alcohol is used to make surfactants, lubricating oils, pharmaceuticals, in the formation of monolithic polymers and as a flavor enhancing food additive. In cosmetics, Lauryl alcohol is used as an emollient. It is also the precursor to dodecanal, an important fragrance, and 1-bromododecane, an alkylating agent for improving the lipophilicity of organic molecules.

Toxicity
Lauryl alcohol can irritate the skin. It has about half the toxicity of ethanol, but it is very harmful to marine organisms.[5]

Mutual solubility with water
The mutual solubility of 1-Lauryl alcohol and water has been quantified as follows.[6]

Mutual Solubility of Water and 1-Dodecanol (98%, Melting Point 24 °C), Weight %
Temperature, °C    Solubility of Lauryl alcohol in Water    Solubility of Water in Lauryl alcohol
29.5    0.04    2.87
40.0    0.05    2.85
50.2    0.09    2.69
60.5    0.15    2.96
70.5    0.09    2.70
80.3    0.14    2.89
90.8    0.18    2.96
standard deviation    0.02    0.01

Lauryl alcohol is a saturated 12-carbon fatty alcohol obtained from coconut oil fatty acids. It has a floral odor and is used in detergents, lubricating oils, and pharmaceuticals. (From McGraw-Hill Dictionary of Scientific and Technical Terms, 5th ed)

DrugBank
Lauryl alcohol, also known as dodecyl alcohol or lauryl alcohol, belongs to the class of organic compounds known as fatty alcohols. These are aliphatic alcohols consisting of a chain of a least six carbon atoms. Thus, is considered to be a fatty alcohol lipid molecule. exists as a solid and is considered to be practically insoluble (in water) and relatively neutral. has been detected in multiple biofluids, such as feces, saliva, and urine. Within the cell, is primarily located in the membrane (predicted from logP) and cytoplasm. exists in all eukaryotes, ranging from yeast to humans. participates in a number of enzymatic reactions. In particular, can be biosynthesized from dodecane. can also be converted into lauryl palmitoleate and dodecyl palmitate. Outside of the human body, can be found in a number of food items such as arrowhead, chickpea, narrowleaf cattail, and red rice. This makes a potential biomarker for the consumption of these food products.

Human Metabolome Database (HMDB)
Lauryl alcohol is a fatty alcohol that is dodecane in which a hydrogen from one of the methyl groups is replaced by a hydroxy group. It is registered for use in apple and pear orchards as a Lepidopteran pheromone/sex attractant, used to disrupt the mating behaviour of certain moths whose larvae destroy crops. It has a role as a cosmetic, a pheromone, an insect attractant, a pesticide and a plant metabolite. It is a primary alcohol, a fatty alcohol and a member of Lauryl alcohols. It derives from a hydride of a dodecane.

Computed Properties    HelpNew Window
Property Name    Property Value    Reference
Molecular Weight of Lauryl alcohol:    186.33 g/mol    Computed by PubChem 2.1 (PubChem release 2019.06.18)
XLogP3    5.1    Computed by XLogP3 3.0 (PubChem release 2019.06.18)
Hydrogen Bond Donor Count of Lauryl alcohol:    1    Computed by Cactvs 3.4.6.11 (PubChem release 2019.06.18)
Hydrogen Bond Acceptor Count of Lauryl alcohol:    1    Computed by Cactvs 3.4.6.11 (PubChem release 2019.06.18)
Rotatable Bond Count of Lauryl alcohol:    10    Computed by Cactvs 3.4.6.11 (PubChem release 2019.06.18)
Exact Mass of Lauryl alcohol:    186.198365 g/mol    Computed by PubChem 2.1 (PubChem release 2019.06.18)
Monoisotopic Mass of Lauryl alcohol:    186.198365 g/mol    Computed by PubChem 2.1 (PubChem release 2019.06.18)
Topological Polar Surface Area of Lauryl alcohol:    20.2 Ų    Computed by Cactvs 3.4.6.11 (PubChem release 2019.06.18)
Heavy Atom Count of Lauryl alcohol:    13    Computed by PubChem
Formal Charge of Lauryl alcohol:    0    Computed by PubChem
Complexity of Lauryl alcohol:    81.2    Computed by Cactvs 3.4.6.11 (PubChem release 2019.06.18)
Isotope Atom Count of Lauryl alcohol:    0    Computed by PubChem
Defined Atom Stereocenter Count of Lauryl alcohol:    0    Computed by PubChem
Undefined Atom Stereocenter Count of Lauryl alcohol:    0    Computed by PubChem
Defined Bond Stereocenter Count of Lauryl alcohol:    0    Computed by PubChem
Undefined Bond Stereocenter Count of Lauryl alcohol:    0    Computed by PubChem
Covalently-Bonded Unit Count of Lauryl alcohol:    1    Computed by PubChem
Compound Is Canonicalized of Lauryl alcohol:    Yes

LAURYL ALCOHOL
LAURYL ALCOHOL is classified as :
Emollient
Emulsifying
Emulsion stabilising
Viscosity controlling
CAS Number    112-53-8
EINECS/ELINCS No:    203-982-0
COSING REF No:    77060
Chem/IUPAC Name:    Dodecan-1-ol

Ethoxylated alcohol formulas such as Lauryl Alcohol are classified as surfactants, which means they reduce surface tension in a liquid, or between a liquid and a solid. As with all types of ethoxylated alcohol, Lauryl Alcohol Ethoxylate is a nonionic compound — it has no electrical charge on the hydrophilic end and generally takes the form of a thick liquid that is often sticky to the touch. The ethoxylation process also tends to increase the water solubility of the material. Products that typically contain Lauryl Alcohol Ethoxylate include cosmetics, laundry detergents, surface cleaners and personal care products, to name a few.
 effective Lauryl Alcohol Ethoxylate product in 2-mole and 3-mole liquid formulations. The 2-mole formula features a hydroxyl value of 198-206 mg KOH/g, a maximum moisture content of .10 percent and a pH ranging from 6.0 to 7.5. The 3-MOL version includes the same pH levels and moisture content, but it has a hydroxyl value of 171-180 mg KOH/g.
has been serving the oleochemical needs of companies throughout North America for more than 70 years. Our close partnerships with many of the top oleochemical manufactures ensures you will receive an effective ethoxylated alcohol product at a competitive price.Lauryl Alcohol Ethoxylate should be used with extreme caution. It is harmful if ingested and also poses a hazard to aquatic life. It is also likely to cause irritation when coming in contact with the eyes or skin. The product should be stored in a closed container in an area with a temperature ranging from 30-40° C.

USES & APPLICATIONS of Lauryl alcohol: 
Ethoxylated alcohol has multiple industrial uses and applications including:CASE: Use Lauryl Alcohol Ethoxylate as a wetting agent to reduce the surface tension in liquids, and as an emulsifier in paints and coatings to promote dispersion.Personal Care: Lauryl Alcohol Ethoxylate works extremely well as a foaming agent in personal care products such as shampoos and bath gels.Soaps and Detergents: Lauryl Alcohol serves as a reliable wetting agent in a wide range of industrial and household cleaning products including detergents, laundry pre-spotters and hard surface cleaners.Surfactants and Esters: You can use Lauryl Alcohol as a surfactant intermediate — it can also be sulfonated to make SLES (Sodium Lauryl Ether Sulfate), an anionic surfactant and detergent used in the manufacturing of many personal care products.Textiles: Use Lauryl Alcohol Ethoxylate as a wetting agent in textile and leather processing applications to reduce surface tension.

GRADES AND FORMS AVAILABLE  of Lauryl alcohol:
Liquid, Moles 2, 3, 4, 5, 7

PACKAGING of Lauryl alcohol:
Drums, Isotanks

INCI NAME of Lauryl alcohol:
The INCI Name varies by grade. The 2 Mole INCI is Laureth 2. The 3 Mole INCI is Laureth 3 and so on

CHEMICAL PROPERTIES of LAURYL ALCOHOL

FORMULA of LAURYL ALCOHOL : C12H26O
Molar Mass of LAURYL ALCOHOL:186.3342
HAZARD of LAURYL ALCOHOL: 0 Non-Regulated Material
APPEARANCE of LAURYL ALCOHOL: Colorless leaflets
COLOR of LAURYL ALCOHOL: TRANSPARENT
ODOR of LAURYL ALCOHOL: A LIGHT CHARACTERISTIC COCK.
DANGER of LAURYL ALCOHOL: THERAPEUTIC TEMPERATURE WILL CAUSE A LIGHT IRRITATION. WRITE WITH TEMPERATURE BOTH WATER PRIORITY.
ACID VALUE of LAURYL ALCOHOL: 0.1 mgKOH/gm Max.
FLAME POINT  of LAURYL ALCOHOL(° C): 119
BOILING POINT of LAURYL ALCOHOL (° C): 258
MELTING POINT of LAURYL ALCOHOL (° C): 24 - 25
DENSITY of LAURYL ALCOHOL 0,83 GR / CM3
Specific Gravity of LAURYL ALCOHOL: 0.82 (Water = 1)
SOLUBILITY of LAURYL ALCOHOL does not dissolve in the water.
SAPONIFICATION VALUE of LAURYL ALCOHOL: 0.5 mgKOH/gm Max.
IODINE VALUE of LAURYL ALCOHOL: 0.1 Max.
MOISTURE CONTENTv: 0.1% Max.
COLOR of LAURYL ALCOHOL: 10 Max. (APHA)
SOLIDIFICATION POINT of LAURYL ALCOHOL: 22 - 24°C
HYDROXYL VALUE of LAURYL ALCOHOL:298 - 302 mgKOH/gm
HYDROCARBONS of LAURYL ALCOHOL:0.5% Max.

GENERAL IMFORMATION ABOUT LAURYL ALCOHOL

Dodecanol also called as Lauryl alcohol or 1-dodecanol is classified as a fatty alcohol. It is a colorless, tasteless solid with a floral smell. It is manufactured by hydrogenation of palm kernel or coconut oil fatty acids. The major use of dodecanol is as a chemical intermediate for the manufacture of dodecyl sulfate and dodecyl ethoxylate. Additionally, it is used as a vital raw material in the manufacture of surfactants. It is also used in the manufacture of pharmaceuticals, lubricating oils, flavoring agents and as an emollient among other.

Dodecanol is used primarily as a chemical intermediate for the production of n-Dodecyl sulfate salts, and in the manufacture of n-Dodecyl ethoxylates. It also finds use in synthetic detergents, lube additives, pharmaceuticals,cosmetics, rubber, textiles, perfumes, and as a flavouring agent.Dodecanol is used to make surfactants, lubricating oils, pharmaceuticals, in the formation of monolithic polymers and as a flavor enhancing food additive. In cosmetics, dodecanol is used as an emollient. It is also the precursor to dodecanal, an important fragrance.

APPLICATION of LAURYL ALCOHOL

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)

STABILITY AND STORAGE of LAURYL ALCOHOL

KEEP IN TIGHTLY CLOSED CONTAINER IN A COOL AND DRY PLACE, PROTECTED FROM LIGHT. WHEN STORED FOR MORE THAN 24 MONTHS, QUALITY SHOULD BE CHECKED BEFORE USE.

DISPOSAL of LAURYL ALCOHOL

Whatever cannot be saved for recovery or recycling should be managed in an appropriate and approved waste disposal facility. Processing, use or contamination of this product may change the waste management options. State and local disposal regulations may differ from federal disposal regulations. Dispose of container and unused contents in accordance with federal, state and local requirements.

Molecular Weight of Lauryl alcohol:    186.33 g/mol    Computed by PubChem 2.1 (PubChem release 2019.06.18)
XLogP3    5.1    Computed by XLogP3 3.0 (PubChem release 2019.06.18)
Hydrogen Bond Donor Count of Lauryl alcohol:    1    Computed by Cactvs 3.4.6.11 (PubChem release 2019.06.18)
Hydrogen Bond Acceptor Count of Lauryl alcohol:    1    Computed by Cactvs 3.4.6.11 (PubChem release 2019.06.18)
Rotatable Bond Count of Lauryl alcohol:    10    Computed by Cactvs 3.4.6.11 (PubChem release 2019.06.18)
Exact Mass of Lauryl alcohol:    186.198365 g/mol    Computed by PubChem 2.1 (PubChem release 2019.06.18)
Monoisotopic Mass of Lauryl alcohol:    186.198365 g/mol    Computed by PubChem 2.1 (PubChem release 2019.06.18)
Topological Polar Surface Area of Lauryl alcohol:    20.2 Ų    Computed by Cactvs 3.4.6.11 (PubChem release 2019.06.18)
Heavy Atom Count of Lauryl alcohol:    13    Computed by PubChem
Formal Charge of Lauryl alcohol:    0    Computed by PubChem
Complexity of Lauryl alcohol:    81.2    Computed by Cactvs 3.4.6.11 (PubChem release 2019.06.18)
Isotope Atom Count of Lauryl alcohol:    0    Computed by PubChem
Defined Atom Stereocenter Count of Lauryl alcohol:    0    Computed by PubChem
Undefined Atom Stereocenter Count of Lauryl alcohol:    0    Computed by PubChem
Defined Bond Stereocenter Count of Lauryl alcohol:    0    Computed by PubChem
Undefined Bond Stereocenter Count of Lauryl alcohol:    0    Computed by PubChem
Covalently-Bonded Unit Count of Lauryl alcohol:    1    Computed by PubChem
Compound Is Canonicalized of Lauryl alcohol:    Yes