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Chemical compound
2-Ethylhexanol (abbreviated 2-EH) is an organic compound with the chemical formula CH3CH2CH2CH2CH(CH2CH3)CH2OH. It is a branched, eight-carbon chiral
2-Ethylhexanol
Chemical compound
to 2-ethylhexanoic acid and 2-ethylhexanol, both used as precursors to plasticizers. It was studied in the detergent industry since the 1930s. 2-Ethylhexanal
2-Ethylhexanal
Organic compound used as a plasticizer
branched-chain 2-ethylhexanol. This colorless viscous liquid is soluble in oil, but not in water. DEHP is produced commercially by the reaction of excess 2-ethylhexanol
Bis(2-ethylhexyl)_phthalate
Chemical compound
sun. It is an ester formed by the condensation of salicylic acid with 2-ethylhexanol. It is a colorless oily liquid with a floral odor. The salicylate portion
2-Ethylhexyl_salicylate
Chemical compound
C6H4(CO2C8H17)2. It is a diester of terephthalic acid and the branched-chain 2-ethylhexanol, which is often generically referred to as octyl. This colorless viscous
Bis(2-ethylhexyl) terephthalate
Bis(2-ethylhexyl)_terephthalate
Chemical compound
(C8H17O)2PO2H. The colorless liquid is a diester of phosphoric acid and 2-ethylhexanol. It is used in the solvent extraction of uranium, vanadium and the rare-earth
Di(2-ethylhexyl)phosphoric acid
Di(2-ethylhexyl)phosphoric_acid
Chemical compound
Bis(2-ethylhexyl) adipate or DEHA is an organic compound with the formula (CH2CH2CO2C8H17)2. It is the diester of 2-ethylhexanol and adipic acid. It is
Bis(2-ethylhexyl)_adipate
Water-insoluble oily ingredient used in some sunscreens
ester formed by the condensation of 2-ethylhexanol with dimethylaminobenzoic acid. Other names for padimate O include 2-ethylhexyl 4-dimethylaminobenzoate
Padimate_O
8-Carbon branched fatty acid
Nickel(II) ethylhexanoate (CAS# 4454-16-4) 2-Ethylhexanoic acid is banned in the EU for use in cosmetics. 2-Ethylhexanol "2-ethylhexanoic acid - Compound Summary"
2-Ethylhexanoic_acid
Chemical compound
can be described as the double ester of maleic acid with the alcohol 2-ethylhexanol. It is commonly called dioctyl maleate (DOM), reflecting the older usage
Bis(2-ethylhexyl)_maleate
Chemical used to separate emulsions
such as xylene, heavy aromatic naphtha (HAN), Isopropanol, methanol, 2-Ethylhexanol or diesel. Demulsifiers are manufactured by chemical manufacturers including:
Demulsifier
Chemical compound
musty. Racemic 2-ethylhexyl acrylate can be prepared with a high yield by esterification of acrylic acid with racemic 2-ethylhexanol in the presence
2-Ethylhexyl_acrylate
Chemical compound
also be prepared by a production route that is similar to that for 2-ethylhexanol: Such compounds enjoy many applications, including as raw materials
2-Propylheptanol
Chemical compound (CH2CH2CO2C8H17)2
with the formula (CH2CH2CO2C8H17)2. It is a colorless oily liquid . As well as related diesters derived from 2-ethylhexanol, decanol, isodecanol, etc., it
Dioctyl_adipate
Simplest secondary alcohol
Isopropyl alcohol (IUPAC name propan-2-ol and also called isopropanol or 2-propanol, commonly abbreviated as IPA) is a colorless, flammable, organic compound
Isopropyl_alcohol
Group of isomers (C8H17OH)
chain of carbons. Other commercially important octanols are 2-octanol and 2-ethylhexanol. Some octanols occur naturally in the form of esters in some
Octanol
Type of chemical
2-ethylhexyl nitrate (CAS n°: 27247-96-7) which starts to decompose at 130 °C. 2-ethylhexyl nitrate is the result of the reaction of 2-ethylhexanol and
Cetane_improver
Chemical compound
di(2-ethylhexyl) sebacate, commonly abbreviated as DOS, DEHS, and BEHS) is an organic compound which is the diester of sebacic acid and 2-ethylhexanol.
Dioctyl_sebacate
Group of chemical compounds
that are sold in commerce include the following: 2-Methyl-2-butanol (2M2B) n-Butanol 2-Ethylhexanol 2-Propylheptanol Isononyl alcohol Isodecyl alcohol
Oxo_alcohol
Chemical compound
also known as octyl palmitate, is the fatty acid ester derived from 2-ethylhexanol and palmitic acid. It is frequently utilized in cosmetic formulations
Ethylhexyl_palmitate
Chemical reaction
original 1899 publication concerned the conversion of n-butanol to 2-ethylhexanol. 2-ethylhexanol is however more easily prepared by alternative methods (from
Guerbet_reaction
Chemical compound
It is the fluoroacetate (FCH2CO2−) ester of 2-ethylhexanol, in other words, the 2-ethylhexyl (−CH2CH(CH2CH3)CH2CH2CH2CH3) ester of fluoroacetic
2-Ethylhexyl_fluoroacetate
Study of developmental anomalies
di-(2-ethylhexyl)-phthalate is hydrolyzed into 2-ethylhexanol. It's hypothesized that the metabolic byproduct of 2-ethylhexanol, ethylhexanoic acid, is the primary
Teratology
UV-B protectant used in sunscreens
and lip balms. It is an ester formed from methoxycinnamic acid and 2-ethylhexanol. It is a liquid that is insoluble in water. It is primarily used in
Octyl_methoxycinnamate
Chemical compound
2-Methylheptane is a branched-chain alkane and an isomer of octane. It is an heptane molecule with a methyl group attached to its second atom. It is a
2-Methylheptane
Chemical compound
(sometimes represented as t-BuOH). Its isomers are 1-butanol, isobutanol, and 2-butanol. tert-Butyl alcohol is a colorless solid, which melts near room temperature
Tert-Butyl_alcohol
Chemical compound
where its presence helps reduce viscosity and lower freezing points. 2-Ethylhexanol Lide, David R. (1998), Handbook of Chemistry and Physics (87 ed.), Boca
2-Ethyl-1-butanol
Chemical compound
(BFR). TBPH is the diester of tetrabromophthalic acid and (racemic) 2-ethylhexanol. It has two stereocenters, located at the carbon atoms carrying the
Bis(2-ethylhexyl)tetrabromophthalate
Bis(2-ethylhexyl)tetrabromophthalate
Chemical compound
Dictionary. National Cancer Institute. 2 February 2011. Archived from the original on 2 May 2019. Retrieved 2 May 2019. E. Bertani; A. Chiappa; R. Biffi;
Glycerol
Carbocyclic sugar
Cellular and Medical Aspects. Academic Press. p. 348. ISBN 978-0-08-047207-2. Goel, Meenakshi; Azev, Viatcheslav N; d‘Alarcao, Marc (April 2009). "The
Inositol
Secondary alcohol CH3CH(OH)CH2CH3
Butan-2-ol, or sec-butanol, is an organic compound with formula CH3CH(OH)CH2CH3. Its structural isomers are 1-butanol, isobutanol, and tert-butanol. 2-Butanol
2-Butanol
Organic compound
feedstock. As of 2024, world production of ethanol fuel was 120 gigaliters (3.2×1010 U.S. gallons), coming mostly from the U.S. (51%) and Brazil (30%). The
Ethanol
Salt or ester of acrylic acid
catalysts (cation exchanger). The reaction of higher alcohols (n-butanol, 2-ethylhexanol) is catalysed with sulfuric acid in homogeneous phase. Acrylates of
Acrylate
Chemical compound
It has the IUPAC name of 2-(2-ethylhexoxymethyl)oxirane. It also finds use in other polymer based applications. 2-Ethylhexanol and epichlorohydrin are
2-Ethylhexyl_glycidyl_ether
Class of organic compounds
which is 2-propanol (R = R' = CH3). For the tertiary alcohols, the general form is RR'R"COH. The simplest example is tert-butanol (2-methylpropan-2-ol), for
Alcohol_(chemistry)
Natural sweetener
Xylitol is an organic compound with the formula HOCH(CH(OH)CH2OH)2. Two other isomeric sugar alcohols exist. It is a colorless or white crystalline solid
Xylitol
Organic compound containing the functional group R–CH=O
are prepared by hydroformylation. It is the principal precursor to 2-ethylhexanol, which is used as a plasticizer. Acetaldehyde once was a dominating
Aldehyde
Laxatives/stool softeners
described as the twofold carboxylate ester of sulfosuccinic acid with 2-ethylhexanol. The compound is a white, wax-like, plastic solid, with an odor suggestive
Docusate
Index of chemical compounds with the same molecular formula
23 g/mol) may refer to: Di-tert-butyl ether Dibutyl ether 2-Ethylhexanol Octanols 1-Octanol 2-Octanol 3-Octanol This set index page lists chemical structure
C8H18O
Set of reactions to attach substituents to an aromatic ring
aluminium chloride is replaced by graphite in an alkylation of p-xylene with 2-bromobutane. This variation will not work with primary halides from which
Friedel–Crafts_reaction
Sugar alcohol that is used as a sweetener
using enzymes and fermentation. Its formula is C 4H 10O 4, or HO(CH2)(CHOH)2(CH2)OH. Erythritol is 60–70% as sweet as table sugar. However, erythritol
Erythritol
Chemical compound (C4H9OH)
CH3(CH2)3OH and a linear structure. Isomers of 1-butanol are isobutanol, butan-2-ol and tert-butanol. The unmodified term butanol usually refers to the straight
1-Butanol
Organic compound ethane-1,2-diol
(IUPAC name: ethane-1,2-diol) is an organic compound with the formula (CH2OH)2. It is the simplest vicinal diol. It is mainly used for two purposes: as a
Ethylene_glycol
Organic compounds
is obtained by the fermentation of glucose and sucrose. Ethylene glycol (2-carbon) Glycerol (3-carbon) Erythritol (4-carbon) Threitol (4-carbon) Arabitol
Sugar_alcohol
Chemical compound
2-dehydrogenase. Sorbitol is an isomer of mannitol, another sugar alcohol; the two differ only in the orientation of the hydroxyl group on carbon 2.
Sorbitol
Chemical compound
tert-Amyl alcohol (TAA) or 2-methylbutan-2-ol (2M2B), is a branched pentanol. Historically, TAA has been used as an anesthetic and more recently as a
Tert-Amyl_alcohol
Chemical reaction
notably of pentaerythritol, trimethylolpropane, the plasticizer precursor 2-ethylhexanol, and the drug Lipitor (atorvastatin, calcium salt). For many of the
Aldol_reaction
Chemical compound
3-Methylhexane 2-Methylheptane Related compounds Valnoctamide 2-Ethylhexanol Valpromide 2-Ethylhexanoic acid Propylheptyl alcohol Except where otherwise
3-Methylheptane
Chemical compound
the production 2-ethylhexyl sulfate, a wetting agent used in the mercerisation of cotton, by combining sulfamic acid with 2-ethylhexanol. Sulfamic acid
Sulfamic_acid
Chemical compound
that way speciality acrylates are made accessible, e.g. 2-ethylhexyl acrylate (from 2-ethylhexanol) used for pressure-sensitive adhesives, cyclohexyl acrylate
Ethyl_acrylate
Organic chemical compound
CH3CHO → CH3CH(O−)PCl+3 CH3CH(O−)PCl+3 + 2 CH3CO2H → CH3CH(Cl)PO(OH)2 + 2 CH3COCl CH3CH(Cl)PO(OH)2 → CH2=CHPO(OH)2 + HCl In the liver, the enzyme alcohol
Acetaldehyde
Type of chemical reaction
Exxon, converts propene and syngas to 2-ethylhexanol via hydroformylation to butyraldehyde, aldol condensation to 2-ethylhexanal and finally hydrogenation
Aldol_condensation
Chemical compound
alcohol; the two differ only in the orientation of the hydroxyl group on carbon 2. While similar, the two sugar alcohols have very different sources in nature
Mannitol
Chemical compound
2-Methyl-2-pentanol (IUPAC name: 2-methylpentan-2-ol) is an organic chemical compound. It can be added to a gas chromatograph to help distinguish between
2-Methyl-2-pentanol
Chemical compound
2-Nonanol is a simple alcohol. It has the odor of cucumber, and has been identified in oysters. It is used by several insects as pheromones. It is commercially
2-Nonanol
Sedative-hypnotic drug
structure is considerably simpler. The systematic name is usually given as ethyl 2-chlorovinyl ethynyl carbinol or 1-chloro-3-ethylpent-1-en-4-yn-3-ol. Its empirical
Ethchlorvynol
Chemical compound
2-Fluoroethanol is the organic compound with the formula CH2FCH2OH. This colorless liquid is one of the simplest stable fluorinated alcohols. It was once
2-Fluoroethanol
Alcohols used as antiseptics, disinfectants or antidotes
(69th ed.). British Medical Association. 2015. pp. 42, 838. ISBN 978-0-85711-156-2. Stuart MC, Kouimtzi M, Hill SR, eds. (2009). WHO Model Formulary 2008. World
Alcohols_(medicine)
Coordination complexes of transition metals and metal ions with carbon monoxide ligands
→ CH3CH2CH2CHO Butyraldehyde is converted on an industrial scale to 2-ethylhexanol, a precursor to PVC plasticizers, by aldol condensation, followed by
Metal_carbonyl
Chemical compound
1-Hexatetracontanol 1-Heptatetracontanol 1-Octatetracontanol 1-Nonatetracontanol 2-Ethylhexanol Allyl alcohol Anisyl alcohol Benzyl alcohol Cinnamyl alcohol Crotyl
Arachidyl_alcohol
Chemical compound
1-Hexatetracontanol 1-Heptatetracontanol 1-Octatetracontanol 1-Nonatetracontanol 2-Ethylhexanol Allyl alcohol Anisyl alcohol Benzyl alcohol Cinnamyl alcohol Crotyl
Isoamyl_alcohol
Chemical compound
1-Hexatetracontanol 1-Heptatetracontanol 1-Octatetracontanol 1-Nonatetracontanol 2-Ethylhexanol Allyl alcohol Anisyl alcohol Benzyl alcohol Cinnamyl alcohol Crotyl
1-Dotriacontanol
Chemical compound
1-Hexatetracontanol 1-Heptatetracontanol 1-Octatetracontanol 1-Nonatetracontanol 2-Ethylhexanol Allyl alcohol Anisyl alcohol Benzyl alcohol Cinnamyl alcohol Crotyl
1-Octen-3-ol
Sugar alcohol used as a sweetener
capsules, as an emollient, and as a humectant. Maltitol provides between 2 and 3 kilocalories per gram [kcal/g] (8–10 kJ/g). Maltitol is largely unaffected
Maltitol
Chemical compound
1-Hexatetracontanol 1-Heptatetracontanol 1-Octatetracontanol 1-Nonatetracontanol 2-Ethylhexanol Allyl alcohol Anisyl alcohol Benzyl alcohol Cinnamyl alcohol Crotyl
1-Pentanol
29-carbon primary fatty alcohol
1-Hexatetracontanol 1-Heptatetracontanol 1-Octatetracontanol 1-Nonatetracontanol 2-Ethylhexanol Allyl alcohol Anisyl alcohol Benzyl alcohol Cinnamyl alcohol Crotyl
1-Nonacosanol
Chemical compound (CH3)2CHCH2OH
Isobutanol (IUPAC nomenclature: 2-methylpropan-1-ol) is an organic compound with the formula (CH3)2CHCH2OH (sometimes represented as i-BuOH). This colorless
Isobutanol
Chemical compound
3-dimethylbutan-2-ol and as pine alcohol) is one of the isomeric hexanols and a secondary alcohol. Pinacolyl alcohol appears on the List of Schedule 2 substances
Pinacolyl_alcohol
Aromatic alcohol
reproductive effects. Benzyl alcohol has low acute toxicity with an LD50 of 1.2 g/kg in rats. It oxidizes rapidly in healthy individuals to benzoic acid,
Benzyl_alcohol
Chemical compound
2-Methyl-1-butanol (IUPAC name, also called active amyl alcohol) is an organic compound with the formula CH3CH2CH(CH3)CH2OH. It is one of several isomers
2-Methyl-1-butanol
Chemical compound
2-Pentanol (IUPAC name: pentan-2-ol; also called sec-amyl alcohol) is an organic chemical compound. It is used as a solvent and an intermediate in the
2-Pentanol
Chemical reaction which exchanges the R groups of an alcohol and ester
transesterification, giving access to vinyl ethers: ROH + AcOCH=CH 2 ⟶ ROCH=CH 2 + AcOH The reaction can be effected with high enantioselectivity when
Transesterification
Chemical compound
1-Hexatetracontanol 1-Heptatetracontanol 1-Octatetracontanol 1-Nonatetracontanol 2-Ethylhexanol Allyl alcohol Anisyl alcohol Benzyl alcohol Cinnamyl alcohol Crotyl
1-Tetracosanol
Chemical compound
oxidation of cyclohexane in air, typically using cobalt catalysts: 2 C6H12 + O2 → 2 C6H11OH This process coforms cyclohexanone, and this mixture ("KA oil"
Cyclohexanol
Organic reduction of any carbonyl group by a reducing agent
lithium aluminium hydride is: 2 RCO2R' + LiAlH4 → LiAl(OCH2R)2(OR') LiAl(OCH2R)2(OR') + 4 H2O → LiAl(OH)4 + 2 HOCH2R + 2 HOR' Sodium borohydride can, under
Carbonyl_reduction
Chemical compound
2-Hexanol (hexan-2-ol) is a six-carbon alcohol in which the hydroxy group (OH) is located on the second carbon atom. Its chemical formula is C6H14O or
2-Hexanol
CH3OH; simplest possible alcohol
areas, especially polymers. The conversion entails oxidation: 2 CH3OH + O2 → 2 CH2O + 2 H2O Acetic acid can be produced from methanol. Methanol and isobutene
Methanol
Type of chemical reaction
1-Hexatetracontanol 1-Heptatetracontanol 1-Octatetracontanol 1-Nonatetracontanol 2-Ethylhexanol Allyl alcohol Anisyl alcohol Benzyl alcohol Cinnamyl alcohol Crotyl
Fischer–Speier_esterification
Method for preparing ethers
Development. 9 (2): 206–211. doi:10.1021/op050001h. Tanabe, Masato; Peters, Richard H. (1981). "(R,S)-Mevalonolactone-2-13C (2H-Pyran-2-one-13C,
Williamson_ether_synthesis
Chemical compound
1-Hexatetracontanol 1-Heptatetracontanol 1-Octatetracontanol 1-Nonatetracontanol 2-Ethylhexanol Allyl alcohol Anisyl alcohol Benzyl alcohol Cinnamyl alcohol Crotyl
1-Tridecanol
Chemical compound
1-Hexatetracontanol 1-Heptatetracontanol 1-Octatetracontanol 1-Nonatetracontanol 2-Ethylhexanol Allyl alcohol Anisyl alcohol Benzyl alcohol Cinnamyl alcohol Crotyl
Fucitol
Class of chemical compounds
Weinheim: Wiley-VCH. doi:10.1002/14356007.a10_277.pub2. ISBN 978-3-527-30673-2. IUPAC, Compendium of Chemical Terminology, 5th ed. (the "Gold Book") (2025)
Fatty_alcohol
Chemical compound
ISBN 978-3-527-30673-2. Schwarzenbach RP, Gschwend PM, Imboden DM (2003). Environmental organic chemistry. John Wiley. ISBN 0-471-35053-2. McCarley KD, Bunge
1-Octanol
Primary alcohol compound (CH3CH2CH2OH)
represented as PrOH or n-PrOH. It is a colourless liquid and an isomer of 2-propanol. 1-Propanol is used as a solvent in the pharmaceutical industry,
1-Propanol
Chemical compound
amyl alcohol. It is found naturally and has a role as an insect pheromone. 2-Pentanol Lide, David R. (1998), Handbook of Chemistry and Physics (87 ed.)
3-Pentanol
Chemical compound
Phenethyl alcohol, or 2-phenylethanol, is an organic compound with the chemical formula C8H10O or C6H5(CH2)2OH. It is a colourless liquid with a pleasant
Phenethyl_alcohol
Isoamyl alcohol 2-Methyl-1-butanol Neopentyl alcohol 2-Pentanol 3-Methyl-2-butanol 3-Pentanol tert-Amyl alcohol 1-Hexanol 2-Hexanol 3-Hexanol 2-Methyl-1-pentanol
List_of_alkanols
Alcohol in which the hydroxy group is bonded to a primary carbon atom
1-Hexatetracontanol 1-Heptatetracontanol 1-Octatetracontanol 1-Nonatetracontanol 2-Ethylhexanol Allyl alcohol Anisyl alcohol Benzyl alcohol Cinnamyl alcohol Crotyl
Primary_alcohol
Chemical compound
2-Methyl-2-propyl-1,3-propanediol (MPP) is a simple alkyl diol which has sedative, anticonvulsant and muscle relaxant effects. It is both a synthetic precursor
2-Methyl-2-propyl-1,3-propanediol
2-Methyl-2-propyl-1,3-propanediol
Chemical compound
pronunciation and meaning of cetacean taxonomic names" (PDF). Aquatic Mammals. 27 (2): 185. Archived from the original (PDF) on 2016-03-27. Retrieved 2020-04-26
Cetyl_alcohol
Chemical compound
behavior modifying activity". Comparative Biochemistry and Physiology C. 60 (2): 175–185. doi:10.1016/0306-4492(78)90091-6. PMID 28889. Gil C, Gómez-Cordovés
Tryptophol
Chemical compound
3-Ethylpentane 2-Methylhexane 2-Methylheptane 3-Methylheptane Related compounds 2-Ethyl-1-butanol Valnoctamide 2-Ethylhexanol Valpromide 2-Ethylhexanoic
3-Methylhexane
Chemical compound
mono(1-ethyl-1-methyl-2-propynyl) ester) [131-67-9] Anansiol (1-ethyl-1-methylprop-2-ynyl carbamate) [302-66-9] Bason ( 2-Bromoethynyl-2-butanol) [2028-52-6]
Methylpentynol
Chemical reaction
aldehyde, which is transformed via an aldehyde hydrate (gem-diol, R-CH(OH)2) by reaction with water. Thus, the oxidation of a primary alcohol at the aldehyde
Alcohol_oxidation
Chemical compound
1-Hexatetracontanol 1-Heptatetracontanol 1-Octatetracontanol 1-Nonatetracontanol 2-Ethylhexanol Allyl alcohol Anisyl alcohol Benzyl alcohol Cinnamyl alcohol Crotyl
Mannosulfan
Mixture of sugar alcohols
1-Hexatetracontanol 1-Heptatetracontanol 1-Octatetracontanol 1-Nonatetracontanol 2-Ethylhexanol Allyl alcohol Anisyl alcohol Benzyl alcohol Cinnamyl alcohol Crotyl
Hydrogenated starch hydrolysates
Hydrogenated_starch_hydrolysates
Chemical compound
in a rat model of neuropathic pain". British Journal of Pharmacology. 146 (2): 198–208. doi:10.1038/sj.bjp.0706310. PMC 1576263. PMID 15997234. RH Belmaker;
Valnoctamide
Chemical compound
promote tooth decay and is considered to be tooth-friendly. Its energy value is 2 kcal per gram, half that of sugars. It is less sweet than sugar, but can be
Isomalt
Chemical compound
2-Heptanol is a chemical compound which is an isomer of heptanol. It is a secondary alcohol with the hydroxyl on the second carbon of the straight seven-carbon
2-Heptanol
Chemical compound
1-Hexatetracontanol 1-Heptatetracontanol 1-Octatetracontanol 1-Nonatetracontanol 2-Ethylhexanol Allyl alcohol Anisyl alcohol Benzyl alcohol Cinnamyl alcohol Crotyl
Undecanol
travel, tourism, insurance
2 ETHYLHEXANOL
2 ETHYLHEXANOL
Surname or Lastname
English
English : variant of Hackett 2.
Surname or Lastname
English
English : variant of Goodall 2.
Surname or Lastname
North German variant of Laas 2.Jewish (Ashkenazic)
North German variant of Laas 2.Jewish (Ashkenazic) : unexplained.English : nickname from Middle English lesse, lasse ‘smaller’ (from Old English lǣssa ‘less’), perhaps also used in the sense ‘younger’.
Surname or Lastname
English
English : variant of Maul 2.
Surname or Lastname
English
English : patronymic from Lamb 2.
Surname or Lastname
English
English : patronymic from Lamb 2.
Surname or Lastname
English
English : variant of Land 2.
Surname or Lastname
English
English : variant of Hayden 2.
Surname or Lastname
Variant of Nicolai 2.English
Variant of Nicolai 2.English : variant of Nicholas.
Surname or Lastname
English
English : patronymic from Lakin 2.
Surname or Lastname
English
English : variant of Mixon 2.
Surname or Lastname
English
English : patronymic from Lamb 2.
Surname or Lastname
English
English : variant of Diamond 2.
Surname or Lastname
English
English : variant of Greenfield 2.
Girl/Female
Indian
Mixture of 2 Names
Surname or Lastname
English
English : variant of Glad 2.
Surname or Lastname
English
English : variant of Haddock 2.
Boy/Male
Shakespearean
King Henry IV, Part 1' Earl of March. Scroop.
Surname or Lastname
English
English : patronymic from Lamb 2.
Surname or Lastname
English
English : variant of Garrett 2.
2 ETHYLHEXANOL
2 ETHYLHEXANOL
2 ETHYLHEXANOL
2 ETHYLHEXANOL
2 ETHYLHEXANOL
2 ETHYLHEXANOL
2 ETHYLHEXANOL
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