1 phenylethylamine pka

1-Phenylethylamine | C8H11N | CID 7408 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety/hazards/toxicity information, supplier lists, and more 1-Phenylethylamine is the organic compound with the formula C 6 H 5 CH(NH 2)CH 3.Classified as a monoamine, this colorless liquid is often used in chiral resolutions.Like benzylamine, it is highly basic and forms stable ammonium salts and imines.. This compound may be prepared by the reductive amination of acetophenone.One major route for this chemical uses the Mignonac reaction, a one-pot. (S)-(-)-1-Phenylethylamine. Molecular Formula C 8 H 11 N; Average mass 121.180 Da; Monoisotopic mass 121.089149 Da; ChemSpider ID 6832 Synthesis and Structure Determination of a Novel Layered Aluminophosphate Material Templated with 1-Phenylethylamine: [AlPO4(OH)](NH3C2H4C6H5). Chemistry of Materials 2007, 19 (9) , 2261-2268. DOI: 10.1021/cm070106u

1-Phenylethylamine (α-methylbenzylamine) 1 is a simple, cheap, and easily accessible chiral amine, which has been widely applied in the preparation of enantiomerically pure compounds. Applications of 1-phenylethylamine 1 in asymmetric synthesis have been the subject of several reviews. 1,2 Enantiopure 1 is readily available by resolution of the racemate with tartaric acid by crystallization ( Figure 1 ). Phenethylamine | C8H11N | CID 1001 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety. CID 59898296 | C8H10N- | CID 59898296 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities.

pKa Chart conjugate acid conjugate base conjugate acid conjugate base s t r o n g e s t a c i d s w e a k e s t b a s e s hydrogen sulfide 1 2 (bicarbonate) hydrochloric acid -7 carbocations - 121.18 g/mol. Date s. Modify. 2021-04-10. Create. 2004-09-16. (1S)-1-phenylethanamine is the (S)-enantiomer of 1-phenylethanamine. It is a conjugate base of a (1S)-1-phenylethanaminium. It is an enantiomer of a (1R)-1-phenylethanamine Molecular Weight. 121.18 g/mol. Date s. Modify. 2021-04-17. Create. 2005-07-19. (1R)-1-phenylethanamine is the (R)-enantiomer of 1-phenylethanamine. It is a conjugate base of a (1R)-1-phenylethanaminium Upon exposure to air, it combines with carbon dioxide to form a solid carbonate salt. Phenethylamine is strongly basic, pK b = 4.17 (or pK a = 9.83), as measured using the HCl salt, and forms a stable crystalline hydrochloride salt with a melting point of 217 °C

1-Phenylethylamine, also known as a-aminoethylbenzene or a-methylbenzylamine, belongs to the class of organic compounds known as aralkylamines. These are alkylamines in which the alkyl group is substituted at one carbon atom by an aromatic hydrocarbyl group. 1-Phenylethylamine is a very strong basic compound (based on its pKa) Synonym: (S)-(-)-1-Phenylethylamine Linear Formula: C 6 H 5 CH(CH 3)NH 2. Molecular Weight: 121.18. CAS Number: 2627-86-

Shop a large selection of Aralkylamines products and learn more about (S)-(-)-1-Phenylethylamine, 99+%, produced by BASF AG, ACROS Organics. 50g; Glass bottle Sans autre précision, le terme « phényléthylamine » désigne généralement la 2-phényléthylamine. Il désigne même en fait la famille des phényléthylamines substituées (en), une classe de composés dont la structure dérive de celle de la 2-phényléthylamine qui peuvent être des alcaloïdes, des hormones, des neurotransmetteurs, des stimulants divers, des produits hallucinogènes.

Synonym: (R)-(+)-1-Phenylethylamine CAS Number 3886-69-9. Linear Formula C 6 H 5 CH(CH 3)NH 2. Molecular Weight 121.18 . Beilstein/REAXYS Number 2410916 . EC Number 223-423-4. MDL number MFCD00064405. PubChem Substance ID 24847222. NACRES NA.2 GC Analysis of 1-Phenylethylamine Enantiomers (N-Acetyl Derivatives) on Astec® CHIRALDEX® B-DM. From our library of Articles, Sigma-Aldrich presents GC Analysis of 1-Phenylethylamine Enantiomers (N-Acetyl Derivatives) on Astec® CHIRALDEX® B-DM Keywords: Chromatography, Flame ionization detector, Gas chromatography, Purificatio (S)-(-)-1-Phenylethylamine for the resolution of racemates for synthesis Synonym: (S)-(-)-1-Phenylethylamine, L-α-Methylbenzylamine CAS Number 2627-86-3. Linear Formula C 6 H 5 CH(CH 3)NH 2. Molecular Weight 121.18 . MDL number MFCD00064406. EC Index Number 220-098 These are alkylamines in which the alkyl group is substituted at one carbon atom by an aromatic hydrocarbyl group. N,N-Dimethylphenethylamine is a very strong basic compound (based on its pKa). Its aroma is described as sweet, fishy. It is mainly used in cereal, cheese, dairy products, fish, fruit and meat

1-Phenylethylamine C8H11N - PubChe

1-Phenylethylamine (α-methylbenzylamine) 1 is a simple, cheap, and easily accessible chiral amine, which has been widely applied in the preparation of enantiomerically pure compounds.Applications of 1-phenylethylamine 1 in asymmetric synthesis have been the subject of several reviews. 1,2 Enantiopure 1 is readily available by resolution of the racemate with tartaric acid by crystallization. Chemsrc provides L-1-Phenylethylamine(CAS#:2627-86-3) MSDS, density, melting point, boiling point, structure, formula, molecular weight etc. Articles of L-1-Phenylethylamine are included as well

1-Phenylethylamine - Wikipedi

Bulk and Prepack available | Aldrich-115568; (S)-(?)-1-Phenylethylamine; CAS No. 2627-86-3; Explore related products, MSDS, application guides, procedures and protocols at Sigma Aldrich - a one stop solution for all your research & industrial needs *Upon orders receipt, Hyderabad stocks will be dispatched on the same day & Chennai stocks will be dispatched in 3-6 working days. *Items available in Japan warehouse will be dispatched in 10-12 working days

(S)-(-)-1-Phenylethylamine C8H11N ChemSpide

  1. e for the resolution of racemates for synthesis. CAS 2627-86-3, chemical formula C₆H₅CH(CH₃)NH₂. - Find MSDS or SDS, a COA, data sheets and more information
  2. e 2-phenylethyla
  3. e(2627-86-3) information like chemical properties,Structure,melting point,boiling point,density,molecular formula,molecular weight, physical properties,toxicity information,customs codes. You can also browse global suppliers,vendor,prices,Price,manufacturers of L-1-Phenylethyla

Anomalous pKa Values of Some Substituted

  1. e for the resolution of racemates for synthesis: 100 mL: $149.85: 2021-03-22: Buy: TCI Chemical P0794 (R)-(+)-1-Phenylethyla
  2. e compounds play a crucial role in numerous chemical and biological processes. Many biomolecules are a
  3. e ((S)-(-)-1-phenylethyla

1-Phenylethylamine - an overview ScienceDirect Topic

Phenethylamine C8H11N - PubChe

In addition, a depolarizing stimulus caused the Ca ++-dependent release of radiolabelled, as well as endogenous, mTA and pTA from rat slices. The characteristics of mTA and pTA uptake and release are those that have been associated with a neurotransmitter function; however, it appears that the release of mTA and pTA can originate from a different neuronal compartment than DA release 1-Phenylethylamine, or 1-phenylethanamine 604 Back Forward Main Menu TOC Study Guide TOC Student OLC MHHE Websit Diastereomeric salt formation Louis Pasteur was able to isolate the stereoisomers of tartaric acid because they crystallize from solution as crystals with differing symmetry and shape. (S)-1-Phenylethylamine combines with a racemic mixture of tartaric acid to form diastereomeric salts ,which are seperated by crystallization. After seperation each of the diastereomers are treated with strong acid(Example: HCL) to regenerate the corresponding enantiomer of tartaric acid L'ibuprofène est un principe actif de la famille des anti-inflammatoires non stéroïdiens (AINS). Il est utilisé pour réduire la douleur (action..

CID 59898296 C8H10N- - PubChe

Finally, it was demonstrated that SA-B exhibited a protective effect on MI mainly by decreasing the concentration of cyclic adenosine monophosphate (cAMP) and Ca2+ and inhibiting protein kinase A (PKA). SA-B and propanolol exhibited similar metabolomic profiles, indicating that the two drugs might have a similar mechanism Molarity Calculator. * Our calculator is based on the following equation: Concentration ( start) x Volume ( start) = Concentration ( final) x Volume ( final) It is commonly abbreviated as: C 1 V 1 = C 2 V 2. Calculate. * Total Molecular Weight: g/mol. Tip: Chemical formula is case sensitive. C22H30N4O √ c22h30n40 ╳

b. React 2,3-pentadienedioic acid mixture with a chiral base such as (R)‑1‑phenylethylamine. Reaction will produce a mixture of diastereomeric salts. Separate diastereomers through crystallization. Treat salt with strong acid (e.g. HCl) to recover the pure enantiomer acid. c. React 1-phenylethanol mixture with 1,2-benzenedicarboxylic anhydride Lookchem Provide Cas No.87-69-4 Basic information: Properties,Safety Data,Sds and Other Datebase. We also Provide Trading Suppliers & Manufacture for 87-69-4 L(+)-Tartaric acid

(1S)-1-Phenylethanamine C8H11N - PubChe

(1R)-1-Phenylethanamine C8H11N - PubChe

  1. es on coordinated ligands. Several pathways for the a
  2. Abstract. This thesis reports diverse synthetic and mechanistic studies in six chapters, as summarized below. Chapter 1. Revised mechanism and improved methodology for the perkin condensation.1 The generally accepted mechanism for the well-known Perkin condensation is unviable for at least two reasons: (1) the normally employed base, acetate ion, is too weak to deprotonate acetic anhydride.
  3. e, phytosphingosine, L-isoleucyl-L-proline, 2',3'-Cyclic GMP, 1-phenylethyla
  4. In enzymology, a kinase is an enzyme that catalyzes the chemical reaction ATP + phosphotransferase. Other names in common use include pheochromocytoma tyrosine hydroxylase-associated kinase, STK4, and tyrosine 3-monooxygenase kinase phosphorylating. This enzyme participates in MAPK signaling pathway and non-small cell lung cancer
  5. e into a conglomerate upon salt formation with an achiral acid. Just how deter
  6. Co-facial porphyrins have been designed to construct porphyrin tweezers with versatile molecular recognition capabilities. In this study, we synthesized metalloporphyrin-peptoid conjugates (MPPCs) displaying two metalloporphyrins on a peptoid scaffold with either achiral unfolded (1) or helical (2 and 3) secondary structures. Host-guest complexation of MPPCs was realized with various.
  7. o acid L - tyrosine to L - 3 4 - dihydroxyphenylalanine kinase kinase abbreviated as MKK, MEK, or MAP2K and then MAPK1 2 below Ras is typically activated by growth hormones through receptor tyrosine kinases biochemistry, a dual - specificity kinase EC is a kinase that.

Phenethylamine - Wikipedi

Showing metabocard for 1-Phenylethylamine (HMDB0002017

pKa;9.90±0.10(25 oC. 物理性质: 苯乙胺是一种芳香胺,在室温时是无色液体。 应用: 苯乙胺为重要的医药和染料中间体,在医药上主要用于合成以下药物. 该品为药物降糖灵的中间体。也用于其他有机合成 acetic acid has a pka of 4.8 how many ml of 0.1M acetic acid and 0.1M sodium acetate are required to prepare 1L of 0.1M buffer with a PH of 5.8? solve . science {chemistry) 30ml of 0.1M of sodium hydroxide is added to 100Ml of 0.1M of acetic acid, then what is the pH of the buffer solution, where (Ka =1.85 ×10*-10 for acetic acid.

There is a linear correlation between enzymatic activity and the pKa of the phenolic leaving group for 16 paraoxon analogues. The beta value in the corresponding Bronsted plot is -0.8. No effect on either more » Vmax or Vmax/Km is observed when sucrose is used to increase the relative solvent viscosity by 3-fold 1-phenylethylamine was obtained in a yield of 4.3% of theory (100% selectivity). Each document, patent, patent application or patent publication cited by or referred to in this disclosure is incorporated by reference in its entirety, especially with respect to the specific material surrounding the citation of the reference in the text Total radioactivity added to the cells was 10 μCi/ml, resulting in specific radioactivities of 18 − 1 Ci/mol glucose. Cellular metabolism was stopped by the addition of 50 μl of 0.2 mol/l HCl, and the produced 14 CO 2 was captured by the addition of 100 μl 1-phenylethylamine A solution of 13 g (78.6 mmol) of 1-(4-Methoxy-phenyl)-propan-2-one and 8.3 g (78.6 mmol) of (R)-1-Phenylethylamine in 60 mL MeOH was hydrogenated in the presence of 1.7 g of Pt/C 5% at 10 atm. and 30 °C for 20 h. The mixture was filtered though a pad of diatomaceous earth and concentrated under reduced pressure to give compound III as an oil

1-phenylethylamine Sigma-Aldric

Identification of a novel class of selective Tpl2 kinase inhibitors: 4-Alkylamino-[1,7]naphthyridine-3-carbonitrile Lookchem Provide Cas No.65-85- Basic information: Properties,Safety Data,Sds and Other Datebase. We also Provide Trading Suppliers & Manufacture for 65-85- Benzoic acid

How many milliliters of 0.202 M KOH should be added to 500.0 mL of 0.0233 M tartaric acid (C4H6O6; FW 150.087) to adjust the pH to 2.75? Ka1 = 1.0 x 10-13 and Ka2 = 4.6 x10-5. For this one, the Ka1 seems sort of off. The pka would be 13 which doesn't make . chemistr Research papers, journal articles and scientific articles related to biocatalysis: Here you will find abstracts and references of the latest publications from journals in this sector 65. th. AR YE. Annual subscription: Rs. 1500 Price per copy: Rs. 29. May 12, 2020. Content. Index to Advertisers. Index to Products Advertise

(S)-(-)-1-Phenylethylamine, 99+%, produced by BASF AG

Thermodynamics of acid-base dissociation of several cathinones and 1‐phenylethylamine, studied by an accurate capillary electrophoresis method free from the Joule heating impact Author: Nowak, Paweł Mateusz; Woźniakiewicz, Michał; Mitoraj, Mariusz; Sagan, Filip; Kościelniak, Pawe Using histidines (pKa ∼6.1) as cationic residues has been reported to result in the pH-dependent activity of anticancer peptides with enhanced selectivity against tumor environments in vivo which are significantly more acidic than normal tissues To confirm this, R and S bromopropionic acid were condensed with a chiral amine ((S)-(-)-1-phenylethylamine) under these conditions. No evidence for racemization was observed in the nuclear magnetic resonance spectrum of the final products (see Figure S2 )

esters.18 This analogy is supported by the observation compared to other bases could be ascribed to its nucleo- of the inefficiency of MTBD for the catalysis of amino- philicity and to a bifunctional nucleophilic mechanism. lysis despite a similar basicity than TBD (pKa values of conjugate acid are 25.7 and 26.2, respectively) Yeast strains were trans- Chemicals formed using the lithium acetate method (Gietz and Schiestl 2007), and transformants were selected on yeast nitrogen base Acetophenone (ACP), racemic 1-phenylethylamine (1-PEA), (YNB) medium agar plates (6.7 g/l YNB without amino acids, (R)-1-PEA, (S)-1-PEA and sodium pyruvate were purchased 15 g/l agar, 20 g/l glucose). from Merck (Hohenbrunn, Germany); (R)-1-phenylethanol and (S)-1-phenylethanol from Sigma-Aldrich (Steinheim, Germany); PLP from AppliChem. When either binds to TAAR1, it reduces dopamine receptor firing rate and triggers protein kinase A (PKA) and protein kinase C (PKC) signaling, resulting in DAT phosphorylation.24] Phosphorylated DAT then either operates in reverse or withdraws into the presynaptic neuron and ceases transport 1. phenylethylamine agonists 2. imidazoline selective a1 agonist 3. guandine selective a2 agonists 4. b2 agonist The pKa is quite different between a benzylic hydroxyl and a phenolic hydroxyl this is apparent. It is just too intriguing that the differences between two so similar materials can have such extremely different charechteristics. geezmeister (Bee of the Month) 12-30-02 17:41 No 394197 : Yields also depend on techniqu

Phényléthylamine — Wikipédi

CHAPTER 22 AMINES SOLUTIONS TO TEXT PROBLEMS 22.1 (b) The amino and phenyl groups are both attached to C-1 of an ethyl group. C6H5CHCH3 NH2 1-Phenylethylamine, or 1-phenylethanamine (c) H2C CHCH2NH2 Allylamine, or 2-propen-1-amine 22.2 N,N-Dimethylcycloheptylamine may also be named as a dimethyl derivative of cycloheptanamine 1 answer. Possible compounds could be: 1-indanone, 2-acetonaphthone, 1-naphthalenemethanol, 2-indanol, 4-phenylcyclohexanone, 9-fluorenone, benzil, 4-biphenylmethanol, 9-fluorenemethanol, 2,2-biphenyldimethanol. 1 answer. Consider the following reaction: 2Al + Fe2O3 --> Al2O 3 + 2Fe. 1 It seems that crystalline porous structure is inclined to provide higher surface area than amorphous materials. 3D COF-DL229, constructed by T d-symmetric 1,3,5,7-tetrakis(4-aminophenyl)-adamantane and (TAPA) and 1,4-phthalaldehyde (PTA) by our group, shows a BET surface area of 1762 m 2 g −1 (Langmuir surface area of 1924 m 2 g −1)

The δ(95Mo) values correlate well with the pKa values for the substituted pyridines; for the n = 1 series, δ(95Mo) ranges from -1053 ppm (pKa = 1.86 for 4-CN) to -1120 ppm (pKa = 9.61 for 4-NMe2). The effects of solvent polarity and some in situ reactivity studies are described and the nature of the Mo-L bond compared to that with piperidine and some other ligands is discussed Chemistry archive containing a full list of chemistry questions and answers from October 02 2018

(R)-(+)-α-Methylbenzylamine 98 % 3886-69-9 Sigma-Aldric

pKa (Strongest Acidic) 1.46: ChemAxon: pKa (Strongest Basic) 9.09: ChemAxon: Physiological Charge: 0: ChemAxon: Hydrogen Acceptor Count: 6: ChemAxon: Hydrogen Donor Count: 4: ChemAxon: Polar Surface Area: 116.14 Å 2: ChemAxon: Rotatable Bond Count: 6: ChemAxon: Refractivity: 88.21 m 3 ·mol-1: ChemAxon: Polarizability: 32.53 Å 3: ChemAxon: Number of Rings: 2: ChemAxon: Bioavailability: 1: ChemAxon: Rule of Fiv John and co-workers developed a multicomponent reaction involving N-protected 3-nitroindole 1 a primary amine 162 and an enolizable ketone 163 for the preparation of a series of functionalized pyrrolo[3,2-b]indoles 164 . 143 It was found that the yield of product 164 decreased to 45% with 1-phenylethylamine Five- and six-coordinate ruthenium(II) complexes containing the bidentate phosphine (-)-N,N-bis(diphenylphosphino)-(S)-1-phenylethylamine [(S)-peap]: X-ray crystal structure of the first 16 electron ruthenium complex bearing a four membered ring [RuCl{k 2-P,P-(S)-peap} 2][SbF 6]·C 2 H 4 Cl 2. J. Díez, M. P. Gamasa, J. G i meno, Y p''K'' a pKa pK a The pK a values of formic acid and the ammonium ion are 3.8 and 9.2, respectively. Acid strength Stability constants of complexes PH Equilibrium constant Dissociation constan Lipase-catalyzed kinetic resolution of (+/-)-1-phenylethylamine with ethyl acetate as an acyl donor was achieved using immobilized lipase (Novozyme 435) as a biocatalyst under microwave irradiation. there is very little experience with pancreas transplantation alone (PTA)

(R)-(+)-α-Phenylethylamine Sigma-Aldric

Fischer projections are another way of visualizing molecules in three dimensions and let's use the example of lactic acids it's called lactic acids it has a carboxylic acid functional group over here on the right and this is the only chirality Center in lactic acids an sp3 hybridized carbon four different substituents attached to it so with only one chirality Center we would expect to have two. Clarke's Analytical Forensic Toxicology Clarke's Analytical Forensic Toxicology Edited by Sue Jickells Adam Negrusz Senior Lecturer, Department of Forensic Science & Drug Monitoring, King's College London, London, U

(S)-(-)-1-Phenylethylamine for the resolution of racemates

The loading amount of lipase and the specific activity got to 132mg/g carrier and 48U/g. The optimal reaction conditions of the acylation reaction using Fe3O4-CTS-glutaraldehyde-lipase were 300mmol/L 1-phenylethylamine, 150mg immobilized lipase, 2mL vinyl acetate, 12.6 ⊥g rotating speed, 40 oC, 8 h 碱性拆分剂:用于拆分酸性化合物 产品 编号 英文名称 中文名称 CAS 包 装 1382 (R)-(+)-1-Phenylethylamine, 99% R-(+)-1-苯 3886-69- 5 77 乙胺 9 g 25 g 10 0 g 25 g 10 1344 (S)-(-)-1- 2627-86- 0 (S)-(-)-1-Phenylethylamine, 99% [ee:98%] 48 苯乙胺 3 g 50 0 g (1S,2R)-(+) 5 1233 (1S,2R)-(+)-2-Amino-1,2-diphenylethanol, -2-氨基 23364-44 g 38 98% [ee:99%] -1,2-二苯基. pKa (Strongest Acidic) 1.69: ChemAxon: pKa (Strongest Basic) 8.84: ChemAxon: Physiological Charge: 0: ChemAxon: Hydrogen Acceptor Count: 8: ChemAxon: Hydrogen Donor Count: 5: ChemAxon: Polar Surface Area: 142.11 Å 2: ChemAxon: Rotatable Bond Count: 9: ChemAxon: Refractivity: 117.43 m 3 ·mol-1: ChemAxon: Polarizability: 43.81 Å 3: ChemAxon: Number of Rings: 3: ChemAxon: Bioavailability: 1: ChemAxon: Rule of Fiv The method of purifying (R)-N-(3,4-dimethoxybenzyl)-1-phenylethylamine comprises adding L-tartaric acid to the (R)-N-(3,4-dimethoxybenzyl)-1-phenylethylamine of reduced purity to obtain (R)-N-(3,4-dimethoxybenzyl)-1-phenylethylamine L-tartrate of high purity as a crystal. - 特許 stereochemical relationship of the products formed by reacting racemic lactic acid with S -1-phenylethylamine

Comparative DFT Analysis of Ligand and Solvent Effects on the Mechanism of H 2 Activation in Water Mediated by Half-Sandwich Complexes [Cp′Ru(PTA) 2 Cl] (Cp′ = C 5 H 5, C 5 Me 5; PTA = 1,3,5-triaza-7-phosphaadamantane) † journal, November 2010. Kovács, Gábor; Rossin, Andrea; Gonsalvi, Luca; Organometallics, Vol. 29, Issue 21; DOI: 10. Acidity coefficient (PKA): 8.14 ± 0.50 (predicted) About The Introduction Of Product: Uses:Liquid crystal intermediate Hsp90 Orchestrates Temperature-Dependent Candida albicans Morphogenesis via Ras1-PKA Signaling. Current Biology, Vol. 19, No. 8. Calcineurin Target CrzA Regulates Conidial Germination, Hyphal Growth, and Pathogenesis of Aspergillus fumigatus. Eukaryotic Cell, Vol. 7, No. 7 A Fischer projection or Fischer projection formula is a convention used to depict a stereoformula in two dimension without destroying the stereochemical information, i.e., absolute configuration, at chiral centers.. eg: (R)-Lactic acidTo convert this stereoformula into a Fischer projection use the following procedure

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