N N-Dimethylpropylamine

N N-DIMETHYLPROPYLAMINE Issue 3 0 – 1 February 2017 1 / 14 SECTION 1: Identification of the substance/mixture and of the company/undertaking 1 1 Product identifier Chemical name: N N-dimethylpropane-1-amine Registration number: 01-2119977070-40-0002 Index number: – EC number (EINECS): 213-139-9 CAS number: 926-63-6 Other names: Dimethyl(propyl)amine 1 2 Relevant An aqueous solvent composition is provided comprising a nucleophilic component having one or more sterically unhindered primary or secondary amine moieties a Brnsted base component having one or more basic nitrogen moieties a water-soluble organic solvent and water A biphasic composition is provided comprising one or more carbamate compounds one or more conjugate acids of Brnsted

displaying diverse framework topologies Solvent

H3PO4 (85 wt% 135 μl) H2C2O42H2O (0 252 g) and 3 3′-iminobis(N N-dimethylpropylamine) (114 μl) was sealed in a Teflon-lined stainless steel autoclave and heated at 150 C for 7 days The autoclave was subsequently allowed to cool to room temperature Colorless crystals were recovered by filtration washed with distilled

N N-Dimethylpropylamine 【Synonyms】 Dimethyl(propyl)amine Dimethylammonium propane N N-Dimethyl-n-propylamine N N-Dimethylpropylamine Propyldimethylamine 【CAS】 926-63-6 【Formula】 C5H13N 【Molecular Weight】 87 16 【EINECS】 213-139-9 【Beilstein/Gmelin】 1730931 【Beilstein Reference】 4-04-00-00467: Physical and Chemical Properties: Back to Contents

ChEBI Name chlorphenamine: ChEBI ID CHEBI:52010: Definition A tertiary amino compound that is propylamine which is substituted at position 3 by a pyridin-2-yl group and a p-chlorophenyl group and in which the hydrogens attached to the nitrogen are replaced by methyl groups

3-(2-Chloro-10H-phenothiazin-10-yl)-N N-dimethylpropylamine monohydrochloride C 17 H 19 ClN 2 S・HCl 355 33 ?のので においはないか はわずかになにおいがある.にめてけやすく エタノール(95)は(100)にけやすく にややけにくく

668104 25277-18-3 3-Ethoxy-N N-dimethylpropylamine EINECS 246-786-0 Smiles: O(CC)CCCN(C)C pdb file: 668104 pdb sdf file: 668104 sdf Please note: images may show incorrect connectivity due to improper geometry We will be working to improve this situation For now the left image should be correct and the other two are correct if they match

Frster Resonance Energy Transfer‐Activated Processes in

After reaction completion residual 3 3′‐iminobis(N N‐dimethylpropylamine was removed in vacuo followed by dissolution of the crude products in acetone filtration and solvent evaporation under reduced pressure Yield of C 12 (DAPA) 2: 87 65 % The obtained intermediate (14 80 g 40 mmol) was allowed to react with 0 5 m HCl (200 mL) at 5 C for 5 h and the resulting product C 12

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Mae clorffenamin sydd hefyd yn cael ei alw'n clorffeniramin (USAN a'r BAN blaenorol) neu'n CP sy'n cael ei farchnata'n aml ar ffurf clorffenamin malead yn wrth-histamin alcylamin cenhedlaeth gyntaf a ddefnyddir i atal symptomau anhwylderau alergaidd fel rhinitis a'r ddanadfrech Y fformiwla cemegol ar gyfer y cyffur hwn yw C₁₆H₁₉ClN₂

アミトリプチリン10mg「サワイ」 :1にアミトリプチリン10mgをする。 として、カルナウバロウ、カルメロースCa、セルロース、チタン、ステアリンMg、、ヒドロキシプロピルセルロース、ヒプロメロース、マクロゴール6000、1アルミニウム

3-Chloro-2-methyl-N N-dimethylpropylamine hydrochloride SDS Certificate of Analysis Product Specification Technical Inquiry Stock No Size Price ($) Quantity Availability L06091-14: 25g: 19 30: L06091-22: 100g: 53 80: L06091-36: 500g: 199 00: Add to Cart Bulk/Specialty Print Quote View Item Product Overview Health Safety Documentation 3-Dimethylamino-2-methylpropyl chloride

This project is supported by the Canadian Institutes of Health Research (award #111062) Alberta Innovates - Health Solutions and by The Metabolomics Innovation Centre (TMIC) a nationally-funded research and core facility that supports a wide range of cutting-edge metabolomic studies TMIC is funded by Genome Alberta Genome British Columbia and Genome Canada a not-for-profit organization

General description N N-Dimethylbutylamine is a tertiaryalkylamine X-ray photoelectron spectra (XPS) of Si(001) surfaces exposed to N N-dimethylbutylamine at 300K has been reported Application N N-Dimethylbutylamine is suitable for use in the fabrication of polystyrene-based nano-LC monolithic columns for the separation of protein molecules

N N-Dimethylpropylamine Hygine et scurit Proprits physiques 1 Mise jour : 2002-07-09 tat physique : Liquide: Masse molculaire : 102 21: Densit de vapeur (air=1) : 3 52: Point d'bullition : 133 C: Tension de vapeur : 5 mm de Hg (1 kPa) 20 C Autre(s) valeur(s) : 18 mm 37 7 C : Concentration saturation : 7 000 ppm: Facteur de conversion (ppm-mg/m) :

Brompheniramine maleate

This project is supported by the Canadian Institutes of Health Research (award #111062) Alberta Innovates - Health Solutions and by The Metabolomics Innovation Centre (TMIC) a nationally-funded research and core facility that supports a wide range of cutting-edge metabolomic studies TMIC is funded by Genome Alberta Genome British Columbia and Genome Canada a not-for-profit organization

668104 25277-18-3 3-Ethoxy-N N-dimethylpropylamine EINECS 246-786-0 Smiles: O(CC)CCCN(C)C pdb file: 668104 pdb sdf file: 668104 sdf Please note: images may show incorrect connectivity due to improper geometry We will be working to improve this situation For now the left image should be correct and the other two are correct if they match

A new process for the preparation of 3-N N-dimethylaminopropylthio derivatives of heterocycles by reaction of the mercapto compound with 3-chloro-N N-dimethylpropylamine in ethanolic ammonia has been shown to give more reliable and improved results Of the compounds examined for amplification of the activity of phleomycin N N-dimethyl- 3-(2-methylthiazolo[4 5-pyrazin-6-ylthio)propylamine and

3-Chloro-N N-dimethylpropylamine hydrochloride 3-Dimethylaminopropyl chloride HCL DMPC HCl 3-chloropropyldimethylammonium chloride hcl 3-Dimethylaminorpopyl chloride hydrochloride 1-Chloro-3-dimethylaminopropane hydrochloride 3-chloro-N N-dimethylpropan-1-aminium hcl 3-Chloro-N N-Dimethylpropylamine HCL

After reaction completion residual 3 3′‐iminobis(N N‐dimethylpropylamine was removed in vacuo followed by dissolution of the crude products in acetone filtration and solvent evaporation under reduced pressure Yield of C 12 (DAPA) 2: 87 65 % The obtained intermediate (14 80 g 40 mmol) was allowed to react with 0 5 m HCl (200 mL) at 5 C for 5 h and the resulting product C 12

N N-Dimethylpropylamine DIMETHYLPROPYLAMINE 926-63-6 Dimethyl(propyl)amine N N-dimethylpropan-1-amine More Molecular Weight: 87 16 g/mol Dates: Modify: 2020-06-13 Create: 2005-03-27 Dimethyl-n-propylamine appears as a colorless liquid Less dense than water Contact may irritate skin eyes and mucous membranes May be toxic by ingestion Used to make other chemicals

CAS: 5407-04-5: Molecular Formula: C5H13Cl2N: Molecular Weight (g/mol) 158 07: MDL Number: MFCD00012521: InChI Key: LJQNMDZRCXJETK-UHFFFAOYSA-N: Synonym: 3-chloro-n n-dimethylpropan-1-amine hydrochloride 3-chloro-n n-dimethylpropylamine hydrochloride 3-chloropropyl dimethylamine hydrochloride 3-dimethylamino propyl chloride hydrochloride 3-dimethylaminopropyl

:3- (3-Chloro-10 11-dihydro- 5H-dibenzo[b f ]azepin-5- yl)-N N-dimethylpropylamine monohydrochloride : :C19H23ClN2・HCl :351 31 :~のので、においはない。 (100)にめてけやすく、、メタノールはクロロホルム にけやすく、エタノール(95

N N-Dimethylpropylamine Hygine et scurit Proprits physiques 1 Mise jour : 2002-07-09 tat physique : Liquide: Masse molculaire : 102 21: Densit de vapeur (air=1) : 3 52: Point d'bullition : 133 C: Tension de vapeur : 5 mm de Hg (1 kPa) 20 C Autre(s) valeur(s) : 18 mm 37 7 C : Concentration saturation : 7 000 ppm: Facteur de conversion (ppm-mg/m) :

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