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Detail of "100-60-7"

  • CAS Number:
  • 100-60-7
  • Name:
  • Cyclohexanamine,N-methyl-

  • Superlist Name:
  • N-Methylcyclohexylamine
  • Molecular Structure:
  • Formula:
  • C7H15N
  • Molecular Weight:
  • 113.2
  • Synonyms:
  • Cyclohexylamine,N-methyl- (6CI,7CI,8CI);(Methylamino)cyclohexane;Cyclohexylmethylamine;Methylcyclohexylamine;N-Cyclohexyl-N-methylamine;N-Cyclohexylmethylamine;N-Methyl-N-cyclohexylamine;N-Methylcyclohexanamine;NSC 434;
  • EINECS:
  • 202-869-3
  • Density:
  • 0.868 g/cm3
  • Melting Point:
  • -9--7 °C(lit.)
  • Boiling Point:
  • 146.5 °C at 760 mmHg
  • Flash Point:
  • 29.4 °C
  • Solubility:
  • 5.4 g/100 mL (20 °C) in water
  • Appearance:
  • clear colourless to yellow liquid
  • Hazard Symbols:
  • CorrosiveC
  • Risk Codes:
  • 10-21/22-35-20/21/22
  • Safety:
  • 16-26-36/37/39-45 Details
  • Transport Information:
  • UN 2734 8/PG 2

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CAS No.100-60-7 N-Methylcyclohexylamine

Assay:98.5% min  Appearance:clear colore...

Product name:N-Methylcyclohexylamine Water:0.5% max

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CAS No.100-60-7 N-Methylcyclohexylamine

Assay:98%

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CAS No.100-60-7 N-Methylcyclohexylamine

N-METHYL CYCLOHEXYLAMINE---We supply this product in very competitive price.

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CAS No.100-60-7 N-Methylcyclohexylamine

Assay:99.0% Min.

Supplier:ORCHID CHEMICAL SUPPLIES LTD (OCS) [ China (Mainland)]

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CAS No.100-60-7 N-Methylcyclohexylamine

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CAS No.100-60-7 N-Methylcyclohexylamine

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CAS No.100-60-7 N-Methylcyclohexylamine

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CAS No.100-60-7 N-Methylcyclohexylamine

Assay:≥ 99%  Appearance:colorless or...  Package:180kg drum

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CAS No.100-60-7 N-Methylcyclohexylamine

N-Cyclohexylmethylamine

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CAS No.100-60-7 N-Methylcyclohexylamine

ChemaicalName N-Methvlcyclohexylamine Molecular weight 113 StructureFormula Properties Molecular formula:C7H15N Appearance:colorless to yellowish clear liquid Boiling point(℃):148-151 Relative density(20℃):0.8680±0.0005 Refraction index(20℃):1.4560 Purity%:≥99 Flash

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CAS No.100-60-7 N-Methylcyclohexylamine

Assay:≥99%

Product with competitive price and high quality;Your inquiry will be highly appreciated!

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CAS No.100-60-7 N-Methylcyclohexylamine

Product explanation Common name: N-Methvlcyclohexylamine Structural fromula:C7H15N=113 Physical and chemical properties: Colourless to yellowish clear liquid Main uses: This product is used as intermediate compound of drug(salt of hexanamine bromide hydrogen chloride

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CAS No.100-60-7 N-Methylcyclohexylamine

CAS Registry No. 100-60-7 Molecular Weight 113 Empirical Formula C7H15N TYPICAL PHYSICAL PROPERTIES Form @15°C : Colourless to light yellow liquid. Specific Gravity @ 25°C : 0.868 Flash Point : 39°C Boiling Point : 149

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CAS No.100-60-7 N-Methylcyclohexylamine

N-Methylcyclohexylamine

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CAS No.100-60-7 N-Methylcyclohexylamine

N-Methylcyclohexylamine

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CAS No.100-60-7 N-Methylcyclohexylamine

N-Methylcyclohexylamine

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CAS No.100-60-7 N-Methylcyclohexylamine

N-Methyl cyclohexylamine

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CAS No.100-60-7 N-Methylcyclohexylamine

N-METHYLCYCLOHEXYLAMINE

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CAS No.100-60-7 N-Methylcyclohexylamine

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CAS No.100-60-7 N-Methylcyclohexylamine

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CAS No.100-60-7 N-Methylcyclohexylamine

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Reference

Effects of nitrogen compounds on deposit formation during synfuel storage
Frankenfeld, John W.; Taylor, William F. (Exxon Res. Eng. Co., Linden, NJ 07036, USA). Prepr. Pap. - Am. Chem. Soc., Div. Fuel Chem., 23(4), 205-14 (English) 1978. CODEN: ACFPAI. ISSN: 0569-3772. DOCUMENT TYPE: Journal CA Section: 51 (Fossil Fuels, Derivatives, and Related Products) Section cross-reference(s): 23, 28 The effects of storage conditions on the stability of purified decane contg. various org. N compds. were studied exptl. to gain information related to the stability of synthetic fuels (e.g., shale oil) that contain relatively large amts. of N compds. Prolonged storage tests (£60 days) were carried out with decane [124-18-5] solns. (2000 ppm N content) of the following N compds.: 2,5-dimethylpyrrole (I) [625-84-3], indole [120-72-9], carbazole [86-74-8], 2,4,6-trimethylpyridine [108-75-8], quinoline [91-22-5], 2,6-dimethylaniline [87-62-7], hexylamine [111-26-2], methylcyclohexylamine [100-60-7], 2-methylpiperidine [109-05-7], and caproamide [628-02-4]. Only the 1st 3 compds., which are pyrrole-type compds., produced significant amts. of sediment, with I giving the largest amt. The formation of sediment in I-contg. decane was accelerated by sunlight and UV irradn. and by the presence of decanoic acid [334-48-5] or cyclohexanecarboxylic acid [98-89-5] (at 500 ppm O concn.). Phenols inhibited sediment formation, with 2,6-di-tert-butylphenol [128-39-2] being the most effective of those tested. Based on elemental analyses, IR spectra, and mass spectra the sediments produced by I are apparently low-to-medium mol. wt. oligomers consisting of partially oxidized repeating units of the compd.
High purity formulations of highly substituted lithium amide bases
High purity formulations of highly substituted lithium amide bases. Hall, Randy W.; Wedinger, Robert S.; Rathman, Terry L.; Schwindeman, James A. (FMC Corp., USA). PCT Int.There are some reagents like 100-60-7 is used in this study. Appl. WO 9706173 A1 20 Feb 1997, 12 pp. DESIGNATED STATES: W: AL, AM, AT, AU, AZ, BB, BG, BR, BY, CA, CH, CN, CZ, DE, DK, EE, ES, FI, GB, GE, HU, IL, IS, JP, KE, KG, KP, KR, KZ, LK, LR, LS, LT, LU, LV, MD, MG, MK, MN, MW, MX, NO, NZ, PL, PT, RO, RU, SD, SE, SG, SI, SK, TJ, TM, TR, TT, UA, UG, UZ, VN, AM, AZ, BY, KG, KZ, MD, RU, TJ, TM; RW: AT, BE, BF, BJ, CF, CG, CH, CI, CM, DE, DK, ES, FI, FR, GA, GB, GR, IE, IT, LU, MC, NL, PT, SE. (English). (World Intellectual Property Organization). CODEN: PIXXD2. CLASS: ICM: C07F001-00. ICS: C07F007-10; C07C209-66; C07C211-00. APPLICATION: WO 1996-US12895 8 Aug 1996. PRIORITY: US 1995-2059 9 Aug 1995; US 1996-620587 22 Mar 1996. DOCUMENT TYPE: Patent CA Section: 29 (Organometallic and Organometalloidal Compounds) Section cross-reference(s): 21 A process for prepg. high purity solns. of highly substituted lithium amide bases by direct reaction of lithium metal with highly substituted amine bases alone or in an ether solvent, a hydrocarbon solvent or in a mixed ether/hydrocarbon solvent mixt., optionally in the presence of a catalyst selected from tin salts and transition metal salts of Groups 4B, 5B, 6B, 7B, and 8 of the Periodic Table is described. .
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