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CAS No 100-51-6 , phenylmethanol

  • Name: phenylmethanol
  • Synonyms: phenylmethanol; alpha-Toluenol; Phenylmethyl alcohol; Benzoyl alcohol; phenylmethanol;benzenemethanol; Hydroxytoluene; Benzenecarbinol; phenylcarbinol;
  • CAS Registry Number:
  • Transport: UN 1593 6.1/PG 3
  • Melting Point: -15 ºC
  • Flash Point: 93 ºC
  • Boiling Point: 205 ºC
  • Density: 1.044
  • Refractive index: 1.538-1.541
  • Water Solubility: 4.29 G/100 ML (20 ºC)
  • Safety Statements: R20/22
  • Hazard Symbols: Xn: Harmful;
  • Flash Point: 93 ºC
  • EINECS: 202-859-9
  • Molecular Weight: 108.13782
  • InchiKey: WVDDGKGOMKODPV-UHFFFAOYSA-N
  • InChI: InChI=1S/C7H8O/c8-6-7-4-2-1-3-5-7/h1-5,8H,6H2
  • Risk Statements: S26
  • Molecular Formula: C7H8O
  • Molecular Structure:CAS No:100-51-6 phenylmethanol
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100-51-6 BENZYL ALCOHOL

  • China Shanghai Sunwise Chemical Co., Ltd. [Manufacturer]
  • Tel: +86-21-64063188
  • Fax: +86-21-64062858
  • Address: Shanghai Sunwise Chemical Co., Ltd.
    7G, No 1235 Wuzhong Road
    Shanghai P.R.China null,nullChina
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100-51-6 (-)-Camphor-10-sulphonic acid

  • (-)-Camphor-10-sulphonic acid
  • Switzerland CONNECT MARKETING GMBH [Manufacturer]
  • Tel: +41 81 740 58 50
  • Fax: +41 81 740 58 51
  • Address: CONNECT MARKETING GMBH
    BAHNWEG NORD 35
    CH-9475 SEVELEN/SG
    SWITZERLAND null,nullSwitzerland
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100-51-6 BENZYL ALCOHOL, 99% PS

  • Spain Panreac Synthesis [Manufacturer]
  • Tel: +34 937 489 400
  • Fax: +34 937 489 494
  • Address: PANREAC QUIMICA, S.A.U.
    Poligono Plan de la Bruguera. Garraf, 2
    E-08211 Castellar del Vall?s
    Barcelona (Spain) null,nullSpain
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100-51-6 02-18201 BENZYL ALCOHOL, NATURAL

  • United States Penta Manufacturing Company [Manufacturer]
  • Tel: (973) 740-2300
  • Fax: (973) 740-1839
  • Address: 50 Okner Parkway
    Livingston, NJ 07039 U.S.A. null,nullUnited States
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100-51-6 Benzyl Alcohol-ring-13C6

  • Benzyl Alcohol-ring-13C6, 99%13C
  • United States Medical Isotopes, Inc. [Manufacturer]
  • Tel: (603) 635-2255/ (800) 374-9513
  • Fax: (603) 635-2448
  • Address: 100 Bridge Street
    Pelham, NH 03076 null,nullUnited States
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100-51-6 BENZYL ALCOHOL

  • United States Graham Chemical Corporation [Manufacturer]
  • Tel: 847-304-4400
  • Fax: 847-304-8752
  • Address: 1250 South Grove Avenue
    Suite 206
    Barrington, Illinois 60010 null,nullUnited States
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100-51-6 Benzylalcohol with gc

  • Benzylalcohol with gcPhenylmethanol
  • United States INDOFINE Chemical Co., Inc. [Manufacturer]
  • Tel: (908) 359-6778
  • Fax: (908) 359-1179
  • Address: 121 Stryker Lane
    Bldg 30, Suite 1
    Hillsborough, NJ 08844 null,nullUnited States
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100-51-6 BENZYL ALCOHOL

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100-51-6 BENZYL ALCOHOL, CHLORINE-FREE

  • United States EMD Chemicals Inc. [Manufacturer]
  • Tel: 800-222-0342/ 856-423-6300
  • Fax: 856-423-4389
  • Address: EMD Chemicals Inc.
    480 South Democrat Road
    Gibbstown, NJ 08027 null,nullUnited States
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100-51-6 Benzyl alcohol

  • China synchem International Co.,Ltd. null
  • Fax: 0086-411-82530108
  • Address: Room 3208/3209 World Trade Center,No.25 TongXing Street,Zhongshan District,Dalian,China. null,nullChina
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References of phenylmethanol
Title: Benzyl Alcohol
CAS Registry Number: 100-51-6
CAS Name: Benzenemethanol
Synonyms: phenylcarbinol; phenylmethanol; a-hydroxytoluene
Molecular Formula: C7H8O
Molecular Weight: 108.14
Percent Composition: C 77.75%, H 7.46%, O 14.80%
Line Formula: C6H5CH2OH
Literature References: Constituent of jasmine, hyacinth, ylang-ylang oils, Peru and Tolu balsams, storax, where it occurs in ester form also. Originally prepd by the Cannizzaro reaction from benzaldehyde + KOH: Cannizzaro, Ann. 88, 129 (1853); cf. Hickinbottom, Reactions of Organic Compds. (Longmans, London, 3rd ed., 1957) p 251; A. I. Vogel, Practical Organic Chemistry (Longmans, London, 3rd ed., 1959) p 711; Gattermann-Wieland, Praxis des Organischen Chemikers (de Gruyter, Berlin, 40th ed., 1961) p 193. Produced on a large scale by the action of sodium or potassium carbonate on benzyl chloride: DE 484662; Chem. Zentralbl. 1930, I, 1052; Frdl. 16, 426; cf. Kirk-Othmer Encyclopedia of Chemical Technology vol. 3 (Interscience, New York, 1964) pp 442-449. Toxicity: Smyth et al., Arch. Ind. Hyg. Occup. Med. 4, 119 (1951).
Properties: Liquid. Faint aromatic odor. Sharp burning taste. d420 1.04535; d425 1.04156. mp -15.19°. bp760 204.7°; bp400 183.0°; bp200 160.0°; bp100 141.7°; bp60 129.3°; bp40 119.8°; bp20 105.8°; bp10 92.6°; bp5 80.8°; bp1.0 58.0°. nD20 1.54035; nD25 1.53837: Dreisbach, Martin, Ind. Eng. Chem. 41, 2875 (1941). Absorption spectrum: Brode, J. Phys. Chem. 30, 61 (1926). Vapor density 3.72 (air = 1.00). Flash pt, closed cup 213°F, open cup 220°F. Autoignition temp 817°F. One gram dissolves in about 25 ml water. One volume dissolves in 1.5 vols of 50% ethyl alcohol. Misc with abs and 94% alcohol, ether, chloroform. LD50 orally in rats: 3.1 g/kg (Smyth).
Melting point: mp -15.19°
Boiling point: bp760 204.7°; bp400 183.0°; bp200 160.0°; bp100 141.7°; bp60 129.3°; bp40 119.8°; bp20 105.8°; bp10 92.6°; bp5 80.8°; bp1.0 58.0°
Flash point: Flash pt, closed cup 213°F, open cup 220°F
Index of refraction: nD20 1.54035; nD25 1.53837: Dreisbach, Martin, Ind. Eng. Chem. 41, 2875 (1941)
Density: d420 1.04535; d425 1.04156
Toxicity data: LD50 orally in rats: 3.1 g/kg (Smyth)
Use: Manuf other benzyl compds. Pharmaceutic aid (antimicrobial). Solvent for gelatin, casein (when hot), solvent for cellulose acetate, shellac. Used in perfumery and in flavoring (mostly in form of its aliphatic esters). In microscopy as embedding material.
Therap-Cat-Vet: Has been used for relief from pruritis.