4-Nitrobenzyl alcohol
4-Nitrobenzyl alcohol
  • CAS No.:619-73-8
Other grades of this product :
4-Nitrobenzyl alcohol Basic information
Product Name:4-Nitrobenzyl alcohol
Synonyms:NITROBENZYLALCOHOL(4-);PARA NITRO BENZYL ALCOHOL;P-NITROBENZYL ALCOHOL;RARECHEM AL BD 0193;TIMTEC-BB SBB008259;1-Hydroxymethyl-4-nitrobenaene;4-(Hydroxymethyl)nitrobenzene;4-Nitrobenaylalcohol
CAS:619-73-8
MF:C7H7NO3
MW:153.14
EINECS:210-611-6
Product Categories:FINE Chemical & INTERMEDIATES;Building Blocks;C7 to C8;Chemical Synthesis;Organic Building Blocks;Oxygen Compounds;Benzhydrols, Benzyl & Special Alcohols;Alcohols;C7 to C8;Oxygen Compounds
Mol File:619-73-8.mol
4-Nitrobenzyl alcohol Chemical Properties
Melting point 92-94 °C(lit.)
Boiling point 185 °C12 mm Hg(lit.)
density 1.3585 (rough estimate)
refractive index 1.5030 (estimate)
Fp 180 °C
storage temp. Sealed in dry,Room Temperature
solubility 2g/l
pka13.61±0.10(Predicted)
form Crystalline Powder
color Yellow
Water Solubility Soluble in water (2 mg/ml at 20°C).
BRN 1424026
InChIKeyJKTYGPATCNUWKN-UHFFFAOYSA-N
CAS DataBase Reference619-73-8(CAS DataBase Reference)
NIST Chemistry Reference4-NO2-C6H4CH2OH(619-73-8)
EPA Substance Registry SystemBenzenemethanol, 4-nitro- (619-73-8)
Safety Information
Hazard Codes Xi,C,F,Xn
Risk Statements 36/37/38-34-11-22
Safety Statements 22-24/25-36/37/39-26-45-16
WGK Germany 3
RTECS DP0657100
8
Hazard Note Irritant
TSCA Yes
HS Code 29062900
MSDS Information
ProviderLanguage
p-Nitrobenzyl alcohol English
ACROS English
SigmaAldrich English
ALFA English
4-Nitrobenzyl alcohol Usage And Synthesis
Chemical Propertieswhite to light yellow crystal powde
Uses4-Nitrobenzenemethanol is a potential building block in the synthesis of various pharmaceuticals.
Uses4-nitrobenzyl alcohol is used as the sole source of carbon and nitrogen to study the pathway for the catabolism of 4-nitrotoluene by Pseudomonas.
DefinitionChEBI: 4-nitrobenzyl alcohol is a member of the class of benzyl alcohols that is benzyl alcohol substituted at the para-position by a nitro group. It has a role as a xenobiotic metabolite. It is a member of benzyl alcohols and a C-nitro compound.
Synthesis Reference(s)Organic Syntheses, Coll. Vol. 3, p. 652, 1955The Journal of Organic Chemistry, 55, p. 2968, 1990 DOI: 10.1021/jo00296a078Tetrahedron Letters, 19, p. 4985, 1978
Purification MethodsCrystallise the alcohol from EtOH and sublime it in vacuo. Purity should be at least 99.5%. Sublimed samples should be stored in the dark over anhydrous CaSO4 (Drierite). If the IR contains OH bands, then the sample should be resublimed before use. [Mohammed & Kosower J Am Chem Soc 93 2709 1979, Beilstein 6 IV 2611.]

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