U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C4H10O
Molecular Weight 74.1216
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BUTYL ALCOHOL

SMILES

CCCCO

InChI

InChIKey=LRHPLDYGYMQRHN-UHFFFAOYSA-N
InChI=1S/C4H10O/c1-2-3-4-5/h5H,2-4H2,1H3

HIDE SMILES / InChI

Molecular Formula C4H10O
Molecular Weight 74.1216
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Sodium butoxide (Sodium butanolate) is used in wide range of applications in organic synthesis; agrochemicals; pharmaceuticals, colorants and aroma chemicals. It can also be used in manufacturing detergents, as a catalyst in polymerization and isomerizations.

Approval Year

PubMed

PubMed

TitleDatePubMed
Respiratory burst response of peritoneal leukocytes adhering to titanium and stainless steel.
2001-11
Involvement of phospholipase D in sphingosine 1-phosphate-induced activation of phosphatidylinositol 3-kinase and Akt in Chinese hamster ovary cells overexpressing EDG3.
2001-09-21
Antimicrobial activity of Alstonia macrophylla: a folklore of bay islands.
2001-09
Phospholipase D is required in the signaling pathway leading to p38 MAPK activation in neutrophil-like HL-60 cells, stimulated by N-formyl-methionyl-leucyl-phenylalanine.
2001-08-24
Novel lipase-catalysed enantioselective deacetylation of (+/-)-5-acetoxy-3-(4-fluorophenyl)-2-phenylisoxazolidine.
2001-08-20
Nootropic and anxiolytic activity of saponins of Albizzia lebbeck leaves.
2001-08-18
Isolation of praeruptorins A and B from Peucedanum praeruptorum Dunn. and their general pharmacological evaluation in comparison with extracts of the drug.
2001-08-03
DNA adduct formation by the ubiquitous environmental contaminant 3-nitrobenzanthrone in rats determined by (32)P-postlabeling.
2001-08-01
Suppression of chemical mutagen-induced SOS response by alkylphenols from clove (Syzygium aromaticum) in the Salmonella typhimurium TA1535/pSK1002 umu test.
2001-08
Purification and characterization of molybdenum species from Medicago sativa (alfalfa) grown on mine tailings.
2001-08
Evaluation of the potency activity of aphrodisiac in Eurycoma longifolia Jack.
2001-08
Contribution of heat shock proteins to cell protection from complement-mediated lysis.
2001-08
Antibacterial activity of Marula (Sclerocarya birrea (A. rich.) Hochst. subsp. caffra (Sond.) Kokwaro) (Anacardiaceae) bark and leaves.
2001-08
Evaluation of subchronic toxicity of n-butyl acetate vapor.
2001-08
Tuning lipase enantioselectivity in organic media using solid-state buffers.
2001-07-27
Temperature and viscosity dependence in the stereoselective formation of the inverted housane for the photochemical nitrogen loss from the deuterium-stereolabeled parent diazabicyclo[2.2.1]hept-2-ene.
2001-07-25
Rapid high-performance liquid chromatographic method for the simultaneous determination of retinol, alpha-tocopherol and beta-carotene in human plasma and low-density lipoproteins.
2001-07-15
Separation of hydrophobic polymer additives by microemulsion electrokinetic chromatography.
2001-07-13
Antifungal activity of Artemisia annua endophyte cultures against phytopathogenic fungi.
2001-07-12
Influence of hydrogel structure on the processes of water penetration and drug release from mixed hydroxypropylmethyl cellulose/thermally pregelatinized waxy maize starch hydrophilic matrices.
2001-07-03
Azurin involved in alcohol oxidation system in Pseudomonas putida HK5: expression analysis and gene cloning.
2001-07
Quantification of butanol and ethanol in aqueous phases by reflectometric interference spectroscopy--different approaches to multivariate calibration.
2001-07
Induction of butane consumption in Pseudomonas butanovora.
2001-07
Quick regiospecific analysis of fatty acids in triacylglycerols with GC using 1,3-specific lipase in butanol.
2001-07
Phosphatidylcholine-specific phospholipase C and D in stimulation of RAW264.7 mouse macrophage-like cells by lipopolysaccharide.
2001-07
Effects of dietary supplementation with Yucca schidigera Roezl ex Ortgies and its saponin and non-saponin fractions on rat metabolism.
2001-07
Straight-chain alcohols exhibit a cutoff in potency for the inhibition of recombinant glutamate receptor subunits.
2001-07
Improved determination of tributyl phosphate degradation products (mono- and dibutyl phosphates) by ion chromatography.
2001-06-22
Occurrence of 1,4-dioxane in cosmetic raw materials and finished cosmetic products.
2001-06-22
Calorimetric and Fourier transform infrared spectroscopic study of solid proteins immersed in low water organic solvents.
2001-06-11
Effects of the butylated hydroxyanisole and butylated hydroxytoluene on the DNA adduct formation and arylamines N-acetyltransferase activity in human colon tumor cells.
2001-06-09
Phosphatidic acid activates a wound-activated MAPK in Glycine max.
2001-06
Potentiation of nerve growth factor-induced elongation of neurites by gelsemiol and 9-hydroxysemperoside aglucone in PC12D cells.
2001-06
Long-term administration of N-acetylcysteine decreases hydrogen peroxide exhalation in subjects with chronic obstructive pulmonary disease.
2001-06
Phosphatidylcholine-specific phospholipase C regulates activation of RAW264.7 macrophage-like cells by lipopeptide JBT3002.
2001-06
A role for the Swe1 checkpoint kinase during filamentous growth of Saccharomyces cerevisiae.
2001-06
Studies on the biosynthesis of 2-hydroxy-1,4-benzoxazin-3-one (HBOA) from 3-hydroxyindolin-2-one in Zea mays.
2001-06
Vasopressin-stimulated Ca2+ spiking in vascular smooth muscle cells involves phospholipase D.
2001-06
Studies on the use of Yucca schidigera to control giardiosis.
2001-05-22
Wet effluent diffusion denuder technique and determination of volatile organic compounds in air. I. Oxo compounds (alcohols and ketones).
2001-05-18
Study of retention in micellar liquid chromatography on a C8 column by the use of linear solvation energy relationships.
2001-05-18
Direct quantitative analysis of lysophosphatidic acid molecular species by stable isotope dilution electrospray ionization liquid chromatography-mass spectrometry.
2001-05-15
Extremely high electric field strengths in non-aqueous capillary electrophoresis.
2001-05-04
Kinetic regulation of an alkaline p-nitrophenylphosphate phosphatase from Halobacterium salinarum in low water system by Mn2+ and monovalent cations.
2001-05-01
Soy molasses as fermentation substrate for production of butanol using Clostridium beijerinckii BA101.
2001-05
Antibacterial activity of Picrasma javanica.
2001-05
Interactions between artificial saliva and 20 aroma compounds in water and oil model systems.
2001-05
Studies on the effect of alcohols on the chiral discrimination mechanisms of amylose stationary phase on the enantioseparation of nebivolol by HPLC.
2001-04-24
Separation of neutral compounds by microemulsion electrokinetic chromatography: fundamental studies on selectivity.
2001-04
Relationship of properties of polycyclic aromatic hydrocarbons to sequestration in soil.
2001
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 17:34:31 GMT 2025
Edited
by admin
on Mon Mar 31 17:34:31 GMT 2025
Record UNII
8PJ61P6TS3
Record Status Validated (UNII)
Record Version
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Name Type Language
BUTYL ALCOHOL
FCC   FHFI   HSDB   II   MART.  
Systematic Name English
N-BUTYL ALCOHOL
INCI   MI   WHO-DD  
INCI  
Preferred Name English
1-BUTANOL [USP-RS]
Common Name English
BUTYL ALCOHOL [HSDB]
Common Name English
ALCOHOL,BUTYL [VANDF]
Common Name English
BUTYL ALCOHOL [MART.]
Common Name English
ALCOHOL,BUTYL
VANDF  
Common Name English
ALCOHOL, BUTYL
Systematic Name English
FEMA NO. 2178
Code English
N-BUTYL ALCOHOL [MI]
Common Name English
BUTYL ALCOHOL [FHFI]
Common Name English
NSC-62782
Code English
N-butyl alcohol [WHO-DD]
Common Name English
BUTAN-1-OL
Systematic Name English
BUTYL ALCOHOL [FCC]
Common Name English
BUTYL ALCOHOL [II]
Common Name English
TRIBUTYL ACETYLCITRATE IMPURITY D [EP IMPURITY]
Common Name English
METHYLOLPROPANE
Systematic Name English
N-BUTANOL
Common Name English
1-BUTANOL
USP-RS  
Systematic Name English
PROPYLCARBINOL
Systematic Name English
Classification Tree Code System Code
CFR 21 CFR 175.320
Created by admin on Mon Mar 31 17:34:31 GMT 2025 , Edited by admin on Mon Mar 31 17:34:31 GMT 2025
CFR 21 CFR 172.515
Created by admin on Mon Mar 31 17:34:31 GMT 2025 , Edited by admin on Mon Mar 31 17:34:31 GMT 2025
JECFA EVALUATION BUTYL ALCOHOL
Created by admin on Mon Mar 31 17:34:31 GMT 2025 , Edited by admin on Mon Mar 31 17:34:31 GMT 2025
Code System Code Type Description
NCI_THESAURUS
C45678
Created by admin on Mon Mar 31 17:34:31 GMT 2025 , Edited by admin on Mon Mar 31 17:34:31 GMT 2025
CONCEPT Industrial Aid
CAS
71-36-3
Created by admin on Mon Mar 31 17:34:31 GMT 2025 , Edited by admin on Mon Mar 31 17:34:31 GMT 2025
PRIMARY
WIKIPEDIA
N-BUTANOL
Created by admin on Mon Mar 31 17:34:31 GMT 2025 , Edited by admin on Mon Mar 31 17:34:31 GMT 2025
PRIMARY
MERCK INDEX
m2812
Created by admin on Mon Mar 31 17:34:31 GMT 2025 , Edited by admin on Mon Mar 31 17:34:31 GMT 2025
PRIMARY Merck Index
EVMPD
SUB12536MIG
Created by admin on Mon Mar 31 17:34:31 GMT 2025 , Edited by admin on Mon Mar 31 17:34:31 GMT 2025
PRIMARY
NSC
62782
Created by admin on Mon Mar 31 17:34:31 GMT 2025 , Edited by admin on Mon Mar 31 17:34:31 GMT 2025
PRIMARY
DAILYMED
8PJ61P6TS3
Created by admin on Mon Mar 31 17:34:31 GMT 2025 , Edited by admin on Mon Mar 31 17:34:31 GMT 2025
PRIMARY
EVMPD
SUB12537MIG
Created by admin on Mon Mar 31 17:34:31 GMT 2025 , Edited by admin on Mon Mar 31 17:34:31 GMT 2025
PRIMARY
MESH
D020001
Created by admin on Mon Mar 31 17:34:31 GMT 2025 , Edited by admin on Mon Mar 31 17:34:31 GMT 2025
PRIMARY
SMS_ID
100000092893
Created by admin on Mon Mar 31 17:34:31 GMT 2025 , Edited by admin on Mon Mar 31 17:34:31 GMT 2025
PRIMARY
EPA CompTox
DTXSID1021740
Created by admin on Mon Mar 31 17:34:31 GMT 2025 , Edited by admin on Mon Mar 31 17:34:31 GMT 2025
PRIMARY
CHEBI
28885
Created by admin on Mon Mar 31 17:34:31 GMT 2025 , Edited by admin on Mon Mar 31 17:34:31 GMT 2025
PRIMARY
ECHA (EC/EINECS)
200-751-6
Created by admin on Mon Mar 31 17:34:31 GMT 2025 , Edited by admin on Mon Mar 31 17:34:31 GMT 2025
PRIMARY
RXCUI
1310579
Created by admin on Mon Mar 31 17:34:31 GMT 2025 , Edited by admin on Mon Mar 31 17:34:31 GMT 2025
PRIMARY RxNorm
HSDB
47
Created by admin on Mon Mar 31 17:34:31 GMT 2025 , Edited by admin on Mon Mar 31 17:34:31 GMT 2025
PRIMARY
PUBCHEM
263
Created by admin on Mon Mar 31 17:34:31 GMT 2025 , Edited by admin on Mon Mar 31 17:34:31 GMT 2025
PRIMARY
RS_ITEM_NUM
1081807
Created by admin on Mon Mar 31 17:34:31 GMT 2025 , Edited by admin on Mon Mar 31 17:34:31 GMT 2025
PRIMARY
DRUG BANK
DB02145
Created by admin on Mon Mar 31 17:34:31 GMT 2025 , Edited by admin on Mon Mar 31 17:34:31 GMT 2025
PRIMARY
FDA UNII
8PJ61P6TS3
Created by admin on Mon Mar 31 17:34:31 GMT 2025 , Edited by admin on Mon Mar 31 17:34:31 GMT 2025
PRIMARY
ChEMBL
CHEMBL14245
Created by admin on Mon Mar 31 17:34:31 GMT 2025 , Edited by admin on Mon Mar 31 17:34:31 GMT 2025
PRIMARY
JECFA MONOGRAPH
6
Created by admin on Mon Mar 31 17:34:31 GMT 2025 , Edited by admin on Mon Mar 31 17:34:31 GMT 2025
PRIMARY
NCI_THESAURUS
C76700
Created by admin on Mon Mar 31 17:34:31 GMT 2025 , Edited by admin on Mon Mar 31 17:34:31 GMT 2025
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
SALT/SOLVATE -> PARENT
Related Record Type Details
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (GC)
EP
Related Record Type Details
ACTIVE MOIETY