EU/US Properties Organoleptics Cosmetics Suppliers Safety Safety in use Safety references References Other Blenders Uses Occurrence Synonyms Articles Notes
 

3-butyn-1-ol
2-hydroxyethylacetylene

Supplier Sponsors

Name:but-3-yn-1-ol
CAS Number: 927-74-2Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg:213-161-9
FDA UNII: P74L430293
Nikkaji Web:J1.744B
Beilstein Number:0773710
MDL:MFCD00002955
XlogP3-AA:0.10 (est)
Molecular Weight:70.09102000
Formula:C4 H6 O
BioActivity Summary:listing
NMR Predictor:Predict (works with chrome, Edge or firefox)
Category:natural substances and extractives
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Google Scholar:Search
Google Books:Search
Google Scholar: with word "volatile"Search
Google Scholar: with word "flavor"Search
Google Scholar: with word "odor"Search
Google Patents:Search
US Patents:Search
EU Patents:Search
Pubchem Patents:Search
PubMed:Search
NCBI:Search
 
Physical Properties:
Appearance:colorless to pale yellow clear liquid (est)
Assay: 95.00 to 100.00
Food Chemicals Codex Listed: No
Melting Point: -63.60 °C. @ 760.00 mm Hg
Boiling Point: 129.00 °C. @ 760.00 mm Hg
Vapor Pressure:4.411000 mmHg @ 25.00 °C. (est)
Flash Point: 97.00 °F. TCC ( 36.10 °C. ) (est)
logP (o/w): 0.130 (est)
Soluble in:
 alcohol
 water, 3.821e+005 mg/L @ 25 °C (est)
Insoluble in:
 water
 
Organoleptic Properties:
Odor and/or flavor descriptions from others (if found).
 
Cosmetic Information:
None found
 
Suppliers:
BOC Sciences
For experimental / research use only.
3-Butyn-1-ol 95%
Carbosynth
For experimental / research use only.
3-Butyn-1-ol
Matrix Scientific
For experimental / research use only.
3-Butyn-1-ol, 97%
sds
Santa Cruz Biotechnology
For experimental / research use only.
3-Butyn-1-ol
Sigma-Aldrich: Aldrich
For experimental / research use only.
3-Butyn-1-ol 97%
sds
TCI AMERICA
For experimental / research use only.
3-Butyn-1-ol >97.0%(GC)
sds
 
Safety Information:
Preferred SDS: View
 
Hazards identification
 
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements
 
Pictogram
 
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
intravenous-mouse LD50 100 mg/kg
U.S. Army Armament Research & Development Command, Chemical Systems Laboratory, NIOSH Exchange Chemicals. Vol. NX#05171

Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
 
Safety in Use Information:
Category:
natural substances and extractives
Recommendation for 3-butyn-1-ol usage levels up to:
 not for fragrance use.
 
Recommendation for 3-butyn-1-ol flavor usage levels up to:
 not for flavor use.
 
Safety References:
EPI System: View
AIDS Citations:Search
Cancer Citations:Search
Toxicology Citations:Search
EPA Substance Registry Services (TSCA):927-74-2
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
Laboratory Chemical Safety Summary :13566
National Institute of Allergy and Infectious Diseases:Data
WGK Germany:3
but-3-yn-1-ol
Chemidplus:0000927742
RTECS:ES0710000 for cas# 927-74-2
 
References:
 but-3-yn-1-ol
NIST Chemistry WebBook:Search Inchi
Pubchem (cid):13566
Pubchem (sid):134980765
 
Other Information:
(IUPAC):Atomic Weights of the Elements 2011 (pdf)
Videos:The Periodic Table of Videos
tgsc:Atomic Weights use for this web site
(IUPAC):Periodic Table of the Elements
CHEBI:View
Metabolomics Database:Search
KEGG (GenomeNet):C06146
HMDB (The Human Metabolome Database):Search
Export Tariff Code:2905.29.9000
VCF-Online:VCF Volatile Compounds in Food
ChemSpider:View
 
Potential Blenders and core components note
None Found
 
Potential Uses:
None Found
 
Occurrence (nature, food, other):note
 found in nature
 
Synonyms:
 but-3-yn-1-ol
2-hydroxyethylacetylene
 

Articles:

PubMed:Reactivity of Cl atom with triple-bonded molecules. An experimental and theoretical study with alcohols.
PubMed:The beta3-adrenoceptor agonist 4-[[(Hexylamino)carbonyl]amino]-N-[4-[2-[[(2S)-2-hydroxy-3-(4-hydroxyphenoxy)propyl]amino]ethyl]-phenyl]-benzenesulfonamide (L755507) and antagonist (S)-N-[4-[2-[[3-[3-(acetamidomethyl)phenoxy]-2-hydroxypropyl]amino]-ethyl]phenyl]benzenesulfonamide (L748337) activate different signaling pathways in Chinese hamster ovary-K1 cells stably expressing the human beta3-adrenoceptor.
PubMed:Long-term but not short-term p38 mitogen-activated protein kinase inhibition improves cardiac function and reduces cardiac remodeling post-myocardial infarction.
PubMed:A novel approach toward asymmetric synthesis of alcohol functionalized C-chiral diphosphines via two-stage hydrophosphination of terminal alkynols.
PubMed:Calorimetric and computational study of 3-buten-1-ol and 3-butyn-1-ol. Estimation of the enthalpies of formation of 1-alkenols and 1-alkynols.
PubMed:Synthesis, characterisation and molecular structure of Re(III) 2-oxacyclocarbenes stabilised by a benzoyldiazenido ligand.
PubMed:3-(4-Aminobutyn-1-yl)pyridines: binding at alpha 4 beta 2 nicotinic cholinergic receptors.
PubMed:Total synthesis of (+/-)-kainic Acid with an aza-[2,3]-Wittig sigmatropic rearrangement as the key stereochemical determining step.
PubMed:RWJ 67657, a potent, orally active inhibitor of p38 mitogen-activated protein kinase.
PubMed:Lipase specificity toward some acetylenic and olefinic alcohols in the esterification of pentanoic and stearic acids.
PubMed:Ion-molecule reactions and collision-activated dissociation of C4H 4 (+.) isomers: A case study in the use of the MS (3) capabilities of a pentaquadrupole mass spectrometer.
PubMed:Replacement of carcinogenic alkylating agent ethylene oxide in the synthesis of (Z)-3-dodecen-1-YL (E)-2-butenoate, sex pheromone of sweet-potato weevil,Cylas formicarius elegantulus (summers) andCylas formicarius formicarius (F.).
PubMed:The toxicity of acetylenic alcohols to the fathead minnow, Pimephales promelas: narcosis and proelectrophile activation.
PubMed:Stereospecific synthesis of (Z,Z)-3,5-tetradecadienoic acid, a component ofAttagenus elongatulus (Casey) pheromone.
PubMed:Inactivation of alcohol dehydrogenase by 3-butyn-1-ol.
 
Notes:
alcohol dehydrogenase inactivator.
Please share your Comments.
Email Address:
Top of Page Home
Copyright © 1980-2021 The Good Scents Company (tgsc) ™ Disclaimer Privacy Policy