1,8-octane diol
1,8-dihydroxyoctane
 
Notes:
None found
  • BOC Sciences
    • BOC Sciences
      Best of Chemicals Supplier
      Quality supplier of research chemicals and biochemicals including inhibitors, building blocks, GMP Products, impurities and metabolites, APIs for Veterinary, Natural Compounds, ADCs, Stem Cell Molecule and chiral compounds.
      BOC Sciences provides a wide range of services to support the pharmaceutical industry through all stages of drug discovery including Custom Synthesis of those chemicals that are not in stock, Isotope Labeling Service, Chiral Synthesis and Resolution, Bioconjugation, PEGylation services, analytical services.
      BOC Sciences is a brand of BOCSCI Inc. We leverage our wide spectrum of business in the fields of development, manufacturing, marketing, and distribution to help you make best-informed decisions tailored to your evolving needs for premium chemicals. Our complete suite of CRO services spans the entire molecule development pipeline including contract research for target identification, building blocks, compound synthesis, biochemical and cellular analysis, preclinical animal tests, and clinical studies.
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      Product(s):
      629-41-4 1,8-octanediol 96%
       
  • Jiangyin Healthway
    • Jiangyin Healthway International Trade Co., Ltd
      Independent Ingredients Supplier
      We provide custom synthesis and contract manufacturing from milligrams to metric tonnes.
      Jiangyin Healthway International Trade Co., Ltd is a professional company, main engaged in manufacturing and exporting aroma chemicals ,food additives , cosmetic ingredient ,pharmaceutical intermediates & other fine chemicals; especially on aroma chemicals , as the major manufacturer of heterocyclic and sulphur aroma compounds , we are the leading independent ingredients supplier to the flavour and fragrance industries in China, can offer hundreds of different high quality aroma chemicals.
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      Services
      Biochemical
      Natural Food Colour
      New functional food ingredients
      Product(s):
      HLW-FC083 1,8-Octanediol
       
  • TCI AMERICA
    • TCI AMERICA
      Moving Your Chemistry Forward
      We continuously strive to advance our technology.
      With East & West Coast distribution centers, count on TCI to deliver products quickly and reliably. Over 30,000 Reagents available today in benchtop to bulk quantities. We also offer custom synthesis solutions. Sign up for a TCI account today for fast and free shipping!
      Tokyo Chemical Industry Co., Ltd. (TCI) is a leading worldwide manufacturer of specialty organic chemicals founded in 1946. TCI provides organic laboratory chemicals as well as pharmaceutical, cosmetic and functional materials. More than 70 years of synthesis experience and multi-purpose plants enable TCI to offer more than 30,000 products as well as custom synthesis.
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      Product(s):
      O0024 1,8-Octanediol >99.0%(GC)
       
Synonyms   Articles   Notes   Search
CAS Number: 629-41-4Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg: 211-090-8
FDA UNII: 806K32R50Z
Nikkaji Web: J96.516B
Beilstein Number: 1633499
MDL: MFCD00002989
XlogP3-AA: 1.40 (est)
Molecular Weight: 146.22986000
Formula: C8 H18 O2
NMR Predictor: Predict (works with chrome or firefox)
Category: plasticizers
 
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
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Physical Properties:
Assay: 95.00 to 100.00 % 
Food Chemicals Codex Listed: No
Melting Point: 63.00 °C. @ 760.00 mm Hg
Melting Point: 59.00 to  61.00 °C. @ 760.00 mm Hg
Boiling Point: 278.00 to  279.00 °C. @ 760.00 mm Hg (est)
Boiling Point: 171.00 to  173.00 °C. @ 20.00 mm Hg
Vapor Pressure: 0.001000 mmHg @ 25.00 °C. (est)
Flash Point: 230.00 °F. TCC ( 110.00 °C. )
logP (o/w): 0.970 (est)
Soluble in:
 alcohol
 water, 2538 mg/L @ 25 °C (est)
Insoluble in:
 water
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Organoleptic Properties:
 
Odor and/or flavor descriptions from others (if found).
 
 
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Cosmetic Information:
CosIng: cosmetic data
Cosmetic Uses: plasticisers
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Suppliers:
BOC Sciences
For experimental / research use only.
1,8-octanediol 96%
EMD Millipore
For experimental / research use only.
1,8-Octanediol
Jiangyin Healthway
1,8-Octanediol
New functional food ingredients
Matrix Scientific
For experimental / research use only.
1,8-Octanediol, 95+%
Santa Cruz Biotechnology
For experimental / research use only.
1,8-Octanediol
Sigma-Aldrich: Aldrich
For experimental / research use only.
1,8-Octanediol 98%
TCI AMERICA
For experimental / research use only.
1,8-Octanediol >99.0%(GC)
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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:
Not determined
Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
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Safety in Use Information:
Category: plasticizers
Recommendation for 1,8-octane diol usage levels up to:
 not for fragrance use.
 
Recommendation for 1,8-octane diol flavor usage levels up to:
 not for flavor use.
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Safety References:
EPI System: View
AIDS Citations: Search
Cancer Citations: Search
Toxicology Citations: Search
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 69420
National Institute of Allergy and Infectious Diseases: Data
WGK Germany: 3
 octane-1,8-diol
Chemidplus: 0000629414
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References:
 octane-1,8-diol
NIST Chemistry WebBook: Search Inchi
Pubchem (cid): 69420
Pubchem (sid): 135028468
Pherobase: View
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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
CHEMBL: View
KEGG (GenomeNet): C14218
HMDB (The Human Metabolome Database): Search
Export Tariff Code: 2905.39.9000
VCF-Online: VCF Volatile Compounds in Food
ChemSpider: View
Wikipedia: View
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Potential Blenders and core components note
 
None Found
 
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Potential Uses:
None Found
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Occurrence (nature, food, other): note
 malus micromalus makino
Search Trop  Picture
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Synonyms:
1,8-dihydroxyoctane
 octamethylene glycol
 octane-1,8-diol
1,8-octanediol
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Articles:
PubMed: First total synthesis of acetylenic alcohol 15-methyltricosa-2,4-diyne-1, 6-diol (strongylodiol-G) derived from marine sponge.
PubMed: Synthesis and characterization of poly(1,2-propanediol-co-1,8-octanediol-co-citrate) biodegradable elastomers for tissue engineering.
PubMed: Biodegradable polyesters containing ibuprofen and naproxen as pendant groups.
PubMed: Sustained, localized transgene expression mediated from lentivirus-loaded biodegradable polyester elastomers.
PubMed: Engaging stem cells for customized tendon regeneration.
PubMed: Identification and field evaluation of sex pheromone components of the pear barkminer moth, Spulerina astaurota.
PubMed: Synthesis of novel lidocaine-releasing poly(diol-co-citrate) elastomers by using deep eutectic solvents.
PubMed: Biosynthesis of unnatural bacteriochlorophyll c derivatives esterified with α,ω-diols in the green sulfur photosynthetic bacterium Chlorobaculum tepidum.
PubMed: Osteoblast biocompatibility on poly(octanediol citrate)/sebacate elastomers with controlled wettability.
PubMed: Urinary bladder smooth muscle regeneration utilizing bone marrow derived mesenchymal stem cell seeded elastomeric poly(1,8-octanediol-co-citrate) based thin films.
PubMed: Triterpenoid saponins and monoterpenoid glycosides from Incarvillea delavayi.
PubMed: Exploring chain length selectivity in HIC-catalyzed polycondensation reactions.
PubMed: Polyoctanediol citrate/sebacate bioelastomer films: surface morphology, chemistry and functionality.
PubMed: Synthesis and characterization of a biodegradable elastomer featuring a dual crosslinking mechanism.
PubMed: Two-step biocatalytic route to biobased functional polyesters from omega-carboxy fatty acids and diols.
PubMed: Comparison of two vectors for functional expression of a bacterial cytochrome P450 gene in Escherichia coli using CYP153 genes.
PubMed: Biodegradable nitric oxide-releasing poly(diol citrate) elastomers.
PubMed: Different alkyl dimethacrylate mediated stearyl methacrylate monoliths for improving separation efficiency of typical alkylbenzenes and proteins.
PubMed: Novel biodegradable poly(1,8-octanediol malate) for annulus fibrosus regeneration.
PubMed: Synthesis and characterization of branched polymers from lipase-catalyzed trimethylolpropane copolymerizations.
PubMed: Effects of porous polystyrene resin parameters on Candida antarctica lipase B adsorption, distribution, and polyester synthesis activity.
PubMed: In vitro characterization of a compliant biodegradable scaffold with a novel bioreactor system.
PubMed: Hemocompatibility evaluation of poly(diol citrate) in vitro for vascular tissue engineering.
PubMed: Effects of macroporous resin size on Candida antarctica lipase B adsorption, fraction of active molecules, and catalytic activity for polyester synthesis.
PubMed: Production of alpha, omega-alkanediols using Escherichia coli expressing a cytochrome P450 from Acinetobacter sp. OC4.
PubMed: Influence of PEG endgroup and molecular weight on its reactivity for lipase-catalyzed polyester synthesis.
PubMed: Synthesis and characterization of 3,13- and 2,13-octadecadienyl compounds for identification of the sex pheromone secreted by a clearwing moth, Nokona pernix.
PubMed: A new biodegradable polyester elastomer for cartilage tissue engineering.
PubMed: Synthesis of segmented poly(ether urethane)s and poly(ether urethane urea)s incorporating various side-chain or backbone functionalities.
PubMed: Dioxododecenoic acid: a lipid hydroperoxide-derived bifunctional electrophile responsible for etheno DNA adduct formation.
PubMed: Enzymatic synthesis of multi-component copolymers and their structural characterization.
PubMed: Simple synthesis of beta-D-glycopyranosides using beta-glycosidase from almonds.
PubMed: Crosslinked poly(methyl vinyl ether-co-maleic anhydride) as topical vehicles for hydrophilic and lipophilic drugs.
PubMed: Lipase-catalyzed polycondensations: effect of substrates and solvent on chain formation, dispersity, and end-group structure.
PubMed: Alcoholysis of Urea Catalyzed by Palladium(II) Complexes.
PubMed: Synthesis of a novel sialic acid derivative (sialylphospholipid) as an antirotaviral agent.
PubMed: Kinetics of pulmonary uptake of serotonin during exercise in dogs.
PubMed: Synthesis of neoglycoconjugates using oligosaccharide transferring activity of ceramide glycanase.
PubMed: DNA interstrand crosslinking and sequence selectivity of dimethanesulphonates.
PubMed: Use of norepinephrine uptake to measure lung capillary recruitment with exercise.
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