110-63-4

  • Product Name:1,4-Butanediol
  • Molecular Formula:C4H10O2
  • Purity:99%
  • Molecular Weight:
Inquiry

Product Details;

CasNo: 110-63-4

Molecular Formula: C4H10O2

Appearance: viscous colourless liquid

110-63-4 Properties

  • Molecular Formula:C4H10O2
  • Molecular Weight:90.1222
  • Appearance/Colour:viscous colourless liquid 
  • Vapor Pressure:0.015mmHg at 25°C 
  • Melting Point:20 °C 
  • Refractive Index:n20/D 1.445(lit.)  
  • Boiling Point:227.999 °C at 760 mmHg 
  • PKA:14.73±0.10(Predicted) 
  • Flash Point:105.909 °C 
  • PSA:40.46000 
  • Density:1.006 g/cm3 
  • LogP:-0.24880 

110-63-4 Usage

InChI:InChI=1/C4H10O2/c5-3-1-2-4-6/h5-6H,1-4H2

110-63-4 Relevant articles

Effect of boron content on 1,4-butanediol production by hydrogenation of succinic acid over Re-Ru/BMC (boron-modified mesoporous carbon) catalysts

Kang, Ki Hyuk,Han, Seung Ju,Lee, Jong Won,Kim, Tae Hyeop,Song, In Kyu

, p. 206 - 213 (2016)

Hydrogenation of γ-Butyrolactone to 1,4-Butanediol over CuCo/TiO2 Bimetallic Catalysts

Huang, Zhiwei,Barnett, Kevin J.,Chada, Joseph P.,Brentzel, Zachary J.,Xu, Zhuoran,Dumesic, James A.,Huber, George W.

, p. 8429 - 8440 (2017)

Extremely facile and selective nickel-catalyzed allyl ether cleavage

Taniguchi, Takahiko,Ogasawara, Kunio

, p. 1136 - 1137 (1998)

Thermodynamic equilibria between polyalcohols and cyclic ethers in high-temperature liquid water

Yamaguchi, Aritomo,Hiyoshi, Norihito,Sato, Osamu,Bando, Kyoko K.,Masuda, Yoshio,Shirai, Masayuki

, p. 2666 - 2668 (2009)

 

A temperature-controlled reversible ionic liquid - Water two phase - Single phase protocol for hydrogenation catalysis

Dyson,Ellis,Welton

, p. 705 - 708 (2001)

Comparison of Carbon-13 Nuclear Magnetic Resonance Methods for the Analysis of Multiple Partially Deuteriated Products from Catalytic Reactions: Heptan-1-ol and 2-Methylpropanol

MacDougall, Joanna K.,Simpson, Michael C.,Cole-Hamilton, David J.

, p. 3061 - 3066 (1994)

A Study of the Catalytic Deuteration of 1,4-Butynediol

Chickos, James S.,Uang, Jack Y.-J.,Keiderling, Tim A.

, p. 2594 - 2596 (1991)

High chemo and regioselective formation of alcohols from the hydrocarbonylation of alkenes using cooperative ligand effects

Boogaerts, Ine T.I. F.,White, Daniel F. S.,Cole-Hamilton, David J.

, p. 2194 - 2196 (2010)

Continuous hydrogenation of 2-butyne-1,4-diol to 2-butene- and butane-1,4-diols

Rode,Tayade,Nadgeri,Jaganathan,Chaudhari

, p. 278 - 284 (2006)

A new carboxylesterase from Brevibacterium linens IFO 12171 responsible for the conversion of 1,4-butanediol diacrylate to 4-hydroxybutyl acrylate: Purification, characterization, gene cloning, and gene expression in Escherichia coli

Sakai, Yasuyoshi,Ishikawa, Junko,Fukasaka, Shunji,Yurimoto, Hiroya,Mitsui, Ryoji,Yanase, Hideshi,Kato, Nobuo

, p. 688 - 697 (1999)

Effect of Ethers on Reactions of Butylcoppers with α,β-Unsaturated Ketones in Toluene

Kingsbury, Celia L.,Smith, Robin A. J.

, p. 7637 - 7643 (1997)

A Novel and Unusual Reaction of Enol Ethers with Benzyltriethylammonium Borohydride and Chlorotrimethylsilane

Baskaran, S.,Chidambaram, N.,Narasimhan, N.,Chandrasekaran, S.

, p. 6371 - 6374 (1992)

A Schiff Base Modified Pd Catalyst for Selective Hydrogenation of 2-Butyne-1,4-diol to 2-Butene-1,4-diol

Li, Haomeng,Wang, Xinkui,Chen, Xiao,Li, Chuang,Wang, Min,Yi, Yanhui,Ji, Min,Wang, Huilong,Shao, Zhengfeng,Liang, Changhai

, p. 2150 - 2157 (2020)

Bimetallic Synergy Effects of Phyllosilicate-Derived NiCu@SiO2 Catalysts for 1,4-Butynediol Direct Hydrogenation to 1,4-Butanediol

Wang, Changzhen,Tian, Yani,Wu, Ruifang,Li, Haitao,Yao, Benzhen,Zhao, Yongxiang,Xiao, Tiancun

, p. 4777 - 4787 (2019)

Quantification of Interfacial pH Variation at Molecular Length Scales Using a Concurrent Non-Faradaic Reaction

Ryu, Jaeyune,Wuttig, Anna,Surendranath, Yogesh

, p. 9300 - 9304 (2018)

Modelling proposed intermediates in the hydrocarbonylation of alkenes catalysed by rhodium complexes of PBui3 and PPr i3

Cheliatsidou, Paraskevi,White, Daniel F. S.,Slawin, Alexandra M. Z.,Cole-Hamilton, David J.

, p. 2389 - 2394 (2008)

DIRECT SYNTHESIS OF 1,4-BUTANEDIOL FROM ALLYL ALCOHOL USING CARBON MONOXIDE AND WATER IN THE PRESENCE OF Rh6(CO)16-PROPANEDIAMINE SYSTEM

Kaneda, Kiyotomi,Imanaka, Toshinobu,Teranishi, Shiichiro

, p. 1465 - 1466 (1983)

An unusual reaction of cyclic enol ethers with titanium(III) tetrahydroborate

Ravikumar,Chandrasekaran, Srinivasan

, p. 2973 - 2978 (1997)

Alkaline hydrolysis of oligomers of tartrate esters: Effect of a neighboring carboxyl on the reactivity of ester groups

Maniar,Kalonia,Simonelli

, p. 705 - 709 (1992)

New environmentally friendly catalysts containing Pd-interstitial carbon made from Pd-glucose precursors for ultraselective hydrogenations in the liquid phase

Chan, Chun Wong Aaron,Xie, Yaling,Cailuo, Nick,Yu, Kai Man Kerry,Cookson, James,Bishop, Peter,Tsang, Shik Chi

, p. 7971 - 7973 (2011)

Zirconium(IV) chloride catalyzed new and efficient protocol for the selective cleavage of p-methoxybenzyl ethers

Madhava Sharma, Gangavaram V.,Reddy, Ch. Govardhan,Krishna, Palakodety Radha

, p. 4574 - 4575 (2003)

Efficient Pd@MIL-101(Cr) hetero-catalysts for 2-butyne-1,4-diol hydrogenation exhibiting high selectivity

Yin, Dongdong,Li, Chuang,Ren, Hangxing,Shekhah, Osama,Liu, Jinxuan,Liang, Changhai

, p. 1626 - 1633 (2017)

Aqueous phase hydrogenation of acetic acid to ethanol over Ir-MoO x/SiO2 catalyst

Wang, Zhiqiang,Li, Guangyi,Liu, Xiaoyan,Huang, Yanqiang,Wang, Aiqin,Chu, Wei,Wang, Xiaodong,Li, Ning

, p. 38 - 41 (2014)

Raney Ni-Si catalysts for selective hydrogenation of highly concentrated 2-butyne-1,4-diol to 2-butene-1,4-diol

Chen, Xiao,Zhang, Mingming,Yang, Kaixuan,Williams, Christopher T.,Liang, Changhai

, p. 1118 - 1126 (2014)

Kinetics and mechanism of tetrahydrofuran synthesis via 1,4-butanediol dehydration in high-temperature water

Hunter, Shawn E.,Ehrenberger, Carolyn E.,Savage, Phillip E.

, p. 6229 - 6239 (2006)

Liquid-phase catalytic hydrogenation of 2-butyne-1,4-diol to 1,4-butanediol at atmospheric pressure on suspended catalysts

Pyatnitsyna,El'Chaninov

, p. 394 - 397 (2013)

Analysis of drugs by pyrolysis. I. Selected ion monitoring combined with a pyrolysis method for the determination of carpronium chloride in biological samples.

Ohya,Sano

, p. 241 - 247 (1977)

Selective Hydrogenation of Cyclic Ester to α,ω-Diol Catalyzed by Cationic Ruthenium Complexes with Trialkylphosphine Ligands

Hara, Yoshinori,Inagaki, Hiroko,Nishimura, Sugio,Wada, Keisuke

, p. 1983 - 1986 (1992)

Tracking Electrical Fields at the Pt/H2O Interface during Hydrogen Catalysis

Ryu, Jaeyune,Surendranath, Yogesh

, p. AR (2019)

First example of borirane synthesis by α-olefins reaction with BCl3·SMe2 Catalyzed with (η5-C5H5)2TiCl2

Khusainova,Khafizova,Tyumkina,Dzhemilev

, p. 1517 - 1523 (2015)

Converging conversion - using promiscuous biocatalysts for the cell-free synthesis of chemicals from heterogeneous biomass

Pick, André,Sieber, Volker,Sutiono, Samuel

, p. 3656 - 3663 (2021)

Catalytic hydrogenation of 2-butyne-1,4-diol to 2-butene-1,4-diol at atmospheric pressure in the liquid phase

Pyatnitsyna,El'chaninov,Savost'yanov

, p. 89 - 92 (2006)

Hydroboration Reaction and Mechanism of Carboxylic Acids using NaNH2(BH3)2, a Hydroboration Reagent with Reducing Capability between NaBH4and LiAlH4

Wang, Jin,Ju, Ming-Yue,Wang, Xinghua,Ma, Yan-Na,Wei, Donghui,Chen, Xuenian

, p. 5305 - 5316 (2021/04/12)

110-63-4 Process route

C<sub>36</sub>H<sub>60</sub>O<sub>30</sub>*C<sub>4</sub>H<sub>10</sub>O<sub>2</sub>

C36H60O30*C4H10O2

Butane-1,4-diol
110-63-4

Butane-1,4-diol

alpha cyclodextrin
10016-20-3

alpha cyclodextrin

Conditions
Conditions Yield
In water; at 25 ℃; Equilibrium constant;
 
dimethyl cis-but-2-ene-1,4-dioate
624-48-6

dimethyl cis-but-2-ene-1,4-dioate

tetrahydrofuran
109-99-9,24979-97-3,77392-70-2

tetrahydrofuran

2-methoxytetrahydrofuran
13436-45-8

2-methoxytetrahydrofuran

4-butanolide
96-48-0

4-butanolide

propan-1-ol
71-23-8

propan-1-ol

1-methoxy-1,4-butanediol

1-methoxy-1,4-butanediol

2-(4'-hydroxybutoxy)-tetrahydrofuran
64001-06-5

2-(4'-hydroxybutoxy)-tetrahydrofuran

4-hydroxy-butanoic acid 4-hydroxybutyl ester

4-hydroxy-butanoic acid 4-hydroxybutyl ester

Butane-1,4-diol
110-63-4

Butane-1,4-diol

4-hydroxybutyraldehyde
25714-71-0

4-hydroxybutyraldehyde

methyl 4-hydroxybutanoate
925-57-5

methyl 4-hydroxybutanoate

butan-1-ol
71-36-3

butan-1-ol

Conditions
Conditions Yield
With hydrogen; at 190 ℃; under 46504.7 Torr; Gas phase;
79.1%
10.4%
5.3%

110-63-4 Upstream products

  • 1708-29-8
    1708-29-8

    2,5-dihydrofuran

  • 108-31-6
    108-31-6

    maleic anhydride

  • 110-52-1
    110-52-1

    1,4-dibromo-butane

  • 110-65-6
    110-65-6

    1,4-dihydroxybut-2-yne

110-63-4 Downstream products

  • 13179-96-9
    13179-96-9

    1,4-dimethoxybutane

  • 5835-79-0
    5835-79-0

    4-(1-hydroxypropyl)morpholine

  • 53161-64-1
    53161-64-1

    4,4'-butane-1,4-diyl-bis-morpholine

  • 7191-20-0
    7191-20-0

    2-phenyl-1,3,2-dioxaphosphepin-2-oxide