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1,3-Dichloro-2-propanol - 98%, high purity , CAS No.96-23-1
Basic Description
Synonyms
EINECS 247-787-9 | FT-0606643 | NSC 70982 | UN 2750 | DTXSID6025010 | HSDB 5302 | Gdch | J-503895 | Q10843705 | 1,3-Dichloroisopropyl alcohol | NCGC00091689-01 | NCGC00091689-03 | NSC70982 | NSC-70982 | CCRIS 953 | 1,3-DICHLORO-2-PROPANOL [IARC] | NCGC002
Specifications & Purity
≥98%
Storage Temp
Argon charged
Shipped In
Normal
Product Description
1,3-Dichloro-2-propanol is a food processing contaminant. Biotransformation of 1,3-dichloro-2-propanol to epichlorohydrin by the whole cells of recombinant Escherichia coli via resin-based in situ product removal has been investigated.
Taxonomic Classification
Kingdom
Organic compounds
Superclass
Organohalogen compounds
Class
Halohydrins
Subclass
Chlorohydrins
Intermediate Tree Nodes
Not available
Direct Parent
Chlorohydrins
Alternative Parents
Secondary alcohols Organochlorides Hydrocarbon derivatives Alkyl chlorides
Molecular Framework
Aliphatic acyclic compounds
Substituents
Secondary alcohol - Chlorohydrin - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Organochloride - Alkyl halide - Alkyl chloride - Alcohol - Aliphatic acyclic compound
Description
This compound belongs to the class of organic compounds known as chlorohydrins. These are alcohols substituted by a chlorine atom at a saturated carbon atom otherwise bearing only hydrogen or hydrocarbyl groups.
External Descriptors
secondary alcohol - organochlorine compound
Data sources
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
Associated Targets(Human)
Mechanisms of Action
Mechanism of Action
Action Type
target ID
Target Name
Target Type
Target Organism
Binding Site Name
References
Names and Identifiers
Pubchem Sid
488180371
Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/488180371
IUPAC Name
1,3-dichloropropan-2-ol
INCHI
InChI=1S/C3H6Cl2O/c4-1-3(6)2-5/h3,6H,1-2H2
InChIKey
DEWLEGDTCGBNGU-UHFFFAOYSA-N
Smiles
C(C(CCl)O)Cl
Isomeric SMILES
C(C(CCl)O)Cl
WGK Germany
3
RTECS
UB1400000
UN Number
2750
Packing Group
II
Molecular Weight
128.99
Beilstein
1732063
Reaxy-Rn
1732063
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1732063&ln=
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
Chemical and Physical Properties
Solubility
Fully miscible in water.
Sensitivity
air sensitive
Refractive Index
1.4802
Flash Point(°C)
85℃
Boil Point(°C)
174°C
Melt Point(°C)
-4°C
Molecular Weight
128.979 g/mol
XLogP3
0.800
Hydrogen Bond Donor Count
1
Hydrogen Bond Acceptor Count
1
Rotatable Bond Count
2
Exact Mass
127.98 Da
Monoisotopic Mass
127.98 Da
Topological Polar Surface Area
20.200 Ų
Heavy Atom Count
6
Formal Charge
0
Complexity
28.000
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
The total count of all stereochemical bonds
0
Covalently-Bonded Unit Count
1
Citations of This Product
1.
Jianxia Sun,Shun Bai,Weibin Bai,Feiyan Zou,Lei Zhang,Guoqiang Li,Yunfeng Hu,Mingwei Li,Rian Yan,Zhijian Su,Yadong Huang.
(2014-02-13)
1,3-Dichloro-2-propanol inhibits progesterone production through the expression of steroidogenic enzymes and cAMP concentration in Leydig cells..
Food chemistry,
154
(330-336).
2.
Yuqi Zhang, Jiasi Yan, Rixin You, Meng He, Ligen Wang, Minghui Liang.
(2023)
The effect of the interaction between Cu single atoms and Pt nanoparticles on the selective hydrogenation of epichlorohydrin to chloro-propanol.
APPLIED SURFACE SCIENCE,
628
(157382).
3.
Yuchen Du, Yuan Guo, Xuan Xiao, Xiaonan Zhu, Ye Liu, Xiuhang Ruan, Xiaofei Huang, Youyong Yuan, Xinhua Wei.
(2022)
Glutathione depletion and photosensitizer activation augments efficacy of tumor photodynamic immunotherapy.
CHEMICAL ENGINEERING JOURNAL,
442
(136170).
4.
Shiwei Luo, Di Ma, Ruili Wei, Wang Yao, Xinrui Pang, Ye Wang, Xiangdong Xu, Xinhua Wei, Yuan Guo, Xinqing Jiang, Youyong Yuan, Ruimeng Yang.
(2022)
A tumor microenvironment responsive nanoplatform with oxidative stress amplification for effective MRI-based visual tumor ferroptosis.
Acta Biomaterialia,
138
(518).
5.
Di Ma, Qingyu Zong, Yuchen Du, Fangzhou Yu, Xuan Xiao, Rong Sun, Yuan Guo, Xinhua Wei, Youyong Yuan.
(2021)
Sequential enzyme-activated macrotheranostic probe for selective tumor mitochondria targeting.
Acta Biomaterialia,
135
(628).
6.
Zhiyong Song, Huajuan Wang, Yang Wu, Jiangjiang Gu, Shuojun Li, Heyou Han.
(2018)
Fabrication of Bis-Quaternary Ammonium Salt as an Efficient Bactericidal Weapon Against Escherichia coli and Staphylococcus aureus.
ACS Omega,
3
(10):
(14517–14525).
7.
Xiuzhen Qiu, Xian-Yan Xu, Yong Liang, Huishi Guo.
(2018)
The molecularly imprinted polymer supported by anodic alumina oxide nanotubes membrane for efficient recognition of chloropropanols in vegetable oils.
FOOD CHEMISTRY,
258
(295).
8.
Jincheng Mao, Heng Zhang, Wenlong Zhang, Jinming Fan, Chong Zhang, Jinzhou Zhao.
(2018)
Dissymmetric beauty: A novel design of heterogemini viscoelastic surfactant for the clean fracturing fluid.
JOURNAL OF INDUSTRIAL AND ENGINEERING CHEMISTRY,
60
(133).
9.
Hongbin Ju, Lizhi Zhang, Heqin Guo, Litao Jia, Bo Hou, Debao Li, Tao Geng.
(2024)
Design of Organic–Inorganic Phase Transfer Hybrid Catalyst and Its Application in the Epoxidation of α-Olefins.
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH,
63
(18):
(8089-8101).
10.
Linlin Bian, Xue Ge, Senwei Feng, Guangxuan Chen, Kefeng Li, Xu Wang.
(2024)
Determination of chloropropanol esters and glycidyl esters in instant noodles based on solid-phase microextraction with chitosan-β-cyclodextrin coated fiber.
FOOD CHEMISTRY,
442
(138419).
11.
Hong-Bin Ju, Li-Zhi Zhang, De-Bao Li, Tao Geng, Ya-Jie Jiang, Ya-Kui Wang.
(2024)
The influence of hydrogen bonding on the structure of organic–inorganic hybrid catalysts and its application in the solvent-free epoxidation of α-olefins.
RSC Advances,
14
(18):
(12853-12863).
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