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Surfactant intermediate 3-Chloro-2-hydroxypropane-1-sulfonic acid sodium salt 126-83-0

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  • 126-83-0| Sodium 3-chloro-2-hydroxypropane-1

    Its name is 3-chloro-2-hydroxypropane-1-sulfonic acid Chemsrc provides CAS#:107-57-3 MSDS, density, melting point, boiling point, structure, etc. CAS Number Search

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  • 3-CHLORO-2-HYDROXYPROPANESULFONIC ACID

    3-Hydroxypropane-1-sulfonic acid technical, ~80% (T) CAS Number 15909-83-8. Linear Formula HOCH 2 CH 2 CH 2 SO 3 H . Molecular Weight 140.16 . Beilstein/REAXYS Number 1753832 . MDL number MFCD00066499. PubChem Substance ID 57651575. NACRES NA.22

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    Synonym: 4-Chloro-7-sulfobenz-2-oxa-1,3-diazole ammonium salt, 7-Chloro-2,1,3-benzoxadiazole-4-sulfonic acid ammonium salt, 7-Chloro-4-benzofurazansulfonic acid ammonium salt, SBF-Chloride Linear Formula: C 6 H 3 ClN 2 O 4 S · NH 3

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    Synonym: 2,2′-{[(2-Hydroxypropane-1,3-diyl)bis(oxy)]bis(4,1-phenylene)}diacetamide Empirical Formula (Hill Notation): C 19 H 22 N 2 O 5 Molecular Weight: 358.39

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    Synonym: 1,2-Naphthoquinone-4-sulfonic acid sodium salt, 3,4-Dihydro-3,4-dioxo-1-naphthalenesulfonic acid sodium salt, Folin’s reagent Empirical Formula (Hill Notation): C …

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  • Anthraquinone-2-sulfonic acid, sodium salt

    Synonym: 9,10-Dihydro-9,10-dioxo-2-anthracenesulfonic acid sodium salt monohydrate, Sodium anthraquinone-2-sulfonate Empirical Formula (Hill Notation): C 14 H 7 NaO 5 S · H 2 …

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    2001-1-1 · This chapter discusses the chemistry of surfactants. Surface active substances or surfactants are amphiphilic compounds having a lyophilic, in particular hydrophilic, part (polar group) and a lyophobic, in particular hydrophobic, part (often hydrocarbon chain).

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  • US6320080B2 - Branched surfactant manufacture -

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    A method and composition for controlling corrosion of metals, particularly ferrous-based metals in contact with aqueous systems is disclosed, which includes treating industrial waters with a combination of a tetrazolium salt of the general formula: where R1, R2 and R3 may be various organic or inorganic substitutents, where n may be 1 or 2, and at least one other aqueous system treatment material.

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    2020-4-6 · trisodium 4-chloro-5-methyl-1H-1,2,3-benzotriazol-1-ide 4-chloro-7-methyl-1H-1,2,3-benzotriazol-1-ide 5-chloro-4-methyl-1H-1,2,3-benzotriazol-1-ide 03226f1f-3fcf-4b48-b54c-c2bfd27efa36 Hydrocarbons, C5-11, nonaroms.-rich, reforming light fraction [A complex combination of hydrocarbons obtained by separation from the platformate-containing fraction.

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    2019-5-25 · Chiral Chemical Synthesis of DNA Containing (S)-9-(1,3-Dihydroxy-2-propoxymethyl)guanine (DHPG) and Effects on Thermal Stability, Duplex Structure, and Thermodynamics of Duplex Formation. Biochemistry 1995, 34 (28) , 9235-9248. DOI: 10.1021/bi00028a037.

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    2-Propenoic acid, telomers with Bu alc.-2-[(2-propen-1-yloxy)methyl]oxirane reaction products, sodium bisulfite andsodium 2-hydroxy-3-(2-propen-1-yloxy)-1-propanesulfonate (1:1), sodium salts, peroxydisulfuric acid([(HO)S(O)2]2O2) sodium salt (1:2)-initiated P-18-0100

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  • 3-CHLORO-2-HYDROXYPROPANESULFONIC ACID

    3-CHLORO-2-HYDROXYPROPANESULFONIC ACID SODIUM SALT CAS 126-83-0, US 8 - 20 Kilogram, 126-83-0, 126-83-0, CHPS-Na, C3H6O4ClSNa.Source from Wuhan Dongxin Mill Imp&Exp Trade Co., Ltd. on hotelpentagone.com.

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    Product Application. As there are halogen atoms and Hydroxy with strong activity ,and aslo sulfonate group with Hydrophilic In the molecular instruction of 3-Chloro-2-hydroxypropanesulfonic acid, sodium salt , CHPS-Na is an important functional monomer in the field of synthesizing spolymer industry and it is aslo an organic chemical intermediate which is used in the preparation of Surfactant ...

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  • The Structure of Zwitterionic Phosphocholine

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  • Subject Index - ScienceDirect

    1992-1-1 · 555 Subject Index absolute mobilities 332 absorbing analytes 91 absorbing co-ion 124 absorption 397 absorptivity 66 accelerators 491, 496, 529 acenaphtene 477 N-(2-acetaiiiido)-2-aminoethanesulfonic acid (ACES) 206 acetaminophen 440, 441 acetate 48, 207, 209, 463 acetic acid 478, 479 acetonilrile 219 acetophenone 472, 476 2,3,4,6-tetra-0-acetyl-y8-D-glucopyranosyl iso- …

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  • US Patent for Method and composition for inhibiting ...

    A method and composition for controlling corrosion of metals, particularly ferrous-based metals in contact with aqueous systems is disclosed, which includes treating industrial waters with a combination of a tetrazolium salt of the general formula: where R1, R2 and R3 may be various organic or inorganic substitutents, where n may be 1 or 2, and at least one other aqueous system treatment material.

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  • A review on semi-aromatic polyamide TFC

    2017-6-30 · Typical formulation used by Sasaki contained 1% of PIP, 0.2% of 1,3-bis-(4-piperidyl)propane, 0.5% of sodium dodecyl sulfate, and 1% of trisodium phosphate by weight , . The substrate was coated with a 1% (w/v) solution formed by dissolving a mixture of IPC/TMC (weight ratio = 2/1) in trichlorotrifluoroethane.

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    Typical Properties AppearanceWhite crystal power Purity (%)98.5% Density (g/cm3)1.649g/cm3 Boiling point (℃)N CAS No.126-83-0 Melting pointN71-72 Mol. wt. MF Flashing point196.6 C3H6O4ClSNa 148.8 APPLICATION -The molecular structure of sodium 3-chloro-2-hydroxypropane sulfonate contains both a highly active halogen atom and a hydroxyl group, as well as a hydrophilic sulfonate group.

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    2012-12-4 · The most common product has a carbon num- ber range of the alkyl chain from C 1 0 to C 1 3 (Scheme 1). The phenyl isomer distribution occurring therein is determined by the choice of catalyst. With use of AlCl 3, the content of 2-phenyl isomers is approximately 30% in mixture with 3-, 4-, 5-, and other phenyl isomers. In products of HF ...

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    2014-4-27 · Sucrose 130,000,000 0.70–0.80 The problem in manufacturing sucrose esters is re-Glucose 16,000,000 0.55–1.12 lated to the high functionality of the sucrose molecule Sorbitol 8,000,000 0.53–1.70 with eight hydroxyl groups, which compete during the a Private communication (Cerestar, Henkel). derivatization step (Fig. 20).

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  • US Patent for No-releasing nitrooxy-chromene

    The present invention provides NO-releasing nitrooxy-alkylenyl-linked-chromene conjugates, having the structure of Formula (1) wherein R1, R2, R3, R4, X, and L are as defined in the detailed description; pharmaceutical compositions comprising at least one compound o Formula (I); and methods useful for healing wounds, preventing and treating cancer and treating actinic keratosis, cystic ...

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    2021-3-4 · However, when 1 was treated with Li+, Mn2+, Fe2+, Co2+, and Zn2+, further titration experiments revealed that these metal ions coordinated via the lone pairs on the coordinating oxygen atoms of the F(4)Cat(2-) moieties in a one-to-one ratio, and binding

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  • 142126378 85190748-handbook-of-detergents-part-f

    Sodium sulfite is reacted with epichlorohydrin in water to produce a solution of 1-chloro-2-hydroxypropane sulfonate, which is further reacted with a tertiary amine to yield a quaternary ammonium group linked to the hydroxy- propane sulfonate, with sodium chloride as the primary by-product.

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  • Phosphoinositide3-kinase inhibiting compounds and

    FIELD: chemistry. SUBSTANCE: invention relates to compounds of formulae Ic-d , where X is O or S; R 1 is selected from -(CR 14 R 15) n NR 12 C(=Y)R 10, -(CR 14 R 15) n NR 12 S(O) 2 R 10, -(CR 14 R 15) n OR 10, -C(=Y)NR 10 R n, -C(-O)NR 12 (CR 14 R 15) m NR 10 R H, -NHR 12, C 1-C 12 alkyl, C 2-C 8 alkenyl, C 3-C 6 heterocyclyl, which is a saturated carboxylic radical containing 3-6 ring atoms ...

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    1-(2-Naphtholazo-3,6-disulfonic acid)-2-Naphthol-4-sulfonic acid, disodium salt H2NOH•HCl(aq) Hydroxylamine hydrochloride solution, aqueous Acid blue 74; C.I. 73015; Indigocarmine Iron (II) ammonium sulfate solution, aqueous Iron (III) nitrate solution, aqueous Cor/Car/T/OX 4 E Protective Eyewear Codes HMIS Labeling System 3 E 3 H

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  • Solutions Manual for chemist 2 | Cracking (Chemistry ...

    2015-7-26 · Review exercise 5.3 1 After 1st 2.6 hours: 0.1/2 = 0.05 g After 5.2 hours: 0.025 g After 7.8 hours: 0.0125 g 2 1st half-life: 0.120/2 = 0.06 g 2nd half-life: 0.06/2 = 0.03 g Solutions Manual: Module 1 Production of materials Pearson Education Australia (a division of Pearson Australia Group Pty Ltd) 2006.

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