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Detail of > 533-50-6

  • MSDS Download
  • CAS Number:
  • 533-50-6
  • Name:
  • 2-Butanone,1,3,4-trihydroxy-, (3S)-

  • Superlist Name:
  • L-Erythrulose
  • Formula:
  • C4H8O4
  • Molecular Structure:
  • Synonyms:
  • 2-Butanone,1,3,4-trihydroxy-, (S)-;L-glycero-Tetrulose (7CI,8CI);L-Erythrulose;
  • Molecular Weight:
  • 120.10392
  • Density:
  • 1.42g/cm3
  • Boiling Point:
  • 349.6 °C at 760 mmHg
  • Flash Point:
  • 179.4 °C
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CAS No. 

533-50-6 L-Erythrulose

L-Erythrulose
Germany   412
  • Tel:+49-4101-3053-0
  • Address:Waldhofstrasse 14 ,25474 Ellerbek Germany

CAS No. 

533-50-6 L-Erythrulose

INCI Name (CTFA) : Erythrulose ELINCS No. : 443-800-9 HS CODE: 2914400090 The advantages of Erythrulose can only be fully realised when it is used solely and a product with the following advantages is desired: . Seldom cleavage products and considerably less skin irri
China (Mainland)   4
  • Tel:+86-25-86620042
  • Address:40 Ma Jia Jie

CAS No. 

533-50-6 L-Erythrulose

Tanning agent
United States  
  • Tel:203-822-9800
  • Address:20 Glover Ave., Norwalk, CT, 06850, USA

CAS No. 

533-50-6 L-Erythrulose

Erythrulose
Switzerland  
  • Tel:41 61 706 4848
  • Address:Engelgasse 109, 4002 Basel, Switzerland
  • Total:4 Page 1 of 1 1
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    Reference

    In situ product removal from E
    In situ product removal from E. coli transketolase-catalyzed biotransformations. Chauhan, Rashmi P.; Woodley, John M.; Powell, Lawson W. ( Advanced Center for Biochemical Engineering, Department of Chemical and Biochemical Engineering, University College London, London WC1E 7JE, UK). Annals of the New York Academy of Sciences, 799(Enzyme Engineering XIII), 545-554 (English) 1996 New York Academy of Sciences. CODEN: ANYAA9. ISSN: 0077-8923. DOCUMENT TYPE: Journal; General Review CA Section: 10 (Microbial, Algal, and Fungal Biochemistry) Section cross-reference(s): 7 A review, with 33 refs., describing studies conducted to establish a recovery method for the product of a model E. 9014-48-6 and 533-50-6 which are cas registry numbers of substances are two of reagents here. coli transketolase-catalyzed biotransformation. The philosophy behind using in situ product removal is also addressed and discussed with regard to formulating a rational approach to product recovery from biotransformations. .
    Separation of trioses and tetroses as trimethylsilyl oximes by gas chromatography
    Separation of trioses and tetroses as trimethylsilyl oximes by gas chromatography. Anderle, Dusan; Konigstein, Jozef; Kovacik, Vladimir (Inst. Chem., Slovak Acad. Sci., Bratislava, Czech.). Anal. Chem., 49(1), 137-9 (English) 1977. CODEN: ANCHAM. DOCUMENT TYPE: Journal CA Section: 80 (Organic Analytical Chemistry) Tetroses were sepd. by gas chromatog. of their per-O-Me3Si oximes on a capillary column coated with OV-17. Trioses could be satisfactorily sepd. on a packed column with SP-2340 as a stationary phase. The achieved resoln. R .gtoreq. 1 fulfills criteria required for quant.In this experiment, several chemicals are used like 533-50-6 and 61520-35-2 anal. Mass spectra of the derivs. are also presented. .

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