Dayang Chem (Hangzhou) Co., Ltd.
China
Product Name: N-ACETYL-L-SERINE
Price: $Inquiry/100g $Inquiry/1kg $Inquiry/100kg $Inquiry/1000kg
Purity: 98.0%
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16354-58-8

16354-58-8 structure

Name: acetylserine
Chemical Name: N-acetyl-L-serine
CAS Number: 16354-58-8
Molecular Formula: C₅H₉NO₄
Molecular Weight: 147.13
Catalog: Research Areas Others
Create Date: 2018-02-15 08:00:00
Modify Date: 2024-01-05 22:07:59
N-Acetylserine (N-Acetyl-L-serine) can bind to CysB apoprotein. N-acetylserine is the physiological inducer of cysteine biosynthesis. N-Acetylserine can stimulate in vitro cysJIH transcription[1][2].

Name	N-acetyl-L-serine
Synonyms	N-Acetyl-L-serin L-Serine, N-acetyl- Serine, N-acetyl-, DL- Serine, N-acetyl-, L- N-ACETYL-DL-SERINE L-Serine,N-acetyl N-Acetylserine acetylserine N-Acetyl-L-serine Serine, N-acetyl- (2S)-2-acetamido-3-hydroxypropanoic acid

Description	N-Acetylserine (N-Acetyl-L-serine) can bind to CysB apoprotein. N-acetylserine is the physiological inducer of cysteine biosynthesis. N-Acetylserine can stimulate in vitro cysJIH transcription[1][2].
Related Catalog	Research Areas >> Others
References	[1]. Lynch AS, et al. Characterization of the CysB protein of Klebsiella aerogenes: direct evidence that N-acetylserine rather than O-acetylserine serves as the inducer of the cysteine regulon. Biochem J. 1994 Apr 1;299 ( Pt 1)(Pt 1):129-36. [2]. Ostrowski J, et al. Molecular characterization of the cysJIH promoters of Salmonella typhimurium and Escherichia coli: regulation by cysB protein and N-acetyl-L-serine. J Bacteriol. 1989 Jan;171(1):130-40.

Density	1.3±0.1 g/cm3
Boiling Point	468.4±40.0 °C at 760 mmHg
Melting Point	207.6°C (lit.)
Molecular Formula	C₅H₉NO₄
Molecular Weight	147.13
Flash Point	237.1±27.3 °C
Exact Mass	147.053162
PSA	86.63000
LogP	-1.89
Vapour Pressure	0.0±2.6 mmHg at 25°C
Index of Refraction	1.494

HS Code	2924199090

56-45-1

108-24-7

~83%

16354-58-8

Literature: Zheng, Yan; Duanmu, Chuansong; Gao, Yong Organic Letters, 2006 , vol. 8, # 15 p. 3215 - 3217

5680-80-8

64-19-7

16354-58-8

Literature: FUJISAWA PHARMACEUTICAL CO., LTD. Patent: WO2004/111041 A1, 2004 ; Location in patent: Page 49-50 ; WO 2004/111041 A1

2311-26-4

16354-58-8

Literature: CARLSON, Erin E.; TRADER, Darci Patent: US2014/107328 A1, 2014 ; Location in patent: Paragraph 0081-0082 ;

5680-80-8

75-36-5

16354-58-8

Literature: American Cyanamid Company Patent: US4640913 A1, 1987 ;

114118-71-7

617-65-2

16354-58-8

Literature: Harada, Setsuo; Tsubotani, Shigetoshi; Hida, Tsuneaki; Ono, Hideo; Okazaki, Hisayoshi Tetrahedron Letters, 1986 , vol. 27, # 51 p. 6229 - 6232

5147-00-2

16354-58-8

Literature: Caswell, Michael; Chaturvedi, Rama K.; Lane, Stuart M.; Zvilichovsky, Bina; Schmir, Gaston L. Journal of Organic Chemistry, 1981 , vol. 46, # 8 p. 1585 - 1593

56-45-1

108-24-7

16354-58-8

2233-54-7

Literature: Mukai, Shin; Flematti, Gavin R.; Byrne, Lindsay T.; Besant, Paul G.; Attwood, Paul V.; Piggott, Matthew J. Amino Acids, 2012 , vol. 43, # 2 p. 857 - 874

56-23-5

56-45-1

108-24-7

16354-58-8

Literature: Akabori et al. Archives of Biochemistry, 1959 , vol. 83, p. 1,2

Precursor 9
56-45-1 108-24-7 5680-80-8 64-19-7
2311-26-4 75-36-5 114118-71-7 5147-00-2
56-23-5
DownStream 2
2311-26-4 56-45-1

HS Code	2924199090
Summary	2924199090. other acyclic amides (including acyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

16354-58-8	97-14-3
4985-36-8	152612-69-6
5147-00-2	2230887-17-7
25248-96-8	54322-41-7
2311-26-4	196601-67-9