L-Sulforaphane

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Names

[ CAS No. ]:
142825-10-3

[ Name ]:
L-Sulforaphane

[Synonym ]:
UNII:41684WL1GL
1-Isothiocyanato-4-(methylsulfinyl)butane
SULFORAPHANE, (±)-
4-Isothiocyanatobutyl methyl sulfoxide
4-Methylsulfinylbutyl isothiocyanate
1-Isothiocyanato-4-[(R)-methylsulfinyl]butane
4-(Methylsulfinyl)butyl isothiocyanate
Butane, 1-isothiocyanato-4-[(R)-(1R)-methylsulfinyl]-
Butane, 1-isothiocyanato-4-(methylsulfinyl)-
(R)-sulforaphane
MFCD09039283
DL-Sulforaphane
(R)-1-isothiocyanato-4-(methylsulfinyl)butane
Sulforaphane
(-)-Sulforaphane
L-Sulforaphane
4-isothiocyanatobutyl methyl (R)-sulfoxide
(R)-1-Isothiocyanato-4-(methylsulfinyl)butane,4-Methylsulfinylbutyl isothiocyanate
SCN4SO&1

Chemical & Physical Properties

[ Density]:
1.2±0.1 g/cm3

[ Boiling Point ]:
368.2±25.0 °C at 760 mmHg

[ Molecular Formula ]:
C6H11NOS2

[ Molecular Weight ]:
177.288

[ Flash Point ]:
176.5±23.2 °C

[ Exact Mass ]:
177.028198

[ PSA ]:
80.73000

[ LogP ]:
0.23

[ Vapour Pressure ]:
0.0±0.8 mmHg at 25°C

[ Index of Refraction ]:
1.567

[ Storage condition ]:
-20°C

MSDS

Click to get detail MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves

[ Hazard Codes ]:
Xi

[ Safety Phrases ]:
S22-S23-S24/25

[ RIDADR ]:
NONH for all modes of transport

[ HS Code ]:
2930909090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

  • 4-methylthiobutyl isothiocyanate
  • N-(4-methylsulfanyl-butyl)phthalimide
  • Carbon disulphide
  • 4-(METHYLTHIO)-1-BUTYLAMINE
  • Thiophosgene
  • (R)-4-(Methylsulfinyl)-1-butylamine

DownStream

Customs

[ HS Code ]: 2930909090

[ Summary ]:
2930909090. other organo-sulphur compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Articles

Sulforaphane prevents doxorubicin-induced oxidative stress and cell death in rat H9c2 cells.

Int. J. Mol. Med. 36 , 53-64, (2015)

Sulforaphane, a natural isothiocyanate compound found in cruciferous vegetables, has been shown to exert cardioprotective effects during ischemic heart injury. However, the effects of sulforaphane on ...

In vitro metabolic conversion of the organic breakdown products of glucosinolate to goitrogenic thiocyanate anion.

J. Sci. Food Agric. 95 , 2244-51, (2015)

Glucosinolates are abundant in Brassicaceae vegetables, and they are degraded into various organic breakdown products (BPs) (R-CN, -NCS and -SCN) by myrosinase when plant tissues are damaged. This stu...

Nrf2 Activation Promotes Keratinocyte Survival during Early Skin Carcinogenesis via Metabolic Alterations.

Cancer Res. 75 , 4817-29, (2015)

Pharmacologic activation of the transcription factor NRF2 has been suggested to offer a strategy for cancer prevention. In this study, we present evidence from murine tumorigenesis experiments suggest...


More Articles

Related Compounds

  • L-Sulforaphane
  • D,L-Sulforaphane-d8
  • D,L-Sulforaphane-L-cysteine
  • D,L-Sulforaphane Glutathione
  • D,L-Sulforaphane N-Acetyl-L-cysteine
  • D,L-Sulforaphane-d8 N-Acetyl-L-cysteine
  • 4-((Cyclohexylamino)methyl)benzoic acid hydrochloride
  • 1-[(2,4-Dichlorophenyl)methyl]-N-(1,1-dimethylethyl)-2-methyl-1H-indole-3-methanamine
  • 2-Methoxy-6-(pyrazol-1-yl)-benzonitrile
  • 1H-3-Benzazepin-7-ol, 8-chloro-2,3,4,5-tetrahydro-5-(3-iodophenyl)-3-methyl-, (S)-
  • (4-Methyl-tetrahydro-furan-2-yl)-methanol
  • N-(1-cyanocyclopentyl)-2-[4-(4-fluorobenzenesulfonyl)-1,4-diazepan-1-yl]acetamide
  • 4,5,6,7-Tetrahydrobenzo[d]isoxazole-3-carbaldehyde
  • tert-Butyl-DL-alanine
  • 4-amino-N-[2-tert-butyl-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-benzimidazol-5-yl]-N-ethylbenzenesulfonamide
  • N-[3-(Aminooxy)propyl]-N-butyl-1-butanamine