S-Propylcysteine
Base Information
- Chemical Name: S-Propylcysteine
- CAS No.: 1115-93-1
Cost-effective and customizable S-Propylcysteine 1115-93-1 for sale
- Molecular Formula: C6H13NO2S
- Molecular Weight: 163.241
- Vapor Pressure: 0.000388mmHg at 25°C
- Refractive Index: 1.523
- Boiling Point: 294.748 °C at 760 mmHg
- Flash Point: 132.059 °C
- PSA： 88.62000
- Density: 1.164 g/cm3
- LogP: 1.24180
S-Propylcysteine(Cas 1115-93-1) Usage
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General Description |
S-Propylcysteine is a compound derived from cysteine, an amino acid found naturally in the body. It is commonly used in traditional medicine to support liver health, as it is believed to help protect the liver from damage caused by alcohol consumption and other toxins. S-Propylcysteine is also known for its antioxidant properties and is believed to help reduce oxidative stress in the body. Additionally, it may have anti-inflammatory effects and could potentially help support cardiovascular health. Overall, S-Propylcysteine is a promising compound with potential health benefits, particularly for liver and antioxidant support. |
InChI:InChI=1/C6H13NO2S/c1-2-3-10-4-5(7)6(8)9/h5H,2-4,7H2,1H3,(H,8,9)/t5-/m0/s1
1115-93-1 Relevant articles
S-carboxymethylcysteine synthase from Escherichia coli
Kumagai,Suzuki,Shigematsu,Tochikura
, p. 2481 - 2487 (1989)
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Acylase I-catalyzed deacetylation of N-acetyl-L-cysteine and S-alkyl-N- acetyl-L-cysteines
Uttamsing, Vinita,Keller,Anders
, p. 800 - 809 (1998)
The aminoacylase that catalyzes the hydr...
Role of allyl group in the hydroxyl and peroxyl radical scavenging activity of S-allylcysteine
Maldonado, Perla D.,Alvarez-Idaboy, J. Raúl,Aguilar-González, Adriana,Lira-Rocha, Alfonso,Jung-Cook, Helgi,Medina-Campos, Omar Noel,Pedraza-Chaverrí, José,Galano, Annia
, p. 13408 - 13417 (2011)
S-Allylcysteine (SAC) is the most abunda...
RELATION BETWEEN THE STRUCTURE OF ALLIIN ANALOGUES AND THEIR INHIBITORY EFFECT ON PLATELET AGGREGATION
Liakopoulou-Kyriakides, M.
, p. 1593 - 1594 (1985)
Key Word Index - Alliin; S-allyl-L-cyste...
Determination of S-methyl-, S-propyl-, and S-propenyl-L-cysteine sulfoxides by gas chromatography-mass spectrometry after tert-butyldimethylsilylation.
Tsuge, Kouichiro,Kataoka, Mieko,Seto, Yasuo
, p. 4445 - 4451 (2002)
A gas chromatographic-mass spectrometric...
Dynamic Kinetic Resolution for Asymmetric Synthesis of L-Noncanonical Amino Acids from D-Ser Using Tryptophan Synthase and Alanine Racemase
Yu, Jinhai,Li, Jing,Gao, Xia,Zeng, Shuiyun,Zhang, Hongjuan,Liu, Junzhong,Jiao, Qingcai
, p. 6618 - 6625 (2019/11/03)
L-Ser is often used to synthesize some s...
Unnatural amino acid synthesis by thermostable O-phospho-L-serine sulfhydrylase from hyperthermophilic archaeon Aeropyrum pernix K1
Nakamura, Takashi,Kunimoto, Kohei,Yuki, Toru,Ishikawa, Kazuhiko
supporting information, p. 1789 - 1792 (2017/11/23)
O-Acetyl-L-serine sulfhydrylase (OASS) f...
A step-by-step crystallization for preparing thio alkyl/alkenyl cysteine sulfoxide method
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Paragraph 0059; 0060, (2017/05/26)
The invention discloses a method for pre...
Transition metal complexes of S-Propyl-L-cysteine
Nazir, Shahbaz,Anwar, Jamil,Munawar, Munawar Ali,Best, Stephen Peter,Cheah, Michael,Nasir, Waqar,Bhatti, Amjad Ayub,Wichta, Peter
, p. 415 - 423 (2016/08/31)
Four transition metal complexes of the t...
1115-93-1 Process route
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-
52-90-4
L-Cysteine
-
-
106-94-5
propyl bromide
-
-
1115-93-1,65309-79-7,85955-34-6
S-propyl-L-cysteine
| Conditions | Yield |
|---|---|
|
With
triethylamine;
In
N,N-dimethyl-formamide;
|
65%
|
|
With
sodium hydroxide;
|
|
|
With
sodium hydroxide;
In
ethanol;
at 25 ℃;
for 0.05h;
|
3.3 g
|
|
L-Cysteine;
With
sodium hydroxide;
In
ethanol;
at 20 ℃;
for 0.166667h;
propyl bromide;
In
ethanol;
at 20 ℃;
for 6h;
|
75 g
|
-
-
52-89-1
l-cysteine hydrochloride
-
-
106-94-5
propyl bromide
-
-
1115-93-1,65309-79-7,85955-34-6
S-propyl-L-cysteine
| Conditions | Yield |
|---|---|
|
l-cysteine hydrochloride;
With
ethanol; sodium;
In
water;
for 0.583333h;
propyl bromide;
In
water;
for 1h;
|
70%
|
|
With
sodium hydroxide;
In
ethanol;
|
|
|
In
water;
at 4 ℃;
for 2h;
pH=5.5;
|
|
|
l-cysteine hydrochloride; propyl bromide;
With
ammonia;
In
water;
at 0 - 20 ℃;
With
acetic acid;
In
water;
|
1115-93-1 Upstream products
-
52-90-4
L-Cysteine
-
106-94-5
propyl bromide
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52-89-1
l-cysteine hydrochloride
-
107-03-9
1-thiopropane
1115-93-1 Downstream products
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14402-54-1
S-n-Propyl-N-acetyl-L-cysteine
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17795-24-3
(+/-)-S-propyl-L-cysteine sulfoxide
-
22812-90-4
2-hydroxyethyl ethyl sulfide
-
130603-69-9
2,4-Bis(propylthio)butanal