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ChemicalBook >> CAS DataBase List >>N-Acetyl-L-cysteine

N-Acetyl-L-cysteine

CAS No.
616-91-1
Chemical Name:
N-Acetyl-L-cysteine
Synonyms
ACETYLCYSTEINE;N-ACETYL CYSTEINE;ACC;Acetylcystein;H-2-NAL-OH;AC-CYS-OH;ACETYL-L-CYSTEINE;AC-L-CYS-OH;H-NAL-OH;2-ACETAMIDO-3-MERCAPTOPROPIONIC ACID
CBNumber:
CB2127503
Molecular Formula:
C5H9NO3S
Molecular Weight:
163.19
MDL Number:
MFCD00004880
MOL File:
616-91-1.mol
MSDS File:
SDS
Last updated:2024-12-18 14:07:02

N-Acetyl-L-cysteine Properties

Melting point 106-108 °C(lit.)
alpha -35.1 ºC (c=2,H2O)
Boiling point 407.7±40.0 °C(Predicted)
Density 1.249 (estimate)
vapor pressure 0Pa at 20℃
refractive index 24 ° (C=JPC Method)
storage temp. 2-8°C
solubility H2O: 100 mg/mL with heating
pka pK1: 9.52 (30°C)
form Solid
color White
Water Solubility Soluble in water, ethanol, methanol, dimethyl sulfoxide, hot isopropyl alcohol, methyl acetate and ethyl acetate. Insoluble in chloroform and ether.
Merck 14,88
BRN 1724426
Stability Stable. Incompatible with strong oxidizing agents.
InChIKey PWKSKIMOESPYIA-BYPYZUCNSA-N
LogP -0.6 at 23℃
CAS DataBase Reference 616-91-1(CAS DataBase Reference)
EWG's Food Scores 1
NCI Dictionary of Cancer Terms acetylcysteine; N-acetylcysteine; N-acetyl-L-cysteine
FDA UNII WYQ7N0BPYC
NIST Chemistry Reference Acetylcysteine(616-91-1)
NCI Drug Dictionary acetylcysteine
ATC code R05CB01,S01XA08,V03AB23
EPA Substance Registry System L-Cysteine, N-acetyl- (616-91-1)

Pharmacokinetic data

Protein binding 50%
Excreted unchanged in urine 20-30%
Volume of distribution 0.33-0.47(L/kg)
Biological half-life 2-6 / -

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H319
Precautionary statements  P264-P280-P305+P351+P338-P337+P313
Risk Statements  36/37/38
Safety Statements  22-24/25
WGK Germany  3
RTECS  HA1660000
10-23
TSCA  Yes
HS Code  29309016
Hazardous Substances Data 616-91-1(Hazardous Substances Data)
Toxicity LD50 orally in rats: 5050 mg/kg (Goldenthal)
NFPA 704
0
1 0

N-Acetyl-L-cysteine price More Price(92)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich SAB4501395 Anti-Acetyl-CoA Carboxylase, N-Terminal antibody produced in rabbit affinity isolated antibody 616-91-1 100μG $506 2024-03-01 Buy
Sigma-Aldrich BP907 Acetylcysteine British Pharmacopoeia (BP) Reference Standard 616-91-1 200MG $262 2024-03-01 Buy
Sigma-Aldrich A8199 N-Acetyl-L-cysteine BioXtra, ≥99% (TLC) 616-91-1 1KG $2390 2024-03-01 Buy
Sigma-Aldrich A7250 N-Acetyl-L-cysteine Sigma Grade, ≥99% (TLC), powder 616-91-1 1kg $1040 2024-03-01 Buy
Sigma-Aldrich 1009005 Acetylcysteine United States Pharmacopeia (USP) Reference Standard 616-91-1 200mg $436 2024-03-01 Buy
Product number Packaging Price Buy
SAB4501395 100μG $506 Buy
BP907 200MG $262 Buy
A8199 1KG $2390 Buy
A7250 1kg $1040 Buy
1009005 200mg $436 Buy

N-Acetyl-L-cysteine Chemical Properties,Uses,Production

Description

N-Acetyl-L-cysteine is an N-acetylated derivative of cysteine, which contains a sulfhydryl group in the molecule, which can break the disulfide bond (-S-S-) of the mucin peptide bond, so that the mucin chain becomes a small molecule peptide chain, reducing The viscosity of mucin, so It is a dissolving drug for mucus in mucus, purulent sputum and respiratory tract.

Chemical Properties

N-Acetyl-L-cysteine is a white crystalline powder that has a garlic-like smell and sour taste. It is hygroscopic, and can dissolve in water or ethanol, but is insoluble in ether and chloroform. This substance is also acidic in aqueous solution, with a pH range of 2-2.75 for a concentration of 10g/L H2O.

Originator

Mucomyst ,Mead Johnson,US

Uses

A metabolite of Methyl Isocyanate.
N-Acetyl-L-cysteine, by itself a poor scavenger of oxidants, is converted inside cells to yield sulfane sulfur species, which are very potent scavengers of oxidants.

Uses

An antioxidant mucolytic acetylated amino acid.
N-acetyl-l-cysteine (NAC) is a derivative of the dietary amino acid l-cysteine. NAC has a high affinity for lung tissue, which it supports through mucolytic and antioxidant action. NAC also enhances glutathione production and plays a role in heavy metal detoxification.

Definition

ChEBI: N-Acetyl-L-cysteine is an N-acetyl-L-amino acid that is the N-acetylated derivative of the natural amino acid L-cysteine. It is a pharma ceutical drug and nutritional supplement used primarily as a mucolytic agent and in the management of paracetamol (acetaminophen) overdose. Other uses include sulfate repletion in conditions, such as autism, where cysteine and related sulfur amino acids may be depleted.

Manufacturing Process

To a suspension of 35.2 grams (0.2 mol) of L-cysteine hydrochloride monohydrate stirred in a reaction vessel containing 87 ml of 91% aqueous tetrahydrofuran under a nitrogen atmosphere there is added 54.4 grams (0.4 mol) of sodium acetate trihydrate. The mixture is stirred for 20 minutes at room temperature to insure neutralization of the hydrochloride salt resulting in the formation of a suspension of equimolar amounts of cysteine and sodium acetate.
The mixture is then chilled to 3-6°C by external cooling and 20 ml (20.8 grams, 0.21 mol) of acetic anhydride is added thereto in dropwise fashion with cooling in the above range. The resulting mobile suspension is stirred for 6 hours at room temperature, allowed to stand overnight, and finally heated at reflux (72°C) for 4 hours. The resulting suspension of sodium N-acetyl-Lcysteinate is then neutralized by treatment at 5-10°C with 8 grams of hydrogen chloride. Resulting sodium chloride is removed by filtration and the product is isolated by distilling the solvent from the filtrate in vacuum and crystallizing the residue from 35 ml of water, yield 26.3 grams (80.6%) of Nacetylcysteine as a white solid, MP 109-110°C.

brand name

Acetadote (Cumberland); Mucomyst (Apothecon); Mucosil (Dey).

Therapeutic Function

Expectorant

benefits

n-acetyl-l-cysteine is a skin conditioner. It may also be used as an anti-aging ingredient given a demonstrated ability to regulate skin atrophy and reduce the appearance of fine lines and wrinkles.

General Description

N-Acetyl-L-cysteine is the N-acetyl derivative of the amino acid Lcysteine, and is a precursor in the formation of the antioxidant glutathione in the body. The thiol (sulfhydryl) group confers antioxidant effects and is able to reduce free radicals. This compound is sold as a dietary supplement commonly claiming antioxidant and liver protecting effects. It is used as a cough medicine because it breaks disulfide bonds in mucus and liquefies it, making it easier to cough up. It is also this action of breaking disulfide bonds that makes it useful in thinning the abnormally thick mucus in cystic and pulmonary fibrosis patients. In India it is marketed by Intas under the trade name 'Efetil'.

Biochem/physiol Actions

Antioxidant and mucolytic agent. Increases cellular pools of free radical scavengers. Reported to prevent apoptosis in neuronal cells but induce apoptosis in smooth muscle cells. Inhibits HIV replication. May serve as a substrate for microsomal glutathione transferase.

Mechanism of action

N-Acetyl-L-cysteine is a kind of membrane penetrating antioxidant. It has anti-inflammatory activity through regulating the activation of NF-KB and HIF-1α; as well as modulation of ROS. It can penetrate across the membrane, replenishes intracellular and glutathione and GSH to help the cell fight against oxidative stress. In addition to its antioxidant action, NAC acts as a vasodilator by facilitating the production and action of nitric oxide. This property is an important mechanism of action in the prophylaxis of contrast-induced nephropathy and the potentiation of nitrate-induced vasodilation (Millea 2009).

Side effects

At dosages of 1,200 mg twice daily or lower, N-acetylcysteine is well tolerated. At these dosages, side effects are unusual, but may include nausea, vomiting, diarrhea, transient skin rash, flushing, epigastric pain, and constipation.
www.aafp.org

Safety Profile

Poison by intraperitoneal route. Moderately toxic by other routes. Mutation data reported. When heated to decomposition it emits very toxic fumes of NO, and SOx,

Synthesis

Acetylcysteine, N-acetyl-L-cysteine (23.2.4), is synthesized by reacting L-cysteine hydrochloride with acetic anhydride in the presence of sodium acetate.

Synthesis_616-91-1

Veterinary Drugs and Treatments

N-Acetyl-L-cysteine is a mucolytic agent that can be used to stop the melting effect of collagenases and proteases on the cornea. It is useful in halting melting through inhibition of metalloproteinases, but is not felt to be useful for melting caused by infectious agents.

Metabolism

N-Acetyl-L-cysteine undergoes transformation in the liver, and may be present in plasma as the parent compound or as various oxidised metabolites such as N-acetylcystine, N,N-diacetylcystine, and cysteine either free or bound to plasma proteins. Oral bioavailability is low (4-10%). It has been suggested that N-Acetyl-L-cysteine's low oral bioavailability may be due to metabolism in the gut wall and first-pass metabolism in the liver.

storage

Store at -20°C

References

http://www.sigmaaldrich.com/catalog/product/sigma/a0737?lang=en&region=US
Grinberg, L, et al. "N-acetylcysteine amide, a novel cell-permeating thiol, restores cellular glutathione and protects human red blood cells from oxidative stress." Free Radical Biology & Medicine 38.1(2005):136-145.
Zhang, Xinsheng, et al. "N-Acetylcysteine Amide Protects Against Methamphetamine-Induced Oxidative Stress and Neurotoxicity in Immortalized Human Brain Endothelial Cells." Brain Research1275(2009):87-95.
Penugonda, S, et al. "Effects of N-acetylcysteine amide (NACA), a novel thiol antioxidant against glutamate-induced cytotoxicity in neuronal cell line PC12."Brain Research 1056.2(2005):132.
Lee, Kyung Sun, et al. "A novel thiol compound, N-acetylcysteine amide, attenuates allergic airway disease by regulating activation of NF-|[kappa]|B and hypoxia-inducible factor-1|[alpha]|." Experimental & Molecular Medicine 39.6(2007):756.

Global( 1100)Suppliers
Supplier Tel Email Country ProdList Advantage
DONBOO AMINO ACID COMPANY
+8613063595538 donboo@donboo.com China 9363 58
Xi'an Kono chem co., Ltd.,
029-86107037 13289246953 info@konochemical.com China 1169 58
BOC Sciences
16314854226; +16314854226 inquiry@bocsci.com United States 19741 58
Wuhan Haorong Biotechnology Co.,ltd
+86-18565342920; +8618565342920 sales@chembj.net China 289 58
Leading Chemical and Trading Co.,Ltd
+8615669938129 sales@leadingchemical.com China 130 58
Shandong Hanjiang Chemical Co., Ltd
+86-0533-2066820 +8618369939125 hanson@sdhanjiang.com China 998 58
Wuhan Fortuna Chemical Co., Ltd
+86-027-59207850 info@fortunachem.com China 5975 58
Guangzhou Tosun Pharmaceutical Ltd
+86-020-61855200-902 +8618124244216 info@upharm.cn China 831 58
Hebei Weibang Biotechnology Co., Ltd
+8615531157085 abby@weibangbio.com China 8810 58
XI'AN TIANGUANGYUAN BIOTECH CO., LTD.
+86-029-86333380 18829239519 sales06@tgybio.com China 901 58

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View Lastest Price from N-Acetyl-L-cysteine manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
N-Acetyl-L-cysteine pictures 2024-12-22 N-Acetyl-L-cysteine
616-91-1
US $100.00-75.00 / kg 1kg 99% 5000 HEBEI SHENGSUAN CHEMICAL INDUSTRY CO.,LTD
AC-L-Cys-OH pictures 2024-12-20 AC-L-Cys-OH
616-91-1
US $0.00-0.00 / kg 1kg 98% 1T+ Sichuan HongRi Pharma-Tech Co.,Ltd
N-Acetyl-L-Cysteine pictures 2024-12-20 N-Acetyl-L-Cysteine
616-91-1
US $120.00 / kg 1kg 99% 20ton Hebei Zhuanglai Chemical Trading Co.,Ltd
  • AC-L-Cys-OH pictures
  • AC-L-Cys-OH
    616-91-1
  • US $0.00-0.00 / kg
  • 98%
  • Sichuan HongRi Pharma-Tech Co.,Ltd
(S)-ALPHA-AMINO-2-NAPHTHALENEPROPIONIC ACID RARECHEM BK PT 0097 N-ACETYL-L-(+)-CYSTEINE N-ACETYL-L-CYSTEINE N-ALPHA-ACETYL-L-CYSTEINE ACETYL-L-CYSTEINE, N- LNAL L-Cysteine,N-acetyl- Mercapturic acid, (R)- Muco sanigen Mucocedyl mucofilin Mucolator Mucolyticum Mucolyticum Lappe mucolyticumlappe mucolyticum-lappe Mucolytikum Lappe mucolytikumlappe Mucomyst Mucosolvin Mucret N-Ac-L-cysteine N-alpha-Actetyl-L-cysteine N-Acetyl-L-Cysteine(NAC) Acetyl-CoA Carboxylase 1 human acetyl-CoA carboxylase alpha Anti-Acetyl-CoA Carboxylase, N-Terminal antibody produced in rabbit N-ACETYL-L-CYSTEIN extrapure for biochemistry LNAC, NAC N-Acetyl-L-cysteine Vetec(TM) reagent grade, 98% Acetylcysteine IMP N-ACETYL-L-CYSTEINE BIOXTRA N-ACETYL-L-CYSTEINE CELL CULTURE TES (R)-2-Acetamido-3-mercaptopropionic acid Acetyl-L-cysteine≥ 99% (Titration) Acetyl-L-cysteineUSP (Non-animal source, Manufactured as per GMP) , 98.0-102.0% (Assay) 2-L-NAPHTHYLALANINE N-ACETYL-L-CYSTEINE SIGMAULTRA N-ACETYL-L-CYSTEINE CELL CULTURE TESTED N-ACETYL-L-CYSTEINE SIGMA GRADE N-Acetyl-L-CysteineForBiochemistry N-Acetyl-L-CysteineUsp24 N-Acetyl-L-cysteine,98+% (S)-N-Acetylcysteine Cysteine, N-acetyl-, L- (6CI, 8CI) Fluibiotic Fluimicil N-Acetyl-(R)-cysteine N-Acetyl-L-cysteine;Tixair;NAC;Mucret;Neo-Fluimucil L-α-Acetamido-β-mercaptopropionic acid ACETYLCYSTEINE,USP Acetyl-N-cysteine ACETYLCYSTEINE (N-ACETYL-L-CYSTEINE) Parvolex Respaire Tixair N-Acetyl-L-cysteine ,99%