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

N-Acetyl-L-cysteine

Product Name
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
Formula Weight
163.19
MOL File
616-91-1.mol
More
Less

N-Acetyl-L-cysteine Property

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)
NIST Chemistry Reference
Acetylcysteine(616-91-1)
EPA Substance Registry System
L-Cysteine, N-acetyl- (616-91-1)
More
Less

Safety

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)
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H319Causes serious eye irritation

Precautionary statements

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

P337+P313IF eye irritation persists: Get medical advice/attention.

More
Less

N-Bromosuccinimide Price

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

N-Acetyl-L-cysteine Chemical Properties,Usage,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.

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.

N-Acetyl-L-cysteine Preparation Products And Raw materials

Raw materials

Preparation Products

More
Less

N-Acetyl-L-cysteine Suppliers

TCI Chemicals (India) Pvt. Ltd.
Tel
--
Fax
--
Email
sales-in@tcichemicals.com
Country
India
ProdList
6768
Advantage
58
Sisco Research Laboratories Pvt. Ltd.
Tel
--
Fax
--
Email
marketing@srlchem.com
Country
India
ProdList
4315
Advantage
58
A. B. Enterprises
Tel
--
Fax
--
Email
mlbang@rediffmail.com
Country
India
ProdList
1394
Advantage
58
Triveni chemicals
Tel
--
Fax
--
Email
sales@trivenichemical.com
Country
India
ProdList
6088
Advantage
58
Alfa Aesar
Tel
--
Fax
--
Email
tech@alfa.com
Country
India
ProdList
6905
Advantage
58
Pharma Affiliates
Tel
--
Fax
--
Email
@pharmaffiliates.com
Country
India
ProdList
6754
Advantage
58
MSC Chemicals
Tel
--
Fax
--
Country
India
ProdList
38
Advantage
58
Pluto International
Tel
--
Fax
--
Country
India
ProdList
57
Advantage
58
Argos International
Tel
--
Fax
--
Country
India
ProdList
154
Advantage
58
Grr Fine Chem/Grr Exports
Tel
--
Fax
--
Email
sunil@grrgroup.com
Country
India
ProdList
405
Advantage
58
Pharma Links
Tel
--
Fax
--
Email
info@pharmalinksindia.com
Country
India
ProdList
85
Advantage
58
Rushi Healthcare Pvt., Ltd.
Tel
--
Fax
--
Country
India
ProdList
50
Advantage
58
Chemfield Inc
Tel
--
Fax
--
Email
chemfieldinc@yahoo.in
Country
India
ProdList
24
Advantage
58
Clearsynth Labs
Tel
--
Fax
--
Email
fo@clearsynth.com
Country
India
ProdList
3887
Advantage
58
Beloor Bayir Biotech Limited
Tel
--
Fax
--
Email
ajaybairy@bayirextracts.com
Country
India
ProdList
19
Advantage
58
Hemarsh Technologies
Tel
--
Fax
--
Country
India
ProdList
23
Advantage
58
Arham Drugs And Chemicals Pvt., Ltd.
Tel
--
Fax
--
Email
sales1@arhamenterprise.net
Country
India
ProdList
22
Advantage
58
Innovative Health Care (India) Private Limited
Tel
--
Fax
--
Email
ihc.innovative@gmail.com
Country
India
ProdList
7
Advantage
58
Medi Pharma Drug House
Tel
--
Fax
--
Email
sales@medipharmadrughouse.com
Country
India
ProdList
81
Advantage
58
K P Manish Global Ingredients Private Limited
Tel
--
Fax
--
Email
info@kpmanish.com
Country
India
ProdList
36
Advantage
58
Aquatic Remedies Pvt., Ltd.
Tel
--
Fax
--
Email
kalpesh@aquaticgroup.in
Country
India
ProdList
93
Advantage
58
Olympus Chemicals & Fertilizers
Tel
--
Fax
--
Country
India
ProdList
486
Advantage
58
Amol Pharmaceuticals Pvt. Ltd. (US Pharma Lab)
Tel
--
Fax
--
Email
amol@amolpharmaceuticals.com
Country
India
ProdList
19
Advantage
58
Esschem Pvt., Ltd.
Tel
--
Fax
--
Email
esschem@vsnl.com
Country
India
ProdList
96
Advantage
58
Molychem
Tel
--
Fax
--
Country
India
ProdList
576
Advantage
58
Premier Drug House
Tel
--
Fax
--
Email
premierdrughouse@gmail.com
Country
India
ProdList
66
Advantage
58
Opulent Pharma
Tel
--
Fax
--
Country
India
ProdList
810
Advantage
58
Santo Righello Pvt. Ltd
Tel
--
Fax
--
Email
marketing@santorighello.com
Country
India
ProdList
918
Advantage
58
Kiran Lights Laboratories
Tel
--
Fax
--
Email
info@kiranlightlabs.com
Country
India
ProdList
262
Advantage
58
Pharmchem
Tel
--
Fax
--
Email
nipun@phrmchem.net
Country
India
ProdList
38
Advantage
58
Anant Pharmaceuticals Pvt. ltd
Tel
--
Fax
--
Email
info@anantlabs.com
Country
India
ProdList
736
Advantage
58
Placid Pharmachem
Tel
--
Fax
--
Email
parikshitjain@vsnl.com
Country
India
ProdList
115
Advantage
58
Lalchand Bhimraj Group
Tel
--
Fax
--
Email
info@lalchandbhimraj.com
Country
India
ProdList
50
Advantage
58
Planet Science (Quality Excipients)
Tel
--
Fax
--
Email
aparna@planetscience.in
Country
India
ProdList
55
Advantage
58
Shivam Pharma Chemicals
Tel
--
Fax
--
Email
info@shivampharma.com
Country
India
ProdList
656
Advantage
58
Cosmos Intenational
Tel
--
Fax
--
Email
jatin.nk@gmail.com
Country
India
ProdList
125
Advantage
58
Manus Aktteva Biopharma LLP
Tel
--
Fax
--
Country
India
ProdList
655
Advantage
58
Maas Pharma Chemicals
Tel
--
Fax
--
Email
info@maaspharmachemicals.com
Country
India
ProdList
1607
Advantage
58
Kemona Impex
Tel
--
Fax
--
Country
India
ProdList
221
Advantage
58
5 E Scientific
Tel
--
Fax
--
Email
milind@5escientific.com
Country
India
ProdList
136
Advantage
58
Brisben Chemicals
Tel
--
Fax
--
Country
India
ProdList
508
Advantage
58
SynZeal Research Pvt Ltd
Tel
--
Fax
--
Email
standards@synzeal.com
Country
India
ProdList
6514
Advantage
58
Amara Labs Private Limited
Tel
--
Fax
--
Email
Dharani@amaralabs.in
Country
India
ProdList
34
Advantage
58
Reax Chemicals
Tel
--
Fax
--
Country
India
ProdList
4217
Advantage
58
Anand Agencies
Tel
--
Fax
--
Email
en@gmail.com
Country
India
ProdList
2332
Advantage
58
Nakshatra Chemicals
Tel
--
Fax
--
Country
India
ProdList
162
Advantage
58
P.C. Chem India
Tel
--
Fax
--
Country
India
ProdList
134
Advantage
58
Globex Enterprises
Tel
--
Fax
--
Country
India
ProdList
44
Advantage
58
Otto Chemie Private Limited
Tel
--
Fax
--
Country
India
ProdList
76
Advantage
58
Nandlal Bankatlal Private Limited
Tel
--
Fax
--
Country
India
ProdList
30
Advantage
58
More
Less

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

Sichuan HongRi Pharma-Tech Co.,Ltd
Product
AC-L-Cys-OH 616-91-1
Price
US $0.00-0.00/kg
Min. Order
1kg
Purity
98%
Supply Ability
1T+
Release date
2023-12-29
WUHAN FORTUNA CHEMICAL CO., LTD
Product
N-Acetyl-L-cysteine 616-91-1
Price
US $0.00-0.00/Kg/Drum
Min. Order
1KG
Purity
98.0%-102%;USP
Supply Ability
500kg
Release date
2021-06-02
HEBEI SHENGSUAN CHEMICAL INDUSTRY CO.,LTD
Product
N-Acetyl-L-cysteine 616-91-1
Price
US $100.00-75.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
5000
Release date
2024-08-20

616-91-1, N-Acetyl-L-cysteineRelated Search:


  • (S)-ALPHA-AMINO-2-NAPHTHALENEPROPIONIC ACID
  • RARECHEM BK PT 0097
  • N-ACETYL CYSTEINE
  • N-ACETYL-3-MERCAPTOALANINE
  • N-ACETYL-L-(+)-CYSTEINE
  • N-ACETYL-L-CYSTEINE
  • N-ALPHA-ACETYL-L-CYSTEINE
  • AC-L-CYS-OH
  • ACETYLCYSTEINE
  • ACETYL-L-CYSTEINE
  • ACETYL-L-CYSTEINE, N-
  • ACC
  • AC-CYS-OH
  • MERCAPTURIC ACID
  • LNAL
  • LNAC
  • 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)
  • ACC1
  • Acetyl-CoA Carboxylase 1 human
  • acetyl-CoA carboxylase alpha
  • Anti-Acetyl-CoA Carboxylase, N-Terminal antibody produced in rabbit
  • Acetylcysteine Ph. Eur.
  • N-ACETYL-L-CYSTEIN extrapure for biochemistry
  • LNAC, NAC
  • N-Acetyl-L-cysteine Vetec(TM) reagent grade, 98%
  • Acetylcysteine Impurity
  • 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)
  • N-AC-L-Cys-OH
  • 3-(2-NAPHTHYL)-ALANINE
  • 2-L-NAPHTHYLALANINE
  • 2-ACETAMIDO-3-MERCAPTOPROPIONIC ACID
  • 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