Product
Supplier
Encyclopedia
Inquiry
Home > Active Pharmaceutical Ingredients > Nervous System Drugs > Gabapentin for Sale > Antiepileptic Raw Material Gabapentin Powder CAS 60142-96-3
Antiepileptic Raw Material Gabapentin Powder CAS 60142-96-3 buy - large image1
Antiepileptic Raw Material Gabapentin Powder CAS 60142-96-3 buy - image1

Antiepileptic Raw Material Gabapentin Powder CAS 60142-96-3

GMP HALAL KOSHER ISO FDA 9 Inquiries

Unit Price: Get Latest Price
CAS No.:

60142-96-3

Grade:

Pharmaceutical Grade

Content:

99%

Packaging:

Foil Bag, Box, Drum

Sample Available:

Yes

Price valid (until):

2022-12-31

Company Type:
Manufactory
Location:
China
Payment Terms:
TT against copy of documents
Average Lead Time:
8 days
Qualification:
Main Products:

Herb Extracts,Cosmetic raw materails,API

  • Product Description

  • Seller Information

  • Inquiry History

  • Description

    Antiepileptic Raw Material Gabapentin Powder CAS 60142-96-3
    Product Name
    Gabapentin
    Specification
    99%
    CAS60142-96-3
    Molecular Formula
    C9H17NO2
    Molecular Weight
    171.24




    Antiepileptic Raw Material Gabapentin Powder CAS 60142-96-3

    Gabapentin is used to treat epilepsy. It's also taken for nerve pain. Nerve pain can be caused by different illnesses, including diabetes and shingles, or it can happen after an injury. Occasionally, Gabapentin cas 60142-96-3 is used to treat migraine headaches.
    Gabapentin is structurally similar to GABA (sc-203053; γ-aminobutyric acid) and is reported in various research studies to increase GABA concentrations within the brain. Gabapentin is also noted to bind to a novel site on voltage-sensitive Ca2+ channels. Additionally, Gabapentin is reported to demonstrate inhibition of dopamine release from caudate nucleus, preventneuronal cell death, and is antinociceptive.


    ECHEMI Editorial Reference
    Gabapentin (Neurontin) is a pharmaceutical drug, specifically a GABA analog. It was originally developed to treat epilepsy, and currently is also used to relieve neuropathic pain.IC50 Value: 140 nM (α2δ subunit of calcium channel) [1]Target: Calcium Channelin vitro: Gabapentin, baclofen and CGP 44532 all reduced the electrically stimulated release of [3H]glutamic acid (IC50=20 microM, 0.8 microM and 2 microM, respectively). Gabapentin was without effect on the release of [3H]GABA, whilst
    Solid
    Gabapentin is a gamma-amino acid that is cyclohexane substituted at position 1 by aminomethyl and carboxymethyl groups. Used for treatment of neuropathic pain and restless legs syndrome. It has a role as an anticonvulsant, a calcium channel blocker, an environmental contaminant and a xenobiotic. It derives from a gamma-aminobutyric acid.|Gabapentin is a structural analogue of the inhibitory neurotransmitter gamma-aminobutyric acid ([GABA]) that was first approved for use in the United States in 1993. It was originally developed as a novel anti-epileptic for the treatment of certain types of seizures - today it is also widely used to treat neuropathic pain. Gabapentin has some stark advantages as compared with other anti-epileptics, such as a relatively benign adverse effect profile, wide therapeutic index, and lack of appreciable metabolism making it unlikely to participate in pharmacokinetic drug interactions.. It is structurally and functionally related to another GABA derivative, [pregabalin].|Gabapentin is an Anti-epileptic Agent. The physiologic effect of gabapentin is by means of Decreased Central Nervous System Disorganized Electrical Activity.|Gabapentin is a unique anticonvulsant that is used as adjunctive therapy in management of epilepsy and for neuropathic pain syndromes. Therapy with gabapentin is not associated with serum aminotransferase elevations, but several cases of clinically apparent liver injury from gabapentin have been reported.|Gabapentin is a synthetic analogue of the neurotransmitter gamma-aminobutyric acid with anticonvulsant activity. Although its exact mechanism of action is unknown, gabapentin appears to inhibit excitatory neuron activity. This agent also exhibits analgesic properties. (NCI04)|A cyclohexane-gamma-aminobutyric acid derivative that is used for the treatment of PARTIAL SEIZURES; NEURALGIA; and RESTLESS LEGS SYNDROME.

    Certificates

    Basic Info
    Product Name:

    Gabapentin

    Other Name:

    Cyclohexaneacetic acid,1-(aminomethyl)-;1-(Aminomethyl)cyclohexaneacetic acid;Gabapentin;CI 945;Go 3450;GOE 2450;Neurontin;GOE 3450;Gabapen;Bexal;Gabamox;Generis;2-[1-(Aminomethyl)cyclohexyl]acetic acid;Conventin;Neuronyin;Neuril;Convalis;Gabarone;Gralise;Nupentin;Fanatrex;Sigma G 154;(1-Aminomethyl-cyclohexyl)-acetic acid

    CAS No.:

    60142-96-3

    Molecular Formula:

    C9H17NO2

    InChIKeys:

    InChIKey=UGJMXCAKCUNAIE-UHFFFAOYSA-N

    Molecular Weight:

    171.24

    Exact Mass:

    171.24

    EC Number:

    262-076-3

    UNII:

    6CW7F3G59X

    NSC Number:

    742194

    DSSTox ID:

    DTXSID0020074

    NCI Thesaurus Code:

    C1108

    Color/Form:

    White to off-white crystalline solid; crystals from ethanol/ether

    ATC Code:

    N03AX12|N - Nervous system

    HScode:

    2922499990

    Categories:

    Nervous System Drugs

    Characteristics
    PSA:

    63.32000

    XLogP3:

    1.19

    Appearance:

    off-white solid

    Density:

    1.1±0.1 g/cm3

    Melting Point:

    162-166 °C

    Boiling Point:

    314.4±15.0 °C at 760 mmHg

    Flash Point:

    9℃

    Refractive Index:

    1.489

    Water Solubility:

    H2O: 10 mg/mL

    Storage Conditions:

    Desiccate at +4°C

    Vapor Pressure:

    2.94X10-10 mm Hg at 25 deg c (est)

    Taste:

    Bitter

    PKA:

    3.7None

    Henrys Law Constant:

    Henry's Law constant = 9.32X10-12 atm-cu m/mol at 25 °C (est)

    Dissociation Constants:

    3.7|pKa1 = 3.68 at 25 °C (carboxylic acid); pKa2 = 10.70 (primary amine)

    Collision Cross Section:

    138.6 Ų [M+H]+ [CCS Type: TW, Method: calibrated with polyalanine and drug standards]|139.7 Ų [M+H]+

    Experimental Properties:

    Isoelectric point = 7.14|Hydroxyl radical reaction rate constant = 4.01X10-11 cu cm/molecule-sec at 25 °C (est)

    Hazard Identification

    Classification of the substance or mixture

    Skin irritation, Category 2

    Eye irritation, Category 2

    Specific target organ toxicity – single exposure, Category 3

    Reproductive toxicity, Category 1B

    GHS label elements, including precautionary statements

    Pictogram(s)
    Signal word

    Danger

    Hazard statement(s)

    H315 Causes skin irritation

    H319 Causes serious eye irritation

    H335 May cause respiratory irritation

    H360 May damage fertility or the unborn child

    Precautionary statement(s)
    Prevention

    P264 Wash ... thoroughly after handling.

    P280 Wear protective gloves/protective clothing/eye protection/face protection/hearing protection/...

    P261 Avoid breathing dust/fume/gas/mist/vapours/spray.

    P271 Use only outdoors or in a well-ventilated area.

    P203 Obtain, read and follow all safety instructions before use.

    Response

    P302+P352 IF ON SKIN: Wash with plenty of water/...

    P321 Specific treatment (see ... on this label).

    P332+P317 If skin irritation occurs: Get medical help.

    P362+P364 Take off contaminated clothing and wash it before reuse.

    P305+P351+P338 IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing.

    P304+P340 IF INHALED: Remove person to fresh air and keep comfortable for breathing.

    P319 Get medical help if you feel unwell.

    P318 IF exposed or concerned, get medical advice.

    Storage

    P403+P233 Store in a well-ventilated place. Keep container tightly closed.

    P405 Store locked up.

    Disposal

    P501 Dispose of contents/container to an appropriate treatment and disposal facility in accordance with applicable laws and regulations, and product characteristics at time of disposal.

    Other hazards which do not result in classification

    no data available

    Handling and Storage

    Precautions for safe handling

    Handling in a well ventilated place. Wear suitable protective clothing. Avoid contact with skin and eyes. Avoid formation of dust and aerosols. Use non-sparking tools. Prevent fire caused by electrostatic discharge steam.

    Conditions for safe storage, including any incompatibilities

    Keep container tightly closed in a dry and well-ventilated place.

  • Seller Information
    Business Type:

    Manufactory

    Main Products:

    Herb Extracts,Cosmetic raw materails,API

    Location:

    1403,Jinye B Block

    Payment Terms:

    TT against copy of documents

    Average lead Time:

    8 days

    Total Annual Revenue:

    $2.5 million-$5 million

    Total Employees:

    11-50

    Year of Establishment:

    2015

    Xian ZB Biotech Co.,Ltd is a leading Manufactory supplier of Arbutin, Nicotinamide, Flucytosine based in Xi'an, Shaanxi, China. With a commitment to quality and customer satisfaction, Xian ZB Biotech Co.,Ltd has become a trusted name in the industry. Our product line includes a range of high-quality Arbutin, Nicotinamide, Flucytosine, which are available at competitive prices. Xian ZB Biotech Co.,Ltd has established itself as a reliable supplier of chemical products on the echemi.com.

  • Inquiry History
    9 Inquiries
    Country Product Purchase Quantity Date Posted
    Saudi Arabia

    Gabapentin Powder

    500 G Sep 4, 2026
    United States

    Gabapentin

    1 KG Jul 17, 2026
    Sri Lanka

    Gabapentin USP 47 / USP 48

    2000 KG Jun 19, 2026
    United States

    Gabapentin

    100 G Oct 21, 2025
    United States

    Gabapentin

    1 KG Jul 24, 2025
    India

    Gabapentin

    300 KG Jan 26, 2025
    India

    Gabapentin

    1 MT Jun 27, 2024
    India

    Gabapentin hydrochloride

    1 KG Dec 30, 2025
    United States

    Gabapentin powder

    1 KG Oct 25, 2024
    Post an enquiry for this product
pic ×

Scan the QR Code to Share

All products displayed on this website are only for non-medical purposes such as industrial applications or scientific research, and cannot be used for clinical diagnosis or treatment of humans or animals. They are not medicinal or edible.

According to relevant laws and regulations and the regulations of this website, units or individuals who purchase hazardous materials should obtain valid qualifications and qualification conditions.

The information shown above is provided by the enterprise itself, and the authenticity, accuracy and legitimacy of the content are the responsibility of the publishing company. ECHEMI does not bear any guarantee responsibility for this. Please be aware that risks in internet transactions objectively exist.

Feedback & Suggestions
Send Message

Thank you for your feedback. If you require further assistance, please contact us by email at info@echemi.com or call us at +86-532-55729510.