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Home > Encyclopedia > L-Ascorbic acid

L-Ascorbic acid

pharmaceutical raw materials
L-Ascorbic acid structure

L-Ascorbic acid 

structure
  • CAS No:

    50-81-7

  • Formula:

    C6H8O6

  • Chemical Name:

    L-Ascorbic acid

  • Synonyms:

    L-Ascorbic acid;Allercorb;Antiscorbic vitamin;Antiscorbutic vitamin;Ascorbajen;Ascorin;Ascorteal;Ascorvit;Cantan;Cantaxin;Catavin C;Cebicure;Cebione;Cecon;Cegiolan;Ceglion;Celin;Ce-Mi-Lin;Cenetone;Cereon;Cergona;Cescorbat;Cetemican;Cevalin;Cevatine;Cevex;Cevimin;Ce-Vi-Sol;Cevitamic acid;Cevitamin;Cevitan;Cevitex;Ciamin;Cipca;Concemin;Davitamon C;3-keto-L-Gulofuranolactone;L-3-Keto-threo-hexuronic acid lactone;Laroscorbine;Lemascorb;Liqui-Cee;3-Oxo-L-gulofuranolactone;Planavit C;Proscorbin;C-Quin;Ribena;Secorbate;Vicelat;Vicin;Vitacimin;Vitacin;Vitamin C;Vitamisin;Vitascorbol;Redoxon;Vitacee;L-threo-Hex-2-enonic acid,γ-lactone;Ascorbic acid;L-Lyxoascorbic acid;Xyloascorbic acid,L-;Cevital;L-Xyloascorbic acid;C-Vimin;Testascorbic;Adenex;Hybrin;Cetamid;Colascor;Scorbu C;Xitix;Celaskon;Cebion;Cemagyl;Ascorbutina;Viforcit;Vitace;IDO-C;Viscorin;Ascoltin;Hicee;Neo-Valdrin;(+)-Ascorbic acid;Citrovit;Chewcee;L-threo-Ascorbic acid;Ronotec 100;L-(+)-Ascorbic acid;Rontex 100;Juvamine;Rovimix C;Vasc;P 1110;VC 97;Kangbingfeng;Suncoat VC 40;Viscorin 100M;Cewin;Ceklin;Ascorbicap;Cetane;Cetane-Caps TC;Cetebe;E 300;NSC 218455;NSC 33832;Cell C;Ascorell;C-L 6/PW;VC 40;100M;Cinal;Rovimix C-EC;Vitashure 160;Cevarol;Tanvimil C;Vaginorm-C;Monovitan C;Pascorbin;Ascorbalox;Energil C;Bovi-C;Emvit-C;Novasol Cof;5-(1,2-Dihydroxyethyl)-3,4-dihydroxy-5H-furan-2-one;14536-17-5;30208-61-8;50976-75-5;56172-55-5;56533-05-2;57304-74-2;57606-40-3;88845-26-5;89924-69-6;129940-97-2;154170-90-8;259133-78-3;623158-95-2;882690-91-7;884381-69-5;885512-24-3;896436-13-8;1018124-03-2;1129294-89-8;1428525-25-0;1703051-92-6

  • Categories:

    Cosmetic Ingredient  >  Antioxidant Ingredient

Description

L-Ascorbic acid is an effective reducing agent and donor antioxidant.

L-Ascorbic acid Basic Attributes

176.124

176.12

200-066-2

29362700

Characteristics

107.22

-1.4074

White to very light yellow crystalline powder

1.65 g/cm3

190-192 °C (decomp)

415.8ºC at 760 mmHg

180.4ºC

21 ° (C=10, H2O)

H2O: 333 g/L (20 ºC)

Ventilation low temperature drying

9.28X10-11 mm Hg at 25 deg C (est)

LD50 oral in rat: 11900mg/kg

[α]D/20 between + 20,5° and + 21,5° (10 % w/v aqueous solution)

Dust forms explosible mixtures in air with moderate explosion severity.

Odorless

Pleasant, sharp, acidic taste

Between 2,4 and 2,8 (2 % aqueous solution)

4.7(at 10 °C)

Safety Information

NONH for all modes of transport

1

R20/21/22

S24/25

CI7650000

Xn

Separated from strong oxidants and strong bases.

Stable. May be weakly light or air sensitive. Incompatible with oxidizing agents, alkalies, iron, copper.

P264, P280, P302+P352, P305+P351+P338, P321, P332+P313, P337+P313, P362

H315

L-Ascorbic acid Use and Manufacturing

Methods of Manufacturing

Glucose is hydrogenated to N-sorbitol under the catalysis of nickel and then fermented with acetic acid mold at 30 to 34 ° C and Ph value of 5.2 to 5.5 to form L-sorbose. In the presence of fuming sulfuric acid and -8 ℃, L-sorbose and acetone condensation of diacetone sorbose; in the nickel sulfate catalytic and 75 ~ 80 ℃, and then sodium hypochlorite oxidation to produce diacetone-2-keto-L , Gulonic acid; finally hydrolyzed under acidic conditions to produce 2-keto-L-gulonic acid; and then get ascorbic acid.

Uses

1. Antiscorbutic, antiviral
2. Analgesic, antipyretic
3. Physiological antioxidant. Coenzyme for a number of hydroxylation reactions; required for collagen synthesis. Widely distributed in plants and animals. Inadequate intake results in deficiency syndromes such as scurvy. Used as antimicrobial and antioxidant in foodstuffs.

Computed Properties

Molecular Weight:176.12
XLogP3:-1.6
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:2
Exact Mass:176.03208797
Monoisotopic Mass:176.03208797
Topological Polar Surface Area:107
Heavy Atom Count:12
Complexity:232
Defined Atom Stereocenter Count:2
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

Price Analysis

Make your L-Ascorbic acid purchase based on the price and market insights! ECHEMI provides professional market insights with prices for you to make a better choice. Learn more on L-Ascorbic acid prices .
  • Data: 2026-08-13
  • Price: 19.00Yuan/kg
  • Change: 0

Drug Function and Efficacy

It participates in amino acid metabolism, synthesis of neurotransmitters, synthesis of collagen and tissue cell interstitial, can reduce the permeability of capillaries, accelerate blood coagulation, stimulate coagulation function, promote iron absorption in the intestine, promote the decrease of blood lipids, increase resistance to infection, participate in detoxification function, and has antihistamine effect and prevents the formation of carcinogens (nitrosamines).

This ingredient has been used in drugs with the following functions (note: it does not mean that the ingredient itself has the following health functions)

Related Drugs

Registered Holders

  • ANMOL CHEMICALS PRIVATE LTD

    United States United States
    Active
  • Amoli Organics Pvt Ltd

    United States United States
    Active
  • MCGUFF PHARMACEUTICALS INC

    United States United States
    Active

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