L-Ascorbic acid
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L-Ascorbic acid
structure -
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CAS No:
50-81-7
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Formula:
C6H8O6
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Chemical Name:
L-Ascorbic acid
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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
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CAS No:
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
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.
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
- 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).
Registered Holders
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ANMOL CHEMICALS PRIVATE LTD
Active
United States
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Amoli Organics Pvt Ltd
Active
United States
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MCGUFF PHARMACEUTICALS INC
Active
United States
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Business licensedTrader Supplier of Sodium benzoate,Potassium sorbate,Xanthan gum,phosphoric acid,citric acidInquiryUnit Price: $3-3.3 /KG FOBCAS No.: 50-81-7Grade: Food Grade Cosmetic Grade Medicine GradeContent: 99%
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